Patent application title: SEROLOGICAL MARKERS FOR DETECTING COLORECTAL CANCER AND THEIR APPLICATION FOR INHIBITING COLORECTAL CANCER CELLS
Inventors:
Err-Cheng Chan (Tao-Yuan, TW)
Kuei-Tien Chen (Tao-Yuan, TW)
Jau-Song Yu (Tao-Yuan, TW)
Yu-Sun Chang (Tao-Yuan, TW)
Jinn-Shiun Chen (Taoyuan, TW)
IPC8 Class: AG01N33574FI
USPC Class:
435 74
Class name: Measuring or testing process involving enzymes or micro-organisms; composition or test strip therefore; processes of forming such composition or test strip involving antigen-antibody binding, specific binding protein assay or specific ligand-receptor binding assay to identify an enzyme or isoenzyme
Publication date: 2013-04-04
Patent application number: 20130084582
Abstract:
Embodiments relate to serological markers for detecting the colorectal
cancer and applications of the serological markers. A phospholipid
scramblase1 (PLSCR1), a stomatin-like protein 2 (STOML2) or a transport
protein Sec61β (SEC61β) increases expression in the blood at
the earlier stage of the colorectal cancer. Detecting the expression of
the PLSCR1, STOML2 or SEC61β protein or an induced autoantibody of
each protein in a blood sample is used to diagnose the colorectal cancer.
Moreover, the serological marker improves the detection efficiency and
the sensitivity in detecting the colorectal cancer and is used to predict
the prognosis. The serological markers are applied in preparing a
detection device or inhibiting the growth of the colorectal cancer cells.Claims:
1. A serological marker for detecting a colorectal cancer, at least
comprising a phospholipid scramblase 1 (PLSCR1), the phospholipid
scramblase 1 protein being significant increased in blood samples of
colorectal cancer patients and having an amino acid sequence has
similarity more than 90% with following sequence
TABLE-US-00010
10 20 30 40 50 60
MDKQNSQMNA SHPETNLPVG YPPQYPPTAF QGPPGYSGYP GPQVSYPPPP AGHSGPGPAG
70 80 90 100 110 120
FPVPNQPVYN QPVYNQPVGA AGVPWMPAPQ PPLNCPPGLE YLSQIDQILI HQQIELLEVL
130 140 150 160 170 180
TGFETNNKYE IKNSFGQRVY FAAEDTDCCT RNCCGPSRPF TLRIIDNMGQ EVITLERPLR
190 200 210 220 230 240
CSSCCCPCCL QEIEIQAPPG VPIGYVIQTW HPCLPKFTIQ NEKREDVLKI SGPCVVCSCC
250 260 270 280 290 300
GDVDFEIKSL DEQCVVGKIS KHWTGILREA FTDADNFGIQ FPLDLDVKMK AVMIGACFLI
310
DFMFFESTGS QEQKSGVW
2. The serological marker as claimed in claim 1, wherein the serological marker further comprises a SEC61.beta. protein or a STOML2 protein.
3. The serological marker as claimed in claim 1, wherein the serological marker further comprises at least one antigen of a protein that is selected from a group consists of: RPH3AL, RPL36, STOML2, P53, Survivin, ANXA4 and SEC61.beta..
4. The serological marker as claimed in claim 1, wherein the serological marker further comprises an autoantibody of a protein that is selected from a group consists of: PLSCR1, STOML2, and SEC61.beta..
5. The serological marker as claimed in claim 1, wherein the PLSCR1 protein increases expression in the blood sample at an earlier stage of the colorectal cancer.
6. The serological marker as claimed in claim 2, wherein the STOML2, or the SEC61.beta. protein increases expression in the blood sample at an earlier stage of the colorectal cancer.
7. The serological marker as claimed in claim 4, wherein the autoantibody of PLSCR1, STOML2 or SEC61.beta. increases expression in the blood sample at an earlier stage of the colorectal cancer.
8. A method for detecting a colorectal cancer, comprising steps of establishing a database comprises multiple normal blood samples collected from multiple healthy controls that is confirmed by a clinically medical diagnosis, each blood sample at least has a value of expression of phospholipid scramblase 1 (PLSCR1), the expression values are used to calculate a cutoff value; collecting a blood sample from a volunteer; detecting a PLSCR1 protein expression of the tested blood sample; and comparing the PLSCR1 protein expression of the tested blood sample with the cutoff value, a positive result is defined as the PLSCR1 protein expression of the tested blood sample is higher than the cutoff value and has highly risk be the colorectal cancer.
9. The method as claimed in claim 8, wherein the database further comprises the expression level or the autoantibody response of a protein selected from the group consist of: a STOML2 and a SEC61.beta., and the tested blood sample is detected the expression of the STOML2 protein or the SEC61.beta. protein, and the autoantibody response of the STOML2 protein or the SEC61.beta. protein.
10. The method as claimed in claim 8, wherein the step of detecting a PLSCR1 expression of the tested blood sample uses an immunoassay.
11. The method as claimed in claim 9, wherein the expression level or the autoantibody response of the STOML2 protein or the SEC61.beta. protein is detected by an immunoassay.
12. A detection device for detecting a colorectal cancer, comprising a sample container is used to contain a blood sample; a reagent at least comprises an antibody of a phospholipid scramblase 1 (PLSCR1) protein; and a substrate is provided for developing a signal.
13. The detection device as claimed in claim 12, wherein the reagent further comprises an antibody or a recombinant protein of a protein selected from a group consist of: a STOML2 protein or a SEC61.beta. protein.
14. The detection device as claimed in claim 12, wherein the detection device further comprises a database stores multiple normal blood samples collected from multiple healthy controls that is confirmed by a clinically medical diagnosis, each blood sample at least has an expression value of a phospholipid scramblase 1 (PLSCR1) protein, the multiple expression values are used to calculate a cutoff value.
15. The detection device as claimed in claim 13, wherein the detection device further comprises a database stores multiple normal blood samples collected from multiple healthy controls that is confirmed by a clinically medical diagnosis, each blood sample at least has an expression value of a STOML2 protein or a SEC61.beta. protein, the expression values are used to calculate a cutoff value.
16. The detection device as claimed in claim 12, wherein the reagent further comprises a protein selected from a group consist of a STOML2 protein and a SEC61.beta. protein.
17. The detection device as claimed in claim 12, wherein the reagent further comprises a antibody of a protein selected from a group consist of PLSCR1, STOML2 and SEC61.beta..
18. The detection device as claimed in claim 12, wherein the reagent further comprises an antigen selected from a group consist of RPH3AL, RPL36, STOML2, P53, Survivin, ANXA4 and SEC61.beta..
19. A detection device for detecting a colorectal cancer, comprising a sample container is used to contain a blood sample; a reagent at least comprises a recombinant protein of phospholipid scramblase 1 (PLSCR1) protein; and a substrate is provided for developing a signal.
20. The detection device as claimed in claim 19, wherein the reagent further comprises an antibody or a recombinant protein of a protein selected from a group consists of: STOML2 and SEC61.beta..
21. The detection device as claimed in claim 19, wherein the detection device further comprises a database stores multiple normal blood samples collected from multiple healthy controls that is confirmed by a clinically medical diagnosis, each blood sample at least has a value of autoantibody response of phospholipid scramblase 1 (PLSCR1) protein, the values of autoantibody response are used to calculate a cutoff value.
22. The detection device as claimed in claim 20, wherein the detection device further comprises a database stores multiple normal blood samples collected from multiple healthy controls that is confirmed by a clinically medical diagnosis, each blood sample at least has a value of autoantibody response of a STOML2 protein or a SEC61.beta. protein, the values of autoantibody response are used to calculate a cutoff value.
23. The detection device as claimed in claim 22, wherein the reagent further comprises a protein selected from a group consists of a STOML2 protein and a SEC61.beta. protein.
24. The detection device as claimed in claim 22, wherein the reagent further comprises an antibody of a protein selected from a group consist of PLSCR1 protein, STOML2 protein and SEC61.beta. protein.
25. The detection device as claimed in claim 22, wherein the reagent further comprises an antigen selected from a group consist of RPH3AL, RPL36, STOML2, P53, Survivin, ANXA4 and SEC61.beta..
26. A method for inhibiting the growth of colorectal cancer cells, comprising steps of preparing an anti-phospholipid scramblase 1 (PLSCR1) antibody; and reacting the anti-PLSCR1 antibody with the colorectal cancer cells.
27. The method as claimed in claim 26, wherein the anti-PLSCR1 antibody is formed as an injection, a tablet or a powder, used in the therapy of colorectal cancer.
28. A serological marker for detecting a colorectal cancer, at least comprising a SEC61.beta. protein being significant increased in the blood samples of the colorectal cancer patients and having an amino acid sequence has similarity more than 90% with following sequence TABLE-US-00011 10 20 30 40 50 60 MPGPTPSGTN VGSSGRSPSK AVAARAAGST VRQRKNASCG TRSAGRTTSA GTGGMWRFYT 70 80 90 EDSPGLKVGP VPVLVMSLLF IASVFMLHIW GKYTRS
29. The serological marker as claimed in claim 28, wherein the serological marker further comprises a phosphoholipid scramblase 1 (PLSCR1) protein or a STOML2 protein.
30. The serological marker as claimed in claim 28, wherein the serological marker further comprises at least one antigen of a protein that is selected from a group consists of: RPH3AL, RPL36, STOML2, P53, Survivin and ANXA4.
31. The serological marker as claimed in claim 28, wherein the serological marker further comprises an autoantibody of a protein that is selected from a group consists of: PLSCR1, STOML2, and SEC61.beta..
32. The serological marker as claimed in claim 28, wherein the SEC61.beta. protein increases expression in the blood sample at an earlier stage of the colorectal cancer.
33. The serological marker as claimed in claim 29, wherein the PLSCR1 protein or the STOML2 protein increases expression in the blood sample at an earlier stage of the colorectal cancer.
34. The serological marker as claimed in claim 31, wherein the autoantibody of the PLSCR1 protein, STOML2 protein or the SEC61.beta. protein increases expression in the blood sample at an earlier stage of the colorectal cancer.
35. A serological marker for detecting a colorectal cancer, at least comprising an STOML2 protein being significant increased in the blood samples of the colorectal cancer patients and having an amino acid sequence has similarity more than 90% with following sequence TABLE-US-00012 10 20 30 40 50 60 MLARAARGTG ALLLRGSLLA SGRAPRRASS GLPRNTVVLF VPQQEAWVVE RMGRFHRILE 70 80 90 100 110 120 PGLNILIPVL DRIRYVQSLK EIVINVPEQS AVTLDNVTLQ IDGVLYLRIM DPYKASYGVE 130 140 150 160 170 180 DPEYAVTQLA QTTMRSELGK L5LDKVFRER ESLNASIV DAINQAADCWGI RCLRYEIKDI 190 200 210 220 230 240 HVPPRVKESM QMQVEAERRK RATVLESEGT RESAINVAEG KKQAQILASE AEKAEQINQA 250 260 270 280 290 300 AGEASAVLAK AKAKAEAIRI LAAALTQHNG DAAASLTVAE QYVSAFSKLA KDSNTILLPS 310 320 330 340 350 NPGDVTSMVA QAMGVYGALT KAPVPGTPDS LSSGSSRDVQ GTDASLDEEL DRVKMS
36. The serological marker as claimed in claim 35, wherein the serological marker further comprises phosphoholipid scramblase 1 (PLSCR1) or a SEC61.beta. protein.
37. The serological marker as claimed in claim 35, wherein the serological marker further comprises at least one antigen of a protein that is selected from a group consists of: RPH3AL, RPL36, P53, Survivin, ANXA4 and SEC61.beta..
38. The serological marker as claimed in claim 35, wherein the serological marker further comprises an autoantibody of a protein that is selected from a group consists of: PLSCR1, STOML2, and SEC61.beta..
39. The serological marker as claimed in claim 35, wherein the STOML2 protein increases expression in the blood sample at an earlier stage of the colorectal cancer.
40. The serological marker as claimed in claim 36, wherein the PLSCR1, or the SEC61.beta. protein increases expression in the blood sample at an earlier stage of the colorectal cancer.
41. The serological marker as claimed in claim 38, wherein the autoantibody of the PLSCR1 protein, the STOML2 protein or the SEC61.beta. protein increases response level in the blood sample at an earlier stage of the colorectal cancer.
Description:
FIELD OF THE INVENTION
[0001] Embodiments relate to serological markers for detecting colorectal cancer and a method for using the serological markers, especially to a serological marker for detecting colorectal cancer and a method for using the serological marker with high sensitivity and specificity. Further, embodiments relate to the capability of colorectal cancer inhibition by neutralizing the function of selected serological markers.
BACKGROUND OF THE INVENTION
[0002] Cancers are shown as the major causes of death. Earlier detecting of cancer, inhibiting the development and spread of cancer cells, and even researching a method for preventing cancer cells are major issues focused by researchers and the public.
[0003] Colorectal cancer (CRC) has been the third common cancer among all cancers. Every year, there are a million new cases and 500,000 people death due to the colorectal cancer. Researches reveal earlier detection and diagnosis will help to decrease the mortality and morbidity of colorectal cancer.
[0004] Screening methods currently available for detecting the colorectal cancer include digital rectal examination, fecal occult blood test (FOBT), sigmoidoscopy, and colonoscopy. Although above-mentioned methods have improved the detection efficiency of the colorectal cancer, however, their diagnostic value as a general screening tool is limited because of poor sensitivity and a high falsepositive rate (FOBT), costs, risks, and inconvenience (colonoscopy). To overcome these problems, the development of novel biomarkers that can allow for the early detection of CRC is crucial.
[0005] The advancement of molecular biology, proteomic and preventive medicine provide more useful information or tools to increase the proceeding of develop a novel detection or therapy for colorectal cancer. A biomarker revealing overexpression in tumor tissues (i.e. a tumor tissue or a tissue biopsy) by using one of above-mentioned methods might not release to the circulation of the blood, show a large amount of expression in the blood, or has a long half-life to be detected. A carcinoembryonic antigen (CEA), a clinically established serological marker, is a marker currently widely used in colorectal cancer detection but is always suggested to be used in estimating the prognosis of CRC patients due to the limited sensitivity and specificity.
[0006] Accordingly, using different biotechnological methods to search and develop a biomarker to earlier diagnosis the colorectal cancer and to improve the therapeutic efficiency is very important
SUMMARY OF THE INVENTION
[0007] According to one aspect of an embodiment of the invention, a serological marker for detecting a colorectal cancer with high sensitivity and specificity at least comprises a phospholipid scramblase 1 (PLSCR1) protein. The PLCSR1 is highly expressed in colorectal cancer patients. Therefore, the colorectal cancer is easy to be determined the possibility and risk by collecting and assaying the PLSCR1 expression in a blood sample instead of invasive obtaining a biopsy. The PLSCR1 protein is increased in the blood at the earlier stage of the colorectal cancer so that the PLSCR1 protein could be applied in the early detection of the colorectal cancer. In an embodiment, the PLSCR1 protein is combined with other proteins, such as SEC61β or STOML2 protein, that are sensitive and specific with the colorectal cancer to improve the detection efficiency.
[0008] According to another aspect of an embodiment of the invention, a method for detecting the colorectal cancer comprises steps of establishing a database, collecting a blood sample, detecting a serological marker in the blood sample and comparing the serological maker expression with the database.
[0009] According to yet another aspect of an embodiment of the invention, a detection device comprises a sample container, at least a PLSCR1 protein antibody and a substrate. A blood sample is collected and applied in the detection device to test the expression of a serological marker, which is compared with a database to determine the possibility of the colorectal cancer.
[0010] Due to the highly sensitivity and specificity to the colorectal cancer, an antigen of the PLSCR1 is used to as a serological marker in detecting the colorectal cancer, and the PLSCR1 or a recombinant protein of PLSCR1 is applied in a detection device for detecting the colorectal cancer. Otherwise, an antibody neutralizing the function of selected serological marker has capability to inhibiting the cell growth of the colorectal cancer.
[0011] The above objects and advantages of the present invention will become more readily apparent to those ordinarily skilled in the art after reviewing the following detailed descriptions and accompanying drawings in which:
BRIEF DESCRIPTIONS OF THE DRAWINGS
[0012] The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
[0013] FIG. 1 shows the expression of PLSCR1 protein in colorectal cancer tissues and normal tissues;
[0014] FIG. 2 shows the expression of PLSCR1 protein in blood samples of colorectal cancer patients and healthy controls;
[0015] FIG. 3A is a photograph showing the expression of PLSCR1 protein in a normal tissue (normal colorectal mucosa);
[0016] FIG. 3B is a photograph showing the expression of PLSCR1 protein in a benign colorectal polyp tissue;
[0017] FIG. 3C is a photograph showing the expression of PLSCR1 protein in a colorectal adenocarcinoma tissue;
[0018] FIG. 4 shows the detection efficiency of PLSCR1 protein, the current used CEA marker and a combination of both markers;
[0019] FIG. 5. shows a relationship between the PLSCR1 expression and the overall survival rate of the colorectal cancer patients;
[0020] FIG. 6. shows an in vitro inhibition of the colorectal cancer cell growth by treating with a PLSCR1 antibody;
[0021] FIG. 7. shows an in vivo inhibition of the colorectal cancer by treating with a PLSCR1 antibody;
[0022] FIG. 8. shows the expression of SEC61β protein in the colorectal cancer tissues and the matching normal tissues;
[0023] FIG. 9. shows the SEC61β autoantibody response in blood samples of colorectal cancer patients and healthy controls;
[0024] FIG. 10. shows the SEC61β autoantibody response at different stages of the colorectal cancer;
[0025] FIG. 11. shows the detection efficiency of the SEC61β autoantibody, the current used CEA marker and a combination of both markers;
[0026] FIG. 12. shows the expression of STOML2 protein in blood samples of colorectal cancer patients and healthy controls;
[0027] FIG. 13. shows the detection efficiency of STOML2 protein, the current used CEA marker and a combination of both markers;
[0028] FIG. 14. shows the STOML2 autoantibody response in blood samples of colorectal cancer patients and healthy controls; and
[0029] FIG. 15. shows the STOML2 autoantibody response in different cancers.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
Embodiment 1
Screening and Selecting a Serological Marker for Detecting the Colorectal Cancer
[0030] The embodiment selects a phospholipid scramblase 1 (PLSCR1) as a serological marker for detecting the colorectal cancer. The PLSCR1 is overexpressed in the colorectal cancer tissue and is tested the efficiency as a serological marker to detect the colorectal cancer.
[0031] 28 colorectal cancer patients are enrolled. A colorectal cancer tissue (tumor tissue) and a normal tissue away from the colorectal cancer tissue for at least 10 centimeters collected from each patient is respectively analyzed the proteomic profile. All tissues are cut into small pieces, washed by using 0.9% sodium chloride to remove blood, homogenized in STM solution (5 ml STM solution/g tissue, 0.25 M sucrose, 10 mM Tris(hydroxymethyl)aminomethane hydrochloride (Tris-HCl) and 1 mM magnesium chloride) to form a homogenous solution.
[0032] The homogenous solution is centrifuged at 260×g for 5 minutes to remove the precipitated nuclei and tissue debris. A separated supernatant solution is further centrifuged at 1500×g for 10 minutes to precipitate the crude membrane proteins. The crude membrane proteins are homogenized in two-thirds volume of the original homogenate volume (contains 0.25M STM solution and protease inhibitor) and centrifuged at 16000×g for an hour to purify the membrane proteins. The membrane pellet is washed by 0.1M sodium carbonate for overnight and is centrifuged at 16000×g for an hour to re-collect the membrane proteins. The purified membrane proteins are homogenized in 90% formic acid and stored in -80° C.
[0033] The purified membrane proteins are resuspended in 6M urea, 5 mM ethylene diamine tetraacetic acid (EDTA), and 2% sodium dodecyl sulfate (SDS) in 0.1M triethylammonium bicarbonate (TEABC) and sonicated at 4 for 10 minutes. A bovine serum albumin (BSA) is used as an internal standard (0.1% BSA in the purified membrane proteins). The purified membrane proteins were reduced by 5 mM Tris(2-carboxyethyl)-phosphine (TCEP) and alkylated by 2 mM methyl methanethiosulfonate (MMTS) at room temperature for 30 min. A 40% acrylamide solution (acrylamide: bisacrylamide is 29:1, v/v), 10% (w/v) ammonium persulfate (APS) and 100% N,N,N',N'-Tetramethylethylenediamine (TEMED) are added to the purified membrane protein mixture to polymerize as a gel.
[0034] The gel is cut into small pieces and subjected to tryptic digestion in 25 mM TEABC solution at 37° C. to form peptides. The peptides are extracted from the gel using sequential extraction with 25 mM TEABC, 0.1% (v/v) trifluoroacetic acid (TFA) in water, 0.1% TFA in acetonitrile (ACN), and 100% ACN. The extracted peptides are concentrated, desalted and analyzed by a liquid chromatography-tandem mass spectrometry (LC-MS/MS).
[0035] Information collected from LC-MS/MS is searched by Mascot v2.2 against International Protein Index (IPI) human database from the European Bioinformatics Institute. The selection constraints: (a) only tryptic peptides with up to two missed cleavage sites were allowed; and (b) 0.3-Da mass tolerances for MS and 0.1-Da mass tolerances for MS/MS fragment ions. Only unique peptides with scores ≧35 (p<0.05) were confidently assigned. The amino acid sequence of enrolled peptide is further compared to identify the corresponding protein.
[0036] Results from the LC-MS/MS analysis are used to compare the expression of a specific protein in the colorectal cancer tissue (tumor tissue) and the normal tissue. For example, peak area of protein A in the colorectal cancer tissue and the normal tissue is R1 and R2 respectively. The peak area of the internal standard in the colorectal cancer tissue and the normal tissue is S1 and S2 respectively. Comparing the ratio of the protein A and the internal standard in the colorectal cancer tissue and the normal tissue, a difference in abundance of 1.5-fold to indicate a statistically significance of higher or lower expression, respectively.
[0037] PLSCR 1 is selected from the LC-MS/MS analysis due to the significant overexpression in the colorectal cancer tissue than the matching normal tissue, and is further tested the expression in the western blotting assay and the immunohistochemistry (IHC) assay.
[0038] Western Blotting Analysis
[0039] The colorectal cancer tissue and the matching normal tissue are suspended in a lysis buffer (0.25 M sucrose, 10 mM Tris-HCl, pH 7.6, 1 mM MgCl2, 1% SDS) with protease inhibitor mixture (20 μg/μL aprotinin, 20 μg/μL leupeptin, and 1 mmol/L phenylmethanesulfonyl fluoride (PMSF); protein:protein inhibitor was 100:1, v/v) and homogenized on ice to form a protein suspension. 40 μg of protein suspension was subjected to the western blot analysis.
[0040] With reference to Table 1, Table 1 illustrates the expression of the PLSCR1 in the colorectal cancer tissue compared with their normal counterpart. 18 of 28 paired tissues show at least 1.5 folds overexpression in the colorectal cancer tissue compared with their normal counterpart.
TABLE-US-00001 TABLE 1 The expression of the PLSCR1 in the colorectal cancer tissue compared with their normal counterpart. No. Fold (colorectal cancer tissue/normal tissue) 1 1.92 2 3.91 3 4.02 4 0.90 5 1.38 6 0.98 7 4.03 8 2.88 9 2.13 10 3.04 11 0.85 12 2.16 13 1.09 14 1.09 15 12.59 16 11.85 17 10.87 18 2.86 19 6.33 20 1.37 21 2.04 22 2.17 23 1.40 24 0.98 25 8.85 26 0.72 27 6.62 28 5.19
[0041] The PLSCR1 of the embodiment has an UniProt accession number O15162 with sequence shows as following:
TABLE-US-00002 10 20 30 40 50 60 MDKQNSQMNA SHPETNLPVG YPPQYPPTAF QGPPGYSGYP GPQVSYPPPP AGHSGPGPAG 70 80 90 100 110 120 FPVPNQPVYN QPVYNQPVGA AGVPWMPAPQ PPLNCPPGLE YLSQIDQILI HQQIELLEVL 130 140 150 160 170 180 TGFETNNKYE IKNSFGQRVY FAAEDTDCCT RNCCGPSRPF TLRIIDNMGQ EVITLERPLR 190 200 210 220 230 240 CSSCCCPCCL QEIEIQAPPG VPIGYVIQTW HPCLPKFTIQ NEKREDVLKI SGPCVVCSCC 250 260 270 280 290 300 GDVDFEIKSL DEQCVVGKIS KHWTGILREA FTDADNFGIQ FPLDLDVKMK AVMIGACFLI 310 DFMFFESTGS QEQKSGVW
[0042] However, one of ordinary skill in the art will realize that any sequence has more than 90% similarity with above-mentioned sequence is capable to apply in the present invention.
[0043] In order to understand whether the PLSCR 1 is significant presented in a blood specimen or has capability to be a serological marker, blood samples respectively from colorectal patients and healthy controls are collected and electrophoresised to separate proteins in blood samples by SDS-PAGE. Proteins in the SDS-PAGE are transferred to a polyvinylidene fluoride (PVDF) membrane. The PVDF membrane is blocked with 5% skim milk in Tris-buffered saline-Tween buffer (25 mmol/L Tris, 190 mmol/L NaCl, and 0.5% [v/v] Tween 20, pH 7.5) and then incubated with primary rabbit antihuman PLSCR1 polyclonal antibody (1:1000 dilution) at 4° C., overnight. After being washed, the membranes were incubated at 25° C. for 1 h with peroxidase-conjugated mouse antirabbit IgG antibody (1:5000 dilution), and then were developed with a chemiluminescence reagent kit and photographed. Immunoblot images were analyzed by an Imagemaster analyser, and the band intensities are presented in arbitrary units (AU).
[0044] With reference to FIGS. 1 to 3C, respectively show the PLSCR1 expression in the colorectal tissues and blood samples from CRC patients or healthy volunteers. For the tissue samples, the western blot assay shows the PLSCR1 expression in the colorectal cancer tissue and in the normal tissue is 63.2±41 and 29±28.1 AU (p<0.001), respectively. The PLSCR1 expression is at least two folds in the colorectal cancer tissue than in the normal tissue. The IHC assay shows the PLSCR 1 expression increases with the malignant grade of the colorectal cancer in the tissue biopsy. For the blood samples, the western blot assay shows the PLSCR1 is significant expression in the blood samples of the colorectal cancer patients (44 AU) than in the healthy controls (18.5 AU). Therefore, the PLSCR1 has potential to be a serological marker to detect the colorectal cancer.
[0045] One of ordinary skill in the art realizes the western blot assay for detecting the PLSCR1 expression might be replaced by an immunoassay such as an enzyme linked immunosorbent assay (ELISA).
[0046] One of ordinary skill in the art also obviously understands when the PLSCR1 is highly expressed in the colorectal cancer, a corresponding antibody (autoantibody) induced by the PLSCR1 will be increased. Therefore, the autoantibody of PLSCR1 is able to be a serological marker for detecting the colorectal cancer.
[0047] Specificity and sensitivity of the PLSCR1 for detecting the colorectal cancer
[0048] With reference to FIG. 4 and Table 2, show the comparison between the PLSCR1 and a current used CEA marker.
TABLE-US-00003 TABLE 2 Sensitivity of CEA and PLSCR1 in CRC patients with different stage. Sensitivity Stage of the Numbers Combined colorectal cancer of sample CEAa (A) PLSCR1b (B) (A) + (B) Early stage 25 4 (16%) 20 (80%) 20 (80%) Advanced stage 34 18 (53%) 27 (79%) 30 (88%) All CRC patients 59 22 (37%) 47 (80%) 50 (85%) aCutoff value ≧5 ng/mL. bCutoff value ≧13.9 AU.
[0049] The PLSCR1 alone has better detection efficiency while applying in detecting the early stage and advanced stage colorectal of cancer than the CEA does. The overall detection rate of the PLSCR1 is at least 2 folds than the CEA so that the PLSCR1 has great capability for detecting the colorectal cancer. Moreover, combination of the PLSCR1 and the CEA will increase the efficiency in CRC detection.
[0050] Relationship between the PLSCR1 expression and the overall survival rate
[0051] With reference to FIG. 5, a Cox proportional hazards model is applied to evaluate the relationship between the PLSCR1 expression and the overall survival rate. The CRC patients were divided into two groups (high PLSCR1 and low PLSCR1) according to a cutoff point of the IHC SI value (SI) by 1. Patients in low PLSCR1 group have longer survival period of 49.8 months than in high PLSCR1 group of 39.2 months. The PLSCR1 expression and the overall survival rate obviously exists a significant relationship.
[0052] Further, an anti-PLSCR1 antibody that is produced from the PLSCR1 of the embodiment is used to be identified the capability of CRC inhibition in a mouse model. The anti-PLSCR1 antibody is directly contacted with a colorectal cancer HT29 cells. With reference to FIG. 6, the MTT (3-(4,5-cimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) assay shows the anti-PLSCR1 antibody with concentration more than 0.35 μg/well (μg/mL) is able to inhibit the colorectal cancer cells after two days.
[0053] With reference to FIG. 7, after transplanting the HT29 cells (1×106 cells) to the subcutaneous region of female nude mice (7 weeks old) for 29 days, respectively injecting an affinity purified anti-PLSCR1 monoclonal antibody (+PLSCR1Ab) or an IgG (PLSCR1 Ab) into the mice every two days for 6 days. The anti-PLSCR1 monoclonal antibody significantly inhibits the growth of HT29 cells, but same dose of IgG does not effect the growth of HT29 cells. While observing an H&E staining of the colorectal cancer tissue, the amount of the cancer cells of the colorectal cancer tissue decreases after the mice treated with the anti-PLSCR1 monoclonal antibody. Therefore, the anti-PLSCR1 monoclonal antibody affects and inhibits the cell growth both in vitro and in vivo.
[0054] Table 3 shows selected proteins by using the above mentioned methods which might has potential to be colorectal cancer detection markers. The markers are overexpressed in at least 20 tissue pairs from a total of 28 colorectal tissue pairs.
TABLE-US-00004 TABLE 3 Proteins have potential to be colorectal cancer detection markers. No. of Patients CRC celllinec with Expressed in Large COLO Protein Upregulation Locationa CRC Tissueb Intestinec 205 HCT-116 HCT-15 HT29 KM-12 SW-620 CEACAM5 25 PM x x x STOML2 24 PM x x x x x x x CEACAM6 24 PM x DEFA1 24 Extracellular x region RPL36 23 Cytoplasm x x x x x x TSPO 23 OM x x x x x x x x OCIAD2 22 OM x x x x x x IKIP 22 OM CYBA 22 PM x x x x x x x GOLT1B 22 OM x x x x x x x ELA2 22 Extracellular region CYB5B 21 OM x x x x x x x SEC61B 21 OM x x x x x x TOMM40 21 OM x x x x x x TMEM63A 21 PM x x x x x TSPAN8 21 PM x x x x x x x SLC16A3 21 PM x x x x x x x x LAMP1 21 OM x x x x x x x ANXA4 21 PM x x x x x x x x TOMM5 21 Unknown x x x x x x x x SLC2A1 20 PM x x x x x x TMCO1 20 OM x x x x x x OPRS1 20 PM x x x x x x x athe location is annontated by Gene Onotology and Ingenuity Pathway Analysis Knowledge Base. PM indicates plasma membrane and OM indicates organelle membrane bthe expression of proteins in colorectal cancer tissues are obtained in Human Protein Reference Database cthe data are obtained from Ingenuity Pathway Analysis
[0055] Accordingly, the PLSCR1 is able to be applied in manufacturing a detection device for detecting the colorectal cancer. The detection device comprises a sample container, at least an anti-PLSCR1 antibody and a substrate. Blood samples are collected and applied in the sample container, and reacts with the anti-PLSCR1 antibody. The substrate might a chromophoric reagent or a fluorescence reagent that is combined with another anti-PLSCR1 antibody and develop a signal related to the binding between the PLSCR1 and the anti-PLSCR1 antibody, which is compared with a database or a cutoff value. The database collects the values of PLSCR1 expression from healthy controls. The cutoff value is calculated by estimating the values of PLSCR1 expression from healthy controls.
Embodiment 2
The Capability of a SEC61β Protein as a Serological Marker for Detecting Colorectal Cancer
[0056] This embodiment uses a SEC61β protein listed in the Table 3 or an autoantibody induced from the SEC61β protein as a marker to detect the colorectal cancer.
[0057] In this embodiment, a comparison of SEC61β expression between the colorectal cancer tissue and the matching normal tissue is established by using western blot assay. Differences between the embodiment 1 and 2 shows as following:
[0058] The colorectal cancer tissue and the matching normal tissue is respectively mixed with an electrophoresis buffer contains 2% SDS and 5% 2-mercaptoethanol and heated at 100° C. for 5 minutes. Proteins in the tissues are fractioned by a 12% denatured polyacrylamide gel and then are transferred to the PVDF membrane. The PVDF membrane is blocked with 5% skim milk. Proteins in the PVDF membrane react with a rabbit anti-human SEC61β polyclonal antibody at room temperature for 2 hours and then react with a peroxide-conjugated second antibody at room temperature for 1 hour.
[0059] The SEC61β of the embodiment has an UniProt accession number P60468 with sequence shows as following:
TABLE-US-00005 10 20 30 40 50 60 MPGPTPSGTN VGSSGRSPSK AVAARAAGST VRQRKNASCG TRSAGRTTSA GTGGMWRFYT 70 80 90 EDSPGLKVGP VPVLVMSLLF IASVFMLHIW GKYTRS
[0060] However, one of ordinary skill in the art will realize that any sequence has more than 90% similarity with above-mentioned sequence is capable to apply in the present invention.
[0061] With reference to FIG. 8, the western blot assay indicates that the SEC61 expression in the colorectal cancer tissue is higher than in the normal tissue. A similar result is also shown in an IHC assay.
[0062] With reference to FIGS. 9 and 10, shows a relationship between the autoantibody induced from the SEC61β and the colorectal cancer. In the blood samples of colorectal cancer patients, the expression of SEC61β autoantibody is higher than in the blood samples of healthy controls. Also, in the earlier stage of the colorectal cancer, the SEC61β autoantibody in the blood is significantly increased.
[0063] With reference to FIG. 11 and Table 4, shows a comparison of the detection efficiency between the SEC61β autoantibody and the current used CEA marker. The SEC61β autoantibody has the sensitivity and the specificity in detection the colorectal cancer by 79% and 75% respectively, whereas for CEA, these values were 40% and 87%, respectively. Combination of the SEC61β autoantibody and the CEA marker show a higher detection capacity than either marker alone (AUC=0.838).
TABLE-US-00006 TABLE 4 A comparison of the detection efficiency in the colorectal cancer between the SEC61β autoantibody and the current used CEA marker. Sample anti-SEC61βantibody CEA anti-SEC61βantibody + CEA Source No. positive negative P value positive negative P value positive negative P value Patient 86 68 (79%) 18 (21%) <0.001 34 (40%) 52 (60%) <0.001 61 (71%) 25 (29%) <0.001 Healthy 72 18 (25%) 54 (75%) 9 (13%) 63 (87%) 8 (11%) 64 (89%) volunteer
[0064] With reference to Table 5, shows the detection efficiency of the SEC61β autoantibody and the current used CEA in detecting CRC patients with different stages. The SEC61β autoantibody has great capability to detect the colorectal cancer in early stage and has detection efficiency more than 75%.
TABLE-US-00007 TABLE 5 The detection efficiency of the SEC61β autoantibody and the current used CEA in CRC patients with different stages Sample CEA SEC61β autoantibody CEA + Stage of CRC No. positive positive SEC61β I 10 0 (0%) 8 (80%) 7 (70%) II 25 11 (44%) 19 (76%) 18 (72%) I + II 35 11 (31%) 27 (77%) 25 (71%) III 35 12 (34%) 29 (83%) 26 (74%) IV 16 11 (69%) 12 (75%) 10 (63%) III + IV 51 23 (45%) 41 (80%) 36 (71%) All 86 34 (40%) 68 (79%) 61 (71%)
[0065] This embodiment indicates the SEC61β autoantibody has high capability to be a serological marker to detect the colorectal cancer; especially in the early stage, the SEC61β autoantibody has the detection efficiency more than 75%, which is helpful to promote the early detection and the prognosis evaluation.
Embodiment 3
The Capability of a STOML2 Protein as a Serological Marker for Detecting the Colorectal Cancer
[0066] A STOML2 protein is selected and listed in the Table 3 to be identified the capability to detect the colorectal cancer.
[0067] This embodiment has a difference with the embodiment 2, that is, this embodiment uses an ELISA method to detect the expression of the STOML2 protein in blood samples of colorectal cancer patients or healthy controls.
[0068] The STOML2 of the embodiment has an UniProt accession number Q9UJZ1 with sequence shows as following:
TABLE-US-00008 10 20 30 40 50 60 MLARAARGTG ALLLRGSLLA SGRAPRRASS GLPRNTVVLF VPQQEAWVVE RMGRFHRILE 70 80 90 100 110 120 PGLNILIPVL DRIRYVQSLK EIVINVPEQS AVTLDNVTLQ IDGVLYLRIM DPYKASYGVE 130 140 150 160 170 180 DPEYAVTQLA QTTMRSELGK LSLDKVFRER ESLNASIVDA INQAADCWGI RCLRYEIKDI 190 200 210 220 230 240 HVPPRVKESM QMQVEAERRK RATVLESEGT RESAINVAEG KKQAQILASE AEKAEQINQA 250 260 270 280 290 300 AGEASAVLAK AKAKAEAIRI LAAALTQHNG DAAASLTVAE QYVSAFSKLA KDSNTILLPS 310 320 330 340 350 NPGDVTSMVA QAMGVYGALT KAPVPGTPDS LSSGSSRDVQ GTDASLDEEL DRVKMS
[0069] However, one of ordinary skill in the art will realize that any sequence has more than 90% similarity with above-mentioned sequence is capable to apply in the present invention.
[0070] With reference to FIGS. 12 and 13, the expression of the STOML2 has significant difference in the blood samples of the colorectal cancer patient and the healthy control, which is similar to the results of the embodiment 1 and 2. Also, combination of the STOML2 protein and the current used CEA marker increases the detection capability of the STOML2 protein.
[0071] With reference to FIGS. 14 and 15, shows the detection efficiency and the specificity of the STOML 2 autoantibody in detecting the colorectal cancer. The STOML 2 autoantibody in the blood sample of the colorectal cancer is significantly higher than in the healthy control. The STOML 2 autoantibody level in the colorectal cancer is also higher than other cancers.
Embodiment 4
[0072] In this embodiment, the sensitivity and the specificity of different antigens is calculated by a backward elimination method with multivariate logistic regression model. All antigens have excellent specificity and are able to be applied alone or combined each other to improve the efficiency of the colorectal cancer detection.
TABLE-US-00009 TABLE 6 The sensitivity and the specificity of different antigens in detecting the colorectal cancer antigen sensitivity (%) specificity (%) AUC1 p value2 RPH3AL 13.83 90.67 0.554 0.33 RPL36 22.34 96 0.597 <0.05 STOML2 36.17 90.67 0.666 <0.001 P53 31.91 94.67 0.655 <0.001 Survivin 14.89 93.33 0.574 0.07 ANXA4 11.7 94.67 0.523 0.51 SEC61β 18.09 97.33 0.612 <0.001 STOML2 + P53 + Survivin + ANXA4 52.1 99 0.754 1AUC: area under ROC curve 2p-value is calculated by t-test
Sequence CWU
1
1
31318PRTHomo sapiensmisc_featurePLSCR1 1Met Asp Lys Gln Asn Ser Gln Met
Asn Ala Ser His Pro Glu Thr Asn1 5 10
15Leu Pro Val Gly Tyr Pro Pro Gln Tyr Pro Pro Thr Ala Phe
Gln Gly 20 25 30Pro Pro Gly
Tyr Ser Gly Tyr Pro Gly Pro Gln Val Ser Tyr Pro Pro 35
40 45Pro Pro Ala Gly His Ser Gly Pro Gly Pro Ala
Gly Phe Pro Val Pro 50 55 60Asn Gln
Pro Val Tyr Asn Gln Pro Val Tyr Asn Gln Pro Val Gly Ala65
70 75 80Ala Gly Val Pro Trp Met Pro
Ala Pro Gln Pro Pro Leu Asn Cys Pro 85 90
95Pro Gly Leu Glu Tyr Leu Ser Gln Ile Asp Gln Ile Leu
Ile His Gln 100 105 110Gln Ile
Glu Leu Leu Glu Val Leu Thr Gly Phe Glu Thr Asn Asn Lys 115
120 125Tyr Glu Ile Lys Asn Ser Phe Gly Gln Arg
Val Tyr Phe Ala Ala Glu 130 135 140Asp
Thr Asp Cys Cys Thr Arg Asn Cys Cys Gly Pro Ser Arg Pro Phe145
150 155 160Thr Leu Arg Ile Ile Asp
Asn Met Gly Gln Glu Val Ile Thr Leu Glu 165
170 175Arg Pro Leu Arg Cys Ser Ser Cys Cys Cys Pro Cys
Cys Leu Gln Glu 180 185 190Ile
Glu Ile Gln Ala Pro Pro Gly Val Pro Ile Gly Tyr Val Ile Gln 195
200 205Thr Trp His Pro Cys Leu Pro Lys Phe
Thr Ile Gln Asn Glu Lys Arg 210 215
220Glu Asp Val Leu Lys Ile Ser Gly Pro Cys Val Val Cys Ser Cys Cys225
230 235 240Gly Asp Val Asp
Phe Glu Ile Lys Ser Leu Asp Glu Gln Cys Val Val 245
250 255Gly Lys Ile Ser Lys His Trp Thr Gly Ile
Leu Arg Glu Ala Phe Thr 260 265
270Asp Ala Asp Asn Phe Gly Ile Gln Phe Pro Leu Asp Leu Asp Val Lys
275 280 285Met Lys Ala Val Met Ile Gly
Ala Cys Phe Leu Ile Asp Phe Met Phe 290 295
300Phe Glu Ser Thr Gly Ser Gln Glu Gln Lys Ser Gly Val Trp305
310 315296PRTHomo sapiensmisc_featureSEC61Beta
2Met Pro Gly Pro Thr Pro Ser Gly Thr Asn Val Gly Ser Ser Gly Arg1
5 10 15Ser Pro Ser Lys Ala Val
Ala Ala Arg Ala Ala Gly Ser Thr Val Arg 20 25
30Gln Arg Lys Asn Ala Ser Cys Gly Thr Arg Ser Ala Gly
Arg Thr Thr 35 40 45Ser Ala Gly
Thr Gly Gly Met Trp Arg Phe Tyr Thr Glu Asp Ser Pro 50
55 60Gly Leu Lys Val Gly Pro Val Pro Val Leu Val Met
Ser Leu Leu Phe65 70 75
80Ile Ala Ser Val Phe Met Leu His Ile Trp Gly Lys Tyr Thr Arg Ser
85 90 953356PRTHomo
sapiensmisc_featureSTOML2 3Met Leu Ala Arg Ala Ala Arg Gly Thr Gly Ala
Leu Leu Leu Arg Gly1 5 10
15Ser Leu Leu Ala Ser Gly Arg Ala Pro Arg Arg Ala Ser Ser Gly Leu
20 25 30Pro Arg Asn Thr Val Val Leu
Phe Val Pro Gln Gln Glu Ala Trp Val 35 40
45Val Glu Arg Met Gly Arg Phe His Arg Ile Leu Glu Pro Gly Leu
Asn 50 55 60Ile Leu Ile Pro Val Leu
Asp Arg Ile Arg Tyr Val Gln Ser Leu Lys65 70
75 80Glu Ile Val Ile Asn Val Pro Glu Gln Ser Ala
Val Thr Leu Asp Asn 85 90
95Val Thr Leu Gln Ile Asp Gly Val Leu Tyr Leu Arg Ile Met Asp Pro
100 105 110Tyr Lys Ala Ser Tyr Gly
Val Glu Asp Pro Glu Tyr Ala Val Thr Gln 115 120
125Leu Ala Gln Thr Thr Met Arg Ser Glu Leu Gly Lys Leu Ser
Leu Asp 130 135 140Lys Val Phe Arg Glu
Arg Glu Ser Leu Asn Ala Ser Ile Val Asp Ala145 150
155 160Ile Asn Gln Ala Ala Asp Cys Trp Gly Ile
Arg Cys Leu Arg Tyr Glu 165 170
175Ile Lys Asp Ile His Val Pro Pro Arg Val Lys Glu Ser Met Gln Met
180 185 190Gln Val Glu Ala Glu
Arg Arg Lys Arg Ala Thr Val Leu Glu Ser Glu 195
200 205Gly Thr Arg Glu Ser Ala Ile Asn Val Ala Glu Gly
Lys Lys Gln Ala 210 215 220Gln Ile Leu
Ala Ser Glu Ala Glu Lys Ala Glu Gln Ile Asn Gln Ala225
230 235 240Ala Gly Glu Ala Ser Ala Val
Leu Ala Lys Ala Lys Ala Lys Ala Glu 245
250 255Ala Ile Arg Ile Leu Ala Ala Ala Leu Thr Gln His
Asn Gly Asp Ala 260 265 270Ala
Ala Ser Leu Thr Val Ala Glu Gln Tyr Val Ser Ala Phe Ser Lys 275
280 285Leu Ala Lys Asp Ser Asn Thr Ile Leu
Leu Pro Ser Asn Pro Gly Asp 290 295
300Val Thr Ser Met Val Ala Gln Ala Met Gly Val Tyr Gly Ala Leu Thr305
310 315 320Lys Ala Pro Val
Pro Gly Thr Pro Asp Ser Leu Ser Ser Gly Ser Ser 325
330 335Arg Asp Val Gln Gly Thr Asp Ala Ser Leu
Asp Glu Glu Leu Asp Arg 340 345
350Val Lys Met Ser 355
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