B7-H3 expression in colorectal cancer: associations with clinicopathological parameters and patient outcome

被引:80
作者
Ingebrigtsen, Vibeke A. [1 ,2 ]
Boye, Kjetil [1 ,3 ]
Nesland, Jahn M. [2 ,4 ]
Nesbakken, Arild [2 ,6 ]
Flatmark, Kjersti [1 ,5 ]
Fodstad, Oystein [1 ,2 ]
机构
[1] Oslo Univ Hosp, Norwegian Radium Hosp, Dept Tumor Biol, N-0424 Oslo, Norway
[2] Univ Oslo, Fac Med, Inst Clin Med, N-0318 Oslo, Norway
[3] Oslo Univ Hosp, Norwegian Radium Hosp, Dept Oncol, N-0424 Oslo, Norway
[4] Oslo Univ Hosp, Norwegian Radium Hosp, Dept Pathol, N-0424 Oslo, Norway
[5] Oslo Univ Hosp, Norwegian Radium Hosp, Dept Surg Gastroenterol, N-0424 Oslo, Norway
[6] Oslo Univ Hosp, Dept Gastrointestinal Surg, N-0424 Oslo, Norway
关键词
Colorectal cancer; Nuclear B7-H3; Prognostic biomarker; Tissue microarray; COSTIMULATORY MOLECULE B7-H3; MICROSATELLITE INSTABILITY; COLON-CANCER; LIGAND EXPRESSION; PROSTATE-CANCER; TUMOR-CELL; STAGE-II; SURVIVAL; SENSITIVITY; PROGNOSIS;
D O I
10.1186/1471-2407-14-602
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: We have previously reported overexpression of the immunoregulatory protein B7-H3 in colorectal cancer and that nuclear expression predicted poor outcome in colon cancer patients. The present study was performed to examine the prognostic role of B7-H3 in an independent colorectal cancer cohort. Methods: Using tissue microarrays from 731 colorectal cancer patients, tumour B7-H3 expression was assessed by immunohistochemistry. Associations with clinicopathological parameters and patient outcome were investigated. Results: Nuclear expression of B7-H3 in cancer cells was present in 27% of the samples in the total study cohort, while cytoplasmic/membrane and stromal expression was seen in 86% and 77% of the samples, respectively. Nuclear B7-H3 had no prognostic relevance in the complete outcome cohort, neither in colon cancer patients. However, nuclear B7-H3 was significantly associated with reduced recurrence-free survival in TNM stage I colorectal cancer patients. Conclusions: Overexpression of B7-H3 in colorectal cancer was confirmed, but in contrast to previous results, nuclear B7-H3 was not a strong prognostic biomarker in this cohort. The discrepancy might be related to the use of single-core tissue microarrays for detection of the heterogeneously expressed B7-H3, and the role of B7-H3 in colorectal cancer still needs further examination.
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页数:9
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