Expression Profiling of Stem Cell-Related Genes in Neoadjuvant-Treated Gastric Cancer: A NOTCH2, GSK3B and β-catenin Gene Signature Predicts Survival

被引:32
作者
Bauer, Lukas [1 ]
Langer, Rupert [1 ]
Becker, Karen [1 ]
Hapfelmeier, Alexander [4 ]
Ott, Katja [2 ]
Novotny, Alexander [3 ]
Hoefler, Heinz [1 ,5 ]
Keller, Gisela [1 ]
机构
[1] Tech Univ Munich, Inst Pathol, Munich, Germany
[2] Heidelberg Univ, Dept Surg, D-6900 Heidelberg, Germany
[3] Tech Univ Munich, Dept Surg, Munich, Germany
[4] Tech Univ Munich, Inst Med Stat & Epidemiol, Munich, Germany
[5] Helmholtz Zentrum Munchen, Inst Pathol, Neuherberg, Germany
关键词
BREAST-CANCER; SELF-RENEWAL; MARKERS; CHEMOTHERAPY; CARCINOMAS; REGRESSION; PATTERNS; TUMOR; PHOSPHORYLATION; CARCINOGENESIS;
D O I
10.1371/journal.pone.0044566
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cancer stem cell (CSC) based gene expression signatures are associated with prognosis in various tumour types and CSCs are suggested to be particularly drug resistant. The aim of our study was first, to determine the prognostic significance of CSC-related gene expression in residual tumour cells of neoadjuvant-treated gastric cancer (GC) patients. Second, we wished to examine, whether expression alterations between pre- and post-therapeutic tumour samples exist, consistent with an enrichment of drug resistant tumour cells. The expression of 44 genes was analysed in 63 formalin-fixed, paraffin embedded tumour specimens with partial tumour regression (10-50% residual tumour) after neoadjuvant chemotherapy by quantitative real time PCR low-density arrays. A signature of combined GSK3B(high), beta-catenin (CTNNB1)(high) and NOTCH2(low) expression was strongly correlated with better patient survival (p < 0.001). A prognostic relevance of these genes was also found analysing publically available gene expression data. The expression of 9 genes was compared between pretherapeutic biopsies and post-therapeutic resected specimens. A significant post-therapeutic increase in NOTCH2, LGR5 and POU5F1 expression was found in tumours with different tumour regression grades. No significant alterations were observed for GSK3B and CTNNB1. Immunohistochemical analysis demonstrated a chemotherapy-associated increase in the intensity of NOTCH2 staining, but not in the percentage of NOTCH2. Taken together, the GSK3B, CTNNB1 and NOTCH2 expression signature is a novel, promising prognostic parameter for GC. The results of the differential expression analysis indicate a prominent role for NOTCH2 and chemotherapy resistance in GC, which seems to be related to an effect of the drugs on NOTCH2 expression rather than to an enrichment of NOTCH2 expressing tumour cells.
引用
收藏
页数:9
相关论文
共 52 条
[1]   Lgr5+ve Stem Cells Drive Self-Renewal in the Stomach and Build Long-Lived Gastric Units In Vitro [J].
Barker, Nick ;
Huch, Meritxell ;
Kujala, Pekka ;
van de Wetering, Marc ;
Snippert, Hugo J. ;
van Es, Johan H. ;
Sato, Toshiro ;
Stange, Daniel E. ;
Begthel, Harry ;
van den Born, Maaike ;
Danenberg, Esther ;
van den Brink, Stieneke ;
Korving, Jeroen ;
Abo, Arie ;
Peters, Peter J. ;
Wright, Nick ;
Poulsom, Richard ;
Clevers, Hans .
CELL STEM CELL, 2010, 6 (01) :25-36
[2]   Significance of Histopathological Tumor Regression After Neoadjuvant Chemotherapy in Gastric Adenocarcinomas A Summary of 480 Cases [J].
Becker, Karen ;
Langer, Rupert ;
Reim, Daniel ;
Novotny, Alexander ;
zum Buschenfelde, Christian Meyer ;
Engel, Jutta ;
Friess, Helmut ;
Hofler, Heinz .
ANNALS OF SURGERY, 2011, 253 (05) :934-939
[3]   An embryonic stem cell-like gene expression signature in poorly differentiated aggressive human tumors [J].
Ben-Porath, Ittai ;
Thomson, Matthew W. ;
Carey, Vincent J. ;
Ge, Ruping ;
Bell, George W. ;
Regev, Aviv ;
Weinberg, Robert A. .
NATURE GENETICS, 2008, 40 (05) :499-507
[4]  
Chen X, 2003, MOL BIOL CELL, V14, P3208, DOI 10.1091/mbc.E02-12-0833
[5]   Gene Expression Signature-Based Prognostic Risk Score in Gastric Cancer [J].
Cho, Jae Yong ;
Lim, Jae Yun ;
Cheong, Jae Ho ;
Park, Yun-Yong ;
Yoon, Se-Lyun ;
Kim, Soo Mi ;
Kim, Sang-Bae ;
Kim, Hoguen ;
Hong, Soon Won ;
Park, Young Nyun ;
Noh, Sung Hoon ;
Park, Eun Sung ;
Chu, In-Sun ;
Hong, Waun Ki ;
Ajani, Jaffer A. ;
Lee, Ju-Seog .
CLINICAL CANCER RESEARCH, 2011, 17 (07) :1850-1857
[6]   The cancer stem cell: premises, promises and challenges [J].
Clevers, Hans .
NATURE MEDICINE, 2011, 17 (03) :313-319
[7]   Open source clustering software [J].
de Hoon, MJL ;
Imoto, S ;
Nolan, J ;
Miyano, S .
BIOINFORMATICS, 2004, 20 (09) :1453-1454
[8]   Methylation of Cancer-Stem-Cell-Associated Wnt Target Genes Predicts Poor Prognosis in Colorectal Cancer Patients [J].
de Sousa e Melo, Felipe ;
Colak, Selcuk ;
Buikhuisen, Joyce ;
Koster, Jan ;
Cameron, Kate ;
de Jong, Joan H. ;
Tuynman, Jurriaan B. ;
Prasetyanti, Pramudita R. ;
Fessler, Evelyn ;
van den Bergh, Saskia P. ;
Rodermond, Hans ;
Dekker, Evelien ;
van der Loos, Chris M. ;
Pals, Steven T. ;
van de Vijver, Marc J. ;
Versteeg, Rogier ;
Richel, Dick J. ;
Vermeulen, Louis ;
Medema, Jan Paul .
CELL STEM CELL, 2011, 9 (05) :476-485
[9]   Gene expression analysis identifies two groups of ovarian high-grade serous carcinomas with different prognosis [J].
Espinosa, Inigo ;
Catasus, Lluis ;
Canet, Belen ;
D'Angelo, Emanuela ;
Munoz, Josefina ;
Prat, Jaime .
MODERN PATHOLOGY, 2011, 24 (06) :846-854
[10]   Phosphorylation by glycogen synthase kinase-3β down-regulates Notch activity, a link for Notch and Wnt pathways [J].
Espinosa, L ;
Inglés-Esteve, J ;
Aguilera, C ;
Bigas, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (34) :32227-32235