Stromal cells do not share KRAS mutations that the epithelial component harbors in colorectal carcinomas

被引:3
作者
Baloglu, Huseyin [1 ]
Yigit, Nuri [1 ]
机构
[1] GATA Haydarpasa Training Hosp, Dept Pathol, TR-34668 Istanbul, Turkey
关键词
Colorectal cancer; Cancer stroma; KRAS; TUMOR-STROMA; CANCER STROMA; MICROENVIRONMENT; FIBROBLASTS; INSTABILITY;
D O I
10.1016/j.canlet.2011.04.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epithelia and stroma are the main components of carcinomas that have impact on carcinogenesis. Many of the genetic changes harboring in the epithelia may possibly be seen in stromal cells during neoplastic transformation. We intended to investigate weather KRAS mutations are shared by the stromal cells in colorectal adenocarcinomas. Forty cases with KRAS mutation were studied. Glandular/epithelial and the stromal components of each primary tumor were collected and KRAS mutation analysis was performed. None of the cases revealed KRAS mutations in stromal integral. We concluded that stromal cells in colorectal carcinoma do not share KRAS mutations that the epithelial component harbors. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:118 / 121
页数:4
相关论文
共 17 条
[1]   Targeting the Tumor Stroma in Cancer Therapy [J].
Anton, Kevin ;
Glod, John .
CURRENT PHARMACEUTICAL BIOTECHNOLOGY, 2009, 10 (02) :185-191
[2]   Combined total genome loss of heterozygosity scan of breast cancer stroma and epithelium reveals multiplicity of stromal targets [J].
Fukino, K ;
Lei, S ;
Matsumoto, S ;
Morrison, CD ;
Mutter, GL ;
Eng, C .
CANCER RESEARCH, 2004, 64 (20) :7231-7236
[3]   Clinical relevance of EGFR- and KRAS-status in colorectal cancer patients treated with monoclonal antibodies directed against the EGFR [J].
Heinemann, Volker ;
Stintzing, Sebastian ;
Kirchner, Thomas ;
Boeck, Stefan ;
Jung, Andreas .
CANCER TREATMENT REVIEWS, 2009, 35 (03) :262-271
[4]   Epithelial and stromal genetic instability contributes to genesis of colorectal adenomas [J].
Ishiguro, K ;
Yoshida, T ;
Yagishita, H ;
Numata, Y ;
Okayasu, T .
GUT, 2006, 55 (05) :695-702
[5]   Cellular and molecular phenotypes of proliferating stromal cells from human carcinomas [J].
Kopantzev, E. P. ;
Vayshlya, N. A. ;
Kopantseva, M. R. ;
Egorov, V. I. ;
Pikunov, M. ;
Zinovyeva, M. V. ;
Vinogradova, T. V. ;
Zborovskaya, I. B. ;
Sverdlov, E. D. .
BRITISH JOURNAL OF CANCER, 2010, 102 (10) :1533-1540
[6]   Genetic model of multi-step breast carcinogenesis involving the epithelium and stroma: clues to tumour-microenvironment interactions [J].
Kurose, K ;
Hoshaw-Woodard, S ;
Adeyinka, A ;
Lemeshow, S ;
Watson, PH ;
Eng, C .
HUMAN MOLECULAR GENETICS, 2001, 10 (18) :1907-1913
[7]   Frequent somatic mutations in PTEN and TP53 are mutually exclusive in the stroma of breast carcinomas [J].
Kurose, K ;
Gilley, K ;
Matsumoto, S ;
Watson, PH ;
Zhou, XP ;
Eng, C .
NATURE GENETICS, 2002, 32 (03) :355-357
[8]   Cancer-Associated Fibroblasts Enhance the Gland-Forming Capability of Prostate Cancer Stem Cells [J].
Liao, Chun-Peng ;
Adisetiyo, Helty ;
Liang, Mengmeng ;
Roy-Burman, Pradip .
CANCER RESEARCH, 2010, 70 (18) :7294-7303
[9]   Importance of Wnt Signaling in the Tumor Stroma Microenvironment [J].
Macheda, Maria L. ;
Stacker, Steven A. .
CURRENT CANCER DRUG TARGETS, 2008, 8 (06) :454-465
[10]   Tumor-stroma interactions in pancreatic ductal adenocarcinoma [J].
Mahadevan, Daruka ;
Von Hoff, Daniel D. .
MOLECULAR CANCER THERAPEUTICS, 2007, 6 (04) :1186-1197