| Literature DB >> 18755584 |
Virginie Granci1, Frédéric Bibeau, Andrew Kramar, Florence Boissière-Michot, Simon Thézénas, Agnès Thirion, Céline Gongora, Pierre Martineau, Maguy Del Rio, Marc Ychou.
Abstract
Drug resistance is believed to cause treatment failure in patients with metastatic colorectal carcinoma (CRC). Resistance to chemotherapy can involve different processes, including apoptosis, whose extrinsic pathway is regulated by expression of death-inducing TRAIL-R1 and -R2 and inhibitory TRAIL-R3 and -R4 cell surface receptors. Therefore, we investigated whether variations in their expression could influence the response to 5-Fluorouracil (5-FU) in metastatic CRC. We analysed TRAIL-R 1, -2, -3 and -4 expression by immuno-histochemistry in CRC, using tissue micro arrays, and found that concomitant low/medium TRAIL-R1 and high TRAIL-R3 expression in primary CRC is significantly associated with a poor response to 5-FU-based first-line chemotherapy and with shorter progression-free survival. Specifically, the median progression-free survival was 3.1 months (poor prognostic group) versus 10.1 in the good prognostic group. Thus, the combination of TRAIL-R1 and TRAIL-R3 expression might represent a predictive and prognostic factor of the response to 5-FU-based first-line chemotherapy in patients with metastatic CRC.Entities:
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Year: 2008 PMID： 18755584 DOI： 10.1016/j.ejca.2008.06.042
Source DB: PubMed Journal: Eur J Cancer ISSN： 0959-8049 Impact factor: 9.162