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SMAD7 is a prognostic marker in patients with colorectal cancer
Author(s) -
Boulay JeanLouis,
Mild Gabriele,
Lowy Adam,
Reuter Juergen,
Lagrange Magali,
Terracciano Luigi,
Laffer Urban,
Herrmann Richard,
Rochlitz Christoph
Publication year - 2003
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.10908
Subject(s) - colorectal cancer , medicine , cancer research , hazard ratio , smad , gene duplication , oncology , clinical significance , predictive marker , transforming growth factor , biology , gene , cancer , confidence interval , genetics
Chromosomal region 18q21 is frequently deleted in colorectal cancer (CRC) and is associated with poor prognosis. Potential tumor suppressor mechanisms altered by 18q21 deletion include mediation of TGFβ signaling by SMADs. Following the definition of SMAD4 deletion as a negative predictive marker for chemotherapy benefit in patients with CRC, we aimed to evaluate the clinical relevance of the deletion of other SMAD genes clustered in this region: SMAD2 and SMAD7 in 264 CRC biopsies from a previous clinical study. In contrast to SMAD2 deletion, for which no clinical relevance was observed, hazard ratios (HR) in a multivariate analysis associated with SMAD7 deletion [overall survival (OS): HR = 0.43, p = 0.0012; disease‐free survival (DFS): HR = 0.50, p = 0.0033] indicated a favorable outcome for these patients. In addition, SMAD7 duplication had a hazardous effect on survival [OS: HR = 2.10, p = 0.020; DFS: HR = 2.06, p = 0.015]. Moreover, the HRs associated with one additional copy of SMAD7 were 1.76, p = 0.00024 [OS] and 1.64, p = 0.00048 [DFS] respectively, showing a graded effect of SMAD7 on patient outcome depending on gene copy number that suggests a dose‐and‐effect basis. Since SMAD7 blocks TGFβ signaling, these data are consistent with the loss of SMAD7 rendering carcinoma cells more sensitive to cell growth arrest/apoptotic effect of TGFβ, whereas gain of SMAD7 function might result in TGFβ resistance, thereby emphasizing the role of TGFβ in tumor suppression. © 2003 Wiley‐Liss, Inc.