Lack of mutation at codon 531 of SRC in advanced colorectal cancers from Italian patients

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Abstract

A truncating mutation (C to T transition) at codon 531 of the human protooncogene c-src, possibly accounting for the activation of c-src tyrosine kinase, has been recently identified in a subset of advanced colorectal cancer from North-American patients. However, two subsequent studies have failed to confirm the occurrence of SRC 531 mutation in colorectal cancers from North-European and Asiatic patients, raising the hypothesis that the genetic activation of src in colon cancer might be restricted to patients belonging to specific ethnic groups. We investigated a large series of colorectal cancers from Italian patients (155 cases) with a high prevalence of liver metastasis (43%). Using a PCR-RFLP assay, the occurrence of a SRC 531 mutation was ruled out in all the investigated specimens of primary tumours and/or metastases. Our results demonstrate that SRC Gln531AMB plays no role in the development or in the progression of colorectal cancer among Italian patients. © 2001 Cancer Research Campaign.

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Laghi, L., Bianchi, P., Orbetegli, O., Gennari, L., Roncalli, M., & Malesci, A. (2001). Lack of mutation at codon 531 of SRC in advanced colorectal cancers from Italian patients. British Journal of Cancer, 84(2), 196–198. https://doi.org/10.1054/bjoc.2000.1560

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