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SNPs in the coding region of the metastasis-inducing gene MACC1 and clinical outcome in colorectal cancer

BACKGROUND: Colorectal cancer is one of the main cancers in the Western world. About 90% of the deaths arise from formation of distant metastasis. The expression of the newly identified gene metastasis associated in colon cancer 1 (MACC1) is a prognostic indicator for colon cancer metastasis. Here,...

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Autores principales: Schmid, Felicitas, Burock, Susen, Klockmeier, Konrad, Schlag, Peter M, Stein, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3480947/
https://www.ncbi.nlm.nih.gov/pubmed/22838389
http://dx.doi.org/10.1186/1476-4598-11-49
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author Schmid, Felicitas
Burock, Susen
Klockmeier, Konrad
Schlag, Peter M
Stein, Ulrike
author_facet Schmid, Felicitas
Burock, Susen
Klockmeier, Konrad
Schlag, Peter M
Stein, Ulrike
author_sort Schmid, Felicitas
collection PubMed
description BACKGROUND: Colorectal cancer is one of the main cancers in the Western world. About 90% of the deaths arise from formation of distant metastasis. The expression of the newly identified gene metastasis associated in colon cancer 1 (MACC1) is a prognostic indicator for colon cancer metastasis. Here, we analyzed for the first time the impact of single nucleotide polymorphisms (SNPs) in the coding region of MACC1 for clinical outcome of colorectal cancer patients. Additionally, we screened met proto-oncogene (Met), the transcriptional target gene of MACC1, for mutations. METHODS: We sequenced the coding exons of MACC1 in 154 colorectal tumors (stages I, II and III) and the crucial exons of Met in 60 colorectal tumors (stages I, II and III). We analyzed the association of MACC1 polymorphisms with clinical data, including metachronous metastasis, UICC stages, tumor invasion, lymph node metastasis and patients’ survival (n = 154, stages I, II and III). Furthermore, we performed biological assays in order to evaluate the functional impact of MACC1 SNPs on the motility of colorectal cancer cells. RESULTS: We genotyped three MACC1 SNPs in the coding region. Thirteen % of the tumors had the genotype cg (rs4721888, L31V), 48% a ct genotype (rs975263, S515L) and 84% a gc or cc genotype (rs3735615, R804T). We found no association of these SNPs with clinicopathological parameters or with patients’ survival, when analyzing the entire patients’ cohort. An increased risk for a shorter metastasis-free survival of patients with a ct genotype (rs975263) was observed in younger colon cancer patients with stage I or II (P = 0.041, n = 18). In cell culture, MACC1 SNPs did not affect MACC1-induced cell motility and proliferation. CONCLUSION: In summary, the identification of coding MACC1 SNPs in primary colorectal tumors does not improve the prediction for metastasis formation or for patients’ survival compared to MACC1 expression analysis alone. The ct genotype (rs975263) might be associated with a reduced survival for younger colon cancer patients in early stages. However, further studies with larger sample sizes are needed.
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spelling pubmed-34809472012-10-27 SNPs in the coding region of the metastasis-inducing gene MACC1 and clinical outcome in colorectal cancer Schmid, Felicitas Burock, Susen Klockmeier, Konrad Schlag, Peter M Stein, Ulrike Mol Cancer Research BACKGROUND: Colorectal cancer is one of the main cancers in the Western world. About 90% of the deaths arise from formation of distant metastasis. The expression of the newly identified gene metastasis associated in colon cancer 1 (MACC1) is a prognostic indicator for colon cancer metastasis. Here, we analyzed for the first time the impact of single nucleotide polymorphisms (SNPs) in the coding region of MACC1 for clinical outcome of colorectal cancer patients. Additionally, we screened met proto-oncogene (Met), the transcriptional target gene of MACC1, for mutations. METHODS: We sequenced the coding exons of MACC1 in 154 colorectal tumors (stages I, II and III) and the crucial exons of Met in 60 colorectal tumors (stages I, II and III). We analyzed the association of MACC1 polymorphisms with clinical data, including metachronous metastasis, UICC stages, tumor invasion, lymph node metastasis and patients’ survival (n = 154, stages I, II and III). Furthermore, we performed biological assays in order to evaluate the functional impact of MACC1 SNPs on the motility of colorectal cancer cells. RESULTS: We genotyped three MACC1 SNPs in the coding region. Thirteen % of the tumors had the genotype cg (rs4721888, L31V), 48% a ct genotype (rs975263, S515L) and 84% a gc or cc genotype (rs3735615, R804T). We found no association of these SNPs with clinicopathological parameters or with patients’ survival, when analyzing the entire patients’ cohort. An increased risk for a shorter metastasis-free survival of patients with a ct genotype (rs975263) was observed in younger colon cancer patients with stage I or II (P = 0.041, n = 18). In cell culture, MACC1 SNPs did not affect MACC1-induced cell motility and proliferation. CONCLUSION: In summary, the identification of coding MACC1 SNPs in primary colorectal tumors does not improve the prediction for metastasis formation or for patients’ survival compared to MACC1 expression analysis alone. The ct genotype (rs975263) might be associated with a reduced survival for younger colon cancer patients in early stages. However, further studies with larger sample sizes are needed. BioMed Central 2012-07-29 /pmc/articles/PMC3480947/ /pubmed/22838389 http://dx.doi.org/10.1186/1476-4598-11-49 Text en Copyright ©2012 Schmid et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Schmid, Felicitas
Burock, Susen
Klockmeier, Konrad
Schlag, Peter M
Stein, Ulrike
SNPs in the coding region of the metastasis-inducing gene MACC1 and clinical outcome in colorectal cancer
title SNPs in the coding region of the metastasis-inducing gene MACC1 and clinical outcome in colorectal cancer
title_full SNPs in the coding region of the metastasis-inducing gene MACC1 and clinical outcome in colorectal cancer
title_fullStr SNPs in the coding region of the metastasis-inducing gene MACC1 and clinical outcome in colorectal cancer
title_full_unstemmed SNPs in the coding region of the metastasis-inducing gene MACC1 and clinical outcome in colorectal cancer
title_short SNPs in the coding region of the metastasis-inducing gene MACC1 and clinical outcome in colorectal cancer
title_sort snps in the coding region of the metastasis-inducing gene macc1 and clinical outcome in colorectal cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3480947/
https://www.ncbi.nlm.nih.gov/pubmed/22838389
http://dx.doi.org/10.1186/1476-4598-11-49
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