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Impact of primary colorectal Cancer location on the KRAS status and its prognostic value
BACKGROUND: Colorectal cancer (CRC) originating from the right-sided or left-sided colon is distinct clinicopathological entity. The KRAS status and its prognostic value in CRC remain controversial. This study aimed to investigate the association of KRAS status with clinicopathological features and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437985/ https://www.ncbi.nlm.nih.gov/pubmed/30917791 http://dx.doi.org/10.1186/s12876-019-0965-5 |
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author | Xie, Ming-zhi Li, Ji-lin Cai, Zheng-min Li, Ke-zhi Hu, Bang-li |
author_facet | Xie, Ming-zhi Li, Ji-lin Cai, Zheng-min Li, Ke-zhi Hu, Bang-li |
author_sort | Xie, Ming-zhi |
collection | PubMed |
description | BACKGROUND: Colorectal cancer (CRC) originating from the right-sided or left-sided colon is distinct clinicopathological entity. The KRAS status and its prognostic value in CRC remain controversial. This study aimed to investigate the association of KRAS status with clinicopathological features and prognostic value in CRC. METHODS: 178 colon cancer and 145 rectal cancer patients were enrolled. KRAS mutation test was performed on paraffin-embedded tumor samples using PCR methods. The colon cancer was divided into right-sided colon cancer (RCC) and left-sided colon cancer (LCC). Studies that reported the association of KRAS mutation with CRC clinical features and prognosis in databases were searched prior to 2018. The data of the present study was combined with the data of published studies using meta-analysis methods. RESULTS: No significant difference between colon cancer and rectal cancer regarding the KRAS status. The KRAS mutation was much frequent in RCC than in LCC (p = 0.010). 17 studies with 11,385 colon cancer patients were selected, the pooled results of our data and previous published data showed that KRAS mutation was more frequent in RCC compared with in LCC (p < 0.01); KRAS mutation was not associated with the prognosis in RCC patient; however, KRAS mutation indicated a poor prognosis in LCC patients compared with KRAS wild type (p < 0.01). CONCLUSION: KRAS status has no difference between colon cancer and rectal cancer. KRAS mutation was more frequent in RCC than in LCC, and associated with a poor prognosis in LCC patients, but not in RCC patients. |
format | Online Article Text |
id | pubmed-6437985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64379852019-04-08 Impact of primary colorectal Cancer location on the KRAS status and its prognostic value Xie, Ming-zhi Li, Ji-lin Cai, Zheng-min Li, Ke-zhi Hu, Bang-li BMC Gastroenterol Research Article BACKGROUND: Colorectal cancer (CRC) originating from the right-sided or left-sided colon is distinct clinicopathological entity. The KRAS status and its prognostic value in CRC remain controversial. This study aimed to investigate the association of KRAS status with clinicopathological features and prognostic value in CRC. METHODS: 178 colon cancer and 145 rectal cancer patients were enrolled. KRAS mutation test was performed on paraffin-embedded tumor samples using PCR methods. The colon cancer was divided into right-sided colon cancer (RCC) and left-sided colon cancer (LCC). Studies that reported the association of KRAS mutation with CRC clinical features and prognosis in databases were searched prior to 2018. The data of the present study was combined with the data of published studies using meta-analysis methods. RESULTS: No significant difference between colon cancer and rectal cancer regarding the KRAS status. The KRAS mutation was much frequent in RCC than in LCC (p = 0.010). 17 studies with 11,385 colon cancer patients were selected, the pooled results of our data and previous published data showed that KRAS mutation was more frequent in RCC compared with in LCC (p < 0.01); KRAS mutation was not associated with the prognosis in RCC patient; however, KRAS mutation indicated a poor prognosis in LCC patients compared with KRAS wild type (p < 0.01). CONCLUSION: KRAS status has no difference between colon cancer and rectal cancer. KRAS mutation was more frequent in RCC than in LCC, and associated with a poor prognosis in LCC patients, but not in RCC patients. BioMed Central 2019-03-27 /pmc/articles/PMC6437985/ /pubmed/30917791 http://dx.doi.org/10.1186/s12876-019-0965-5 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Xie, Ming-zhi Li, Ji-lin Cai, Zheng-min Li, Ke-zhi Hu, Bang-li Impact of primary colorectal Cancer location on the KRAS status and its prognostic value |
title | Impact of primary colorectal Cancer location on the KRAS status and its prognostic value |
title_full | Impact of primary colorectal Cancer location on the KRAS status and its prognostic value |
title_fullStr | Impact of primary colorectal Cancer location on the KRAS status and its prognostic value |
title_full_unstemmed | Impact of primary colorectal Cancer location on the KRAS status and its prognostic value |
title_short | Impact of primary colorectal Cancer location on the KRAS status and its prognostic value |
title_sort | impact of primary colorectal cancer location on the kras status and its prognostic value |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437985/ https://www.ncbi.nlm.nih.gov/pubmed/30917791 http://dx.doi.org/10.1186/s12876-019-0965-5 |
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