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Prognostic value of microRNA-126 and CRK expression in gastric cancer

BACKGROUND: MicroRNA (miR)-126, acting as a tumor suppressor, has been reported to inhibit the invasion of gastric cancer cells in part by targeting v-crk sarcoma virus CT10 oncogene homologue (CRK). The aim of this study was to investigate the clinical significance of miR-126/CRK axis in gastric ca...

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Autores principales: Yue, Shun, Shi, Huichang, Han, Jun, Zhang, Tiecheng, Zhu, Weiguo, Zhang, Dahong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066993/
https://www.ncbi.nlm.nih.gov/pubmed/27785060
http://dx.doi.org/10.2147/OTT.S87778
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author Yue, Shun
Shi, Huichang
Han, Jun
Zhang, Tiecheng
Zhu, Weiguo
Zhang, Dahong
author_facet Yue, Shun
Shi, Huichang
Han, Jun
Zhang, Tiecheng
Zhu, Weiguo
Zhang, Dahong
author_sort Yue, Shun
collection PubMed
description BACKGROUND: MicroRNA (miR)-126, acting as a tumor suppressor, has been reported to inhibit the invasion of gastric cancer cells in part by targeting v-crk sarcoma virus CT10 oncogene homologue (CRK). The aim of this study was to investigate the clinical significance of miR-126/CRK axis in gastric cancer. METHODS: miR-126 and CRK mRNA expression levels were detected by real-time quantitative reverse transcription polymerase chain reaction in 220 self-pairs of gastric cancer and adjacent noncancerous tissues. RESULTS: Expression levels of miR-126 and CRK mRNA in gastric cancer tissues were, respectively, lower and higher than those in adjacent noncancerous tissues (both P<0.001). Low miR-126 expression and high CRK expression, alone or in combination, were all significantly associated with positive lymph node and distant metastases and advanced TNM stage of human gastric cancer (all P<0.05). We also found that the overall survival rates of the patients with low miR-126 expression and high CRK expression were, respectively, shorter than those with high miR-126 expression and low CRK expression. Interestingly, miR-126-low/CRK-high expression was associated with a significantly worse overall survival of all miR-126/CRK groups (P<0.001). Moreover, multivariate analysis identified miR-126 and/or CRK expression as independent prognostic factors for patients with gastric cancer. Notably, the prognostic relevance of miR-126 and/or CRK expression was more obvious in the subgroup of patients with TNM stage IV. CONCLUSION: Dysregulation of miR-126/CRK axis may promote the malignant progression of human gastric cancer. miR-126 and CRK combined expression may serve as an independent predictor of overall survival in patients with advanced gastric cancer.
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spelling pubmed-50669932016-10-26 Prognostic value of microRNA-126 and CRK expression in gastric cancer Yue, Shun Shi, Huichang Han, Jun Zhang, Tiecheng Zhu, Weiguo Zhang, Dahong Onco Targets Ther Original Research BACKGROUND: MicroRNA (miR)-126, acting as a tumor suppressor, has been reported to inhibit the invasion of gastric cancer cells in part by targeting v-crk sarcoma virus CT10 oncogene homologue (CRK). The aim of this study was to investigate the clinical significance of miR-126/CRK axis in gastric cancer. METHODS: miR-126 and CRK mRNA expression levels were detected by real-time quantitative reverse transcription polymerase chain reaction in 220 self-pairs of gastric cancer and adjacent noncancerous tissues. RESULTS: Expression levels of miR-126 and CRK mRNA in gastric cancer tissues were, respectively, lower and higher than those in adjacent noncancerous tissues (both P<0.001). Low miR-126 expression and high CRK expression, alone or in combination, were all significantly associated with positive lymph node and distant metastases and advanced TNM stage of human gastric cancer (all P<0.05). We also found that the overall survival rates of the patients with low miR-126 expression and high CRK expression were, respectively, shorter than those with high miR-126 expression and low CRK expression. Interestingly, miR-126-low/CRK-high expression was associated with a significantly worse overall survival of all miR-126/CRK groups (P<0.001). Moreover, multivariate analysis identified miR-126 and/or CRK expression as independent prognostic factors for patients with gastric cancer. Notably, the prognostic relevance of miR-126 and/or CRK expression was more obvious in the subgroup of patients with TNM stage IV. CONCLUSION: Dysregulation of miR-126/CRK axis may promote the malignant progression of human gastric cancer. miR-126 and CRK combined expression may serve as an independent predictor of overall survival in patients with advanced gastric cancer. Dove Medical Press 2016-10-11 /pmc/articles/PMC5066993/ /pubmed/27785060 http://dx.doi.org/10.2147/OTT.S87778 Text en © 2016 Yue et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Yue, Shun
Shi, Huichang
Han, Jun
Zhang, Tiecheng
Zhu, Weiguo
Zhang, Dahong
Prognostic value of microRNA-126 and CRK expression in gastric cancer
title Prognostic value of microRNA-126 and CRK expression in gastric cancer
title_full Prognostic value of microRNA-126 and CRK expression in gastric cancer
title_fullStr Prognostic value of microRNA-126 and CRK expression in gastric cancer
title_full_unstemmed Prognostic value of microRNA-126 and CRK expression in gastric cancer
title_short Prognostic value of microRNA-126 and CRK expression in gastric cancer
title_sort prognostic value of microrna-126 and crk expression in gastric cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066993/
https://www.ncbi.nlm.nih.gov/pubmed/27785060
http://dx.doi.org/10.2147/OTT.S87778
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