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Low expression of RecQ-like helicase 5 is associated with poor prognosis in patients with gastric cancer
The role of RecQ-like helicase 5 (RECQL5) in gastric cancer (GC) is unclear. This study investigated the expression, clinicopathological association and prognosis of RECQL5 protein in human GC. Firstly, the Oncomine database was used to determine the mRNA expression levels of RECQL5 in GC samples. G...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6924161/ https://www.ncbi.nlm.nih.gov/pubmed/31897211 http://dx.doi.org/10.3892/ol.2019.11137 |
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author | Lin, Yijia Wang, Huashe Wang, Xinyou Li, Miao Chen, Honglei Peng, Junsheng |
author_facet | Lin, Yijia Wang, Huashe Wang, Xinyou Li, Miao Chen, Honglei Peng, Junsheng |
author_sort | Lin, Yijia |
collection | PubMed |
description | The role of RecQ-like helicase 5 (RECQL5) in gastric cancer (GC) is unclear. This study investigated the expression, clinicopathological association and prognosis of RECQL5 protein in human GC. Firstly, the Oncomine database was used to determine the mRNA expression levels of RECQL5 in GC samples. GC samples and adjacent normal gastric tissue samples were subsequently assessed to determine RECQL5 protein expression levels using immunohistochemistry. The clinicopathological association with RECQL5 expression was analyzed. Multivariate Cox analysis was performed to determine the relationship between RECQL5 expression and survival outcomes. Data from the Oncomine database revealed that RECQL5 mRNA was significantly downregulated in GC tissues compared with that in normal gastric tissues (P<0.05). These results were then validated at the protein level as RECQL5 protein expression was found to be significantly downregulated in GC samples compared with that in normal gastric tissues (P<0.05). Low expression of RECQL5 was significantly associated with depth of tumor invasion, histological differentiation and TNM stage (all P<0.05) and indicated poor prognosis in patients with GC. Multivariate analysis revealed that low RECQL5 expression and depth of invasion were independent prognostic factors for GC (P<0.05). These results suggest that low expression of RECQL5 is associated with carcinogenesis and invasion in GC and with poor overall survival in patients with GC. RECQL5 may be a novel prognostic marker for patients with GC. |
format | Online Article Text |
id | pubmed-6924161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-69241612020-01-02 Low expression of RecQ-like helicase 5 is associated with poor prognosis in patients with gastric cancer Lin, Yijia Wang, Huashe Wang, Xinyou Li, Miao Chen, Honglei Peng, Junsheng Oncol Lett Articles The role of RecQ-like helicase 5 (RECQL5) in gastric cancer (GC) is unclear. This study investigated the expression, clinicopathological association and prognosis of RECQL5 protein in human GC. Firstly, the Oncomine database was used to determine the mRNA expression levels of RECQL5 in GC samples. GC samples and adjacent normal gastric tissue samples were subsequently assessed to determine RECQL5 protein expression levels using immunohistochemistry. The clinicopathological association with RECQL5 expression was analyzed. Multivariate Cox analysis was performed to determine the relationship between RECQL5 expression and survival outcomes. Data from the Oncomine database revealed that RECQL5 mRNA was significantly downregulated in GC tissues compared with that in normal gastric tissues (P<0.05). These results were then validated at the protein level as RECQL5 protein expression was found to be significantly downregulated in GC samples compared with that in normal gastric tissues (P<0.05). Low expression of RECQL5 was significantly associated with depth of tumor invasion, histological differentiation and TNM stage (all P<0.05) and indicated poor prognosis in patients with GC. Multivariate analysis revealed that low RECQL5 expression and depth of invasion were independent prognostic factors for GC (P<0.05). These results suggest that low expression of RECQL5 is associated with carcinogenesis and invasion in GC and with poor overall survival in patients with GC. RECQL5 may be a novel prognostic marker for patients with GC. D.A. Spandidos 2020-01 2019-11-21 /pmc/articles/PMC6924161/ /pubmed/31897211 http://dx.doi.org/10.3892/ol.2019.11137 Text en Copyright: © Lin et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Articles Lin, Yijia Wang, Huashe Wang, Xinyou Li, Miao Chen, Honglei Peng, Junsheng Low expression of RecQ-like helicase 5 is associated with poor prognosis in patients with gastric cancer |
title | Low expression of RecQ-like helicase 5 is associated with poor prognosis in patients with gastric cancer |
title_full | Low expression of RecQ-like helicase 5 is associated with poor prognosis in patients with gastric cancer |
title_fullStr | Low expression of RecQ-like helicase 5 is associated with poor prognosis in patients with gastric cancer |
title_full_unstemmed | Low expression of RecQ-like helicase 5 is associated with poor prognosis in patients with gastric cancer |
title_short | Low expression of RecQ-like helicase 5 is associated with poor prognosis in patients with gastric cancer |
title_sort | low expression of recq-like helicase 5 is associated with poor prognosis in patients with gastric cancer |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6924161/ https://www.ncbi.nlm.nih.gov/pubmed/31897211 http://dx.doi.org/10.3892/ol.2019.11137 |
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