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GAS8 and GAS8-AS1 expression in gastric cancer

AIM: To evaluate the expression of the growth arrest-specific 8 (GAS8) and its antisense (GAS8-AS1) in gastric cancer. BACKGROUND: GAS8 exists in a genomic region that is recurrently deleted in breast and prostate cancer. This gene contains a long non-coding RNA, namely GAS8-AS1 whose roles in the r...

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Autores principales: Esfandi, Farbod, Mohammad Rezaei, Fatemeh, Taheri, Mohammad, Naby Gol, Maryam, Kholghi Oskooei, Vahid, Namvar, Amir, Ghafouri-Fard, Soudeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820832/
https://www.ncbi.nlm.nih.gov/pubmed/31749921
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author Esfandi, Farbod
Mohammad Rezaei, Fatemeh
Taheri, Mohammad
Naby Gol, Maryam
Kholghi Oskooei, Vahid
Namvar, Amir
Ghafouri-Fard, Soudeh
author_facet Esfandi, Farbod
Mohammad Rezaei, Fatemeh
Taheri, Mohammad
Naby Gol, Maryam
Kholghi Oskooei, Vahid
Namvar, Amir
Ghafouri-Fard, Soudeh
author_sort Esfandi, Farbod
collection PubMed
description AIM: To evaluate the expression of the growth arrest-specific 8 (GAS8) and its antisense (GAS8-AS1) in gastric cancer. BACKGROUND: GAS8 exists in a genomic region that is recurrently deleted in breast and prostate cancer. This gene contains a long non-coding RNA, namely GAS8-AS1 whose roles in the regulation of GAS8 has been reported in hepatocytes. GAS8-AS1 has also been regarded as a putative tumor suppressor gene in papillary thyroid cancer and hepatocellular carcinoma. METHODS: In the present study, we evaluated expression levels of GAS8 and GAS8-AS1 in 30 gastric cancer tissues and their corresponding adjacent non-cancerous tissues (ANCTs). RESULTS: GAS8 was significantly down-regulated in tumor tissues compared to ANCTs (Expression ratio=0.29, p<0.001). Although the expression of GAS8-AS1 was higher in tumor tissues compared to ANCTs (Expression ratio=2.15), it did not reach the level of significance (p=0.12). GAS8 expression was associated with the site of the primary tumor (p=0.01). GAS8-AS1 expression was significantly higher in tumors with lymphatic/ vascular invasion compared with those without lymphatic/ vascular invasion (p=0.03). Significant pairwise correlations were detected between expression levels of GAS8 and GAS8-AS1 in tumor tissues and ANCTs. Based on the results of the ROC curve, the diagnostic power of transcript levels of GAS8 in gastric tissues was estimated to be 76%. CONCLUSION: The current study underscores the roles of GAS8 and GAS8-AS1 in gastric carcinogenesis and warrants future functional studies to unravel the underlying mechanism of such contribution.
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spelling pubmed-68208322019-11-20 GAS8 and GAS8-AS1 expression in gastric cancer Esfandi, Farbod Mohammad Rezaei, Fatemeh Taheri, Mohammad Naby Gol, Maryam Kholghi Oskooei, Vahid Namvar, Amir Ghafouri-Fard, Soudeh Gastroenterol Hepatol Bed Bench Original Article AIM: To evaluate the expression of the growth arrest-specific 8 (GAS8) and its antisense (GAS8-AS1) in gastric cancer. BACKGROUND: GAS8 exists in a genomic region that is recurrently deleted in breast and prostate cancer. This gene contains a long non-coding RNA, namely GAS8-AS1 whose roles in the regulation of GAS8 has been reported in hepatocytes. GAS8-AS1 has also been regarded as a putative tumor suppressor gene in papillary thyroid cancer and hepatocellular carcinoma. METHODS: In the present study, we evaluated expression levels of GAS8 and GAS8-AS1 in 30 gastric cancer tissues and their corresponding adjacent non-cancerous tissues (ANCTs). RESULTS: GAS8 was significantly down-regulated in tumor tissues compared to ANCTs (Expression ratio=0.29, p<0.001). Although the expression of GAS8-AS1 was higher in tumor tissues compared to ANCTs (Expression ratio=2.15), it did not reach the level of significance (p=0.12). GAS8 expression was associated with the site of the primary tumor (p=0.01). GAS8-AS1 expression was significantly higher in tumors with lymphatic/ vascular invasion compared with those without lymphatic/ vascular invasion (p=0.03). Significant pairwise correlations were detected between expression levels of GAS8 and GAS8-AS1 in tumor tissues and ANCTs. Based on the results of the ROC curve, the diagnostic power of transcript levels of GAS8 in gastric tissues was estimated to be 76%. CONCLUSION: The current study underscores the roles of GAS8 and GAS8-AS1 in gastric carcinogenesis and warrants future functional studies to unravel the underlying mechanism of such contribution. Shaheed Beheshti University of Medical Sciences 2019 /pmc/articles/PMC6820832/ /pubmed/31749921 Text en ©2019 RIGLD, Research Institute for Gastroenterology and Liver Diseases This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Esfandi, Farbod
Mohammad Rezaei, Fatemeh
Taheri, Mohammad
Naby Gol, Maryam
Kholghi Oskooei, Vahid
Namvar, Amir
Ghafouri-Fard, Soudeh
GAS8 and GAS8-AS1 expression in gastric cancer
title GAS8 and GAS8-AS1 expression in gastric cancer
title_full GAS8 and GAS8-AS1 expression in gastric cancer
title_fullStr GAS8 and GAS8-AS1 expression in gastric cancer
title_full_unstemmed GAS8 and GAS8-AS1 expression in gastric cancer
title_short GAS8 and GAS8-AS1 expression in gastric cancer
title_sort gas8 and gas8-as1 expression in gastric cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820832/
https://www.ncbi.nlm.nih.gov/pubmed/31749921
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