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CDKN3 expression predicates poor prognosis and regulates adriamycin sensitivity in hepatocellular carcinoma in vitro
OBJECTIVE: Hepatocellular carcinoma (HCC) is one of the most common causes of cancer-related deaths worldwide. This study investigated the relationship between cyclin-dependent kinase inhibitor (CDKN)3 and prognosis and pathological characteristics in HCC patients to determine whether it could be us...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7388118/ https://www.ncbi.nlm.nih.gov/pubmed/32721244 http://dx.doi.org/10.1177/0300060520936879 |
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author | Dai, Wei Fang, Shuo Cai, Guanhe Dai, Jialiang Lin, Guotai Ye, Qiurong Miao, Huilai Chen, Ming Tan, Xiaoyu Chen, Nianping Liu, Xiaoguang Li, Mingyi |
author_facet | Dai, Wei Fang, Shuo Cai, Guanhe Dai, Jialiang Lin, Guotai Ye, Qiurong Miao, Huilai Chen, Ming Tan, Xiaoyu Chen, Nianping Liu, Xiaoguang Li, Mingyi |
author_sort | Dai, Wei |
collection | PubMed |
description | OBJECTIVE: Hepatocellular carcinoma (HCC) is one of the most common causes of cancer-related deaths worldwide. This study investigated the relationship between cyclin-dependent kinase inhibitor (CDKN)3 and prognosis and pathological characteristics in HCC patients to determine whether it could be used as a prognostic factor and/or therapeutic target for HCC drug development. METHODS: We previously showed that CDKN3 is deregulated in HCC tumor samples. Here, bioinformatics analysis was used to assess the relationship between CDKN3 gene expression and the characteristics of HCC patients from Gene Expression Omnibus and The Cancer Genome Atlas databases. Additionally, CDKN3 expression was silenced by small interfering RNA to determine its effect on HCC cell proliferation and on HCC cell sensitivity to adriamycin chemotherapy. RESULTS: Bioinformatics analysis showed a negative correlation between CDKN3 expression and both disease-free survival and overall survival. CDKN3 silencing did not significantly suppress the proliferation of HCC cells, but did decrease their sensitivity to adriamycin. CONCLUSIONS: CDKN3 may have a dual role during the development of HCC, and could be used as an independent prognostic factor and therapeutic target for HCC treatment. |
format | Online Article Text |
id | pubmed-7388118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-73881182020-08-10 CDKN3 expression predicates poor prognosis and regulates adriamycin sensitivity in hepatocellular carcinoma in vitro Dai, Wei Fang, Shuo Cai, Guanhe Dai, Jialiang Lin, Guotai Ye, Qiurong Miao, Huilai Chen, Ming Tan, Xiaoyu Chen, Nianping Liu, Xiaoguang Li, Mingyi J Int Med Res Retrospective Clinical Research Report OBJECTIVE: Hepatocellular carcinoma (HCC) is one of the most common causes of cancer-related deaths worldwide. This study investigated the relationship between cyclin-dependent kinase inhibitor (CDKN)3 and prognosis and pathological characteristics in HCC patients to determine whether it could be used as a prognostic factor and/or therapeutic target for HCC drug development. METHODS: We previously showed that CDKN3 is deregulated in HCC tumor samples. Here, bioinformatics analysis was used to assess the relationship between CDKN3 gene expression and the characteristics of HCC patients from Gene Expression Omnibus and The Cancer Genome Atlas databases. Additionally, CDKN3 expression was silenced by small interfering RNA to determine its effect on HCC cell proliferation and on HCC cell sensitivity to adriamycin chemotherapy. RESULTS: Bioinformatics analysis showed a negative correlation between CDKN3 expression and both disease-free survival and overall survival. CDKN3 silencing did not significantly suppress the proliferation of HCC cells, but did decrease their sensitivity to adriamycin. CONCLUSIONS: CDKN3 may have a dual role during the development of HCC, and could be used as an independent prognostic factor and therapeutic target for HCC treatment. SAGE Publications 2020-07-28 /pmc/articles/PMC7388118/ /pubmed/32721244 http://dx.doi.org/10.1177/0300060520936879 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Retrospective Clinical Research Report Dai, Wei Fang, Shuo Cai, Guanhe Dai, Jialiang Lin, Guotai Ye, Qiurong Miao, Huilai Chen, Ming Tan, Xiaoyu Chen, Nianping Liu, Xiaoguang Li, Mingyi CDKN3 expression predicates poor prognosis and regulates adriamycin sensitivity in hepatocellular carcinoma in vitro |
title | CDKN3 expression predicates poor prognosis and regulates adriamycin
sensitivity in hepatocellular carcinoma in
vitro |
title_full | CDKN3 expression predicates poor prognosis and regulates adriamycin
sensitivity in hepatocellular carcinoma in
vitro |
title_fullStr | CDKN3 expression predicates poor prognosis and regulates adriamycin
sensitivity in hepatocellular carcinoma in
vitro |
title_full_unstemmed | CDKN3 expression predicates poor prognosis and regulates adriamycin
sensitivity in hepatocellular carcinoma in
vitro |
title_short | CDKN3 expression predicates poor prognosis and regulates adriamycin
sensitivity in hepatocellular carcinoma in
vitro |
title_sort | cdkn3 expression predicates poor prognosis and regulates adriamycin
sensitivity in hepatocellular carcinoma in
vitro |
topic | Retrospective Clinical Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7388118/ https://www.ncbi.nlm.nih.gov/pubmed/32721244 http://dx.doi.org/10.1177/0300060520936879 |
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