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The association between KLF4 as a tumor suppressor and the prognosis of hepatocellular carcinoma after curative resection
Krüppel-like factor 4 (KLF4), a zinc-finger transcription factor in klfs family, is known for its crucial role in regulating cell growth, proliferation, and differentiation. This research aimed to explore the prognostic significance of KLF4 in hepatocellular carcinoma’s (HCC) patients after curative...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7467357/ https://www.ncbi.nlm.nih.gov/pubmed/32756012 http://dx.doi.org/10.18632/aging.103592 |
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author | Xue, Min Zhou, Chenhao Zheng, Yan Zhang, Ziping Wang, Shun Fu, Yan Atyah, Manar Xue, Xiaolong Zhu, Le Dong, Qiongzhu Jia, Huliang Ren, Ning Hu, Ruolei |
author_facet | Xue, Min Zhou, Chenhao Zheng, Yan Zhang, Ziping Wang, Shun Fu, Yan Atyah, Manar Xue, Xiaolong Zhu, Le Dong, Qiongzhu Jia, Huliang Ren, Ning Hu, Ruolei |
author_sort | Xue, Min |
collection | PubMed |
description | Krüppel-like factor 4 (KLF4), a zinc-finger transcription factor in klfs family, is known for its crucial role in regulating cell growth, proliferation, and differentiation. This research aimed to explore the prognostic significance of KLF4 in hepatocellular carcinoma’s (HCC) patients after curative resection and the role of KLF4 in HCC progression. There were 185 HCC patients who had hepatectomy from July 2010 to July 2011 included in this study. KLF4 expression was detected by microarray immunohistochemical technique, western blot, and qRT-PCR. Then, the correlation between the prognosis of patients and KLF4 expression was evaluated based on patients’ follow-up data. The research found KLF4 expression was significantly downregulated in HCC tissues compared to para-tumorous tissues. More importantly, the overall survival rate (OS) and recurrence-free survival rate (RFS) of HCC patients with low KLF4 expression were both significantly decreased compared to those with a high level of KLF4. Further function and mechanism analysis showed that KLF4 could inhibit the proliferation, migration, invasion and epithelial-mesenchymal transition of HCC cells. The study revealed that KLF4 was not only a tumor suppressor in HCC but also can be regarded as a valuable prognostic factor and potential biological target for diagnosis and treatment in HCC patients. |
format | Online Article Text |
id | pubmed-7467357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-74673572020-09-14 The association between KLF4 as a tumor suppressor and the prognosis of hepatocellular carcinoma after curative resection Xue, Min Zhou, Chenhao Zheng, Yan Zhang, Ziping Wang, Shun Fu, Yan Atyah, Manar Xue, Xiaolong Zhu, Le Dong, Qiongzhu Jia, Huliang Ren, Ning Hu, Ruolei Aging (Albany NY) Research Paper Krüppel-like factor 4 (KLF4), a zinc-finger transcription factor in klfs family, is known for its crucial role in regulating cell growth, proliferation, and differentiation. This research aimed to explore the prognostic significance of KLF4 in hepatocellular carcinoma’s (HCC) patients after curative resection and the role of KLF4 in HCC progression. There were 185 HCC patients who had hepatectomy from July 2010 to July 2011 included in this study. KLF4 expression was detected by microarray immunohistochemical technique, western blot, and qRT-PCR. Then, the correlation between the prognosis of patients and KLF4 expression was evaluated based on patients’ follow-up data. The research found KLF4 expression was significantly downregulated in HCC tissues compared to para-tumorous tissues. More importantly, the overall survival rate (OS) and recurrence-free survival rate (RFS) of HCC patients with low KLF4 expression were both significantly decreased compared to those with a high level of KLF4. Further function and mechanism analysis showed that KLF4 could inhibit the proliferation, migration, invasion and epithelial-mesenchymal transition of HCC cells. The study revealed that KLF4 was not only a tumor suppressor in HCC but also can be regarded as a valuable prognostic factor and potential biological target for diagnosis and treatment in HCC patients. Impact Journals 2020-08-05 /pmc/articles/PMC7467357/ /pubmed/32756012 http://dx.doi.org/10.18632/aging.103592 Text en Copyright © 2020 Xue et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Xue, Min Zhou, Chenhao Zheng, Yan Zhang, Ziping Wang, Shun Fu, Yan Atyah, Manar Xue, Xiaolong Zhu, Le Dong, Qiongzhu Jia, Huliang Ren, Ning Hu, Ruolei The association between KLF4 as a tumor suppressor and the prognosis of hepatocellular carcinoma after curative resection |
title | The association between KLF4 as a tumor suppressor and the prognosis of hepatocellular carcinoma after curative resection |
title_full | The association between KLF4 as a tumor suppressor and the prognosis of hepatocellular carcinoma after curative resection |
title_fullStr | The association between KLF4 as a tumor suppressor and the prognosis of hepatocellular carcinoma after curative resection |
title_full_unstemmed | The association between KLF4 as a tumor suppressor and the prognosis of hepatocellular carcinoma after curative resection |
title_short | The association between KLF4 as a tumor suppressor and the prognosis of hepatocellular carcinoma after curative resection |
title_sort | association between klf4 as a tumor suppressor and the prognosis of hepatocellular carcinoma after curative resection |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7467357/ https://www.ncbi.nlm.nih.gov/pubmed/32756012 http://dx.doi.org/10.18632/aging.103592 |
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