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NHERF1 Enhances Cisplatin Sensitivity in Human Cervical Cancer Cells
Cervical cancer is one of the most common female malignancies, and cisplatin-based chemotherapy is routinely utilized in locally advanced cervical cancer patients. However, resistance has been the major limitation. In this study, we found that Na(+)/H(+) Exchanger Regulatory Factor 1 (NHERF1) was do...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297640/ https://www.ncbi.nlm.nih.gov/pubmed/28085111 http://dx.doi.org/10.3390/ijms18010005 |
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author | Tao, Tao Yang, Xiaomei Qin, Qiong Shi, Wen Wang, Qiqi Yang, Ying He, Junqi |
author_facet | Tao, Tao Yang, Xiaomei Qin, Qiong Shi, Wen Wang, Qiqi Yang, Ying He, Junqi |
author_sort | Tao, Tao |
collection | PubMed |
description | Cervical cancer is one of the most common female malignancies, and cisplatin-based chemotherapy is routinely utilized in locally advanced cervical cancer patients. However, resistance has been the major limitation. In this study, we found that Na(+)/H(+) Exchanger Regulatory Factor 1 (NHERF1) was downregulated in cisplatin-resistant cells. Analysis based on a cervical cancer dataset from The Cancer Genome Atlas (TCGA) showed association of NHERF1 expression with disease-free survival of patients received cisplatin treatment. NHERF1 overexpression inhibited proliferation and enhanced apoptosis in cisplatin-resistant HeLa cells, whereas NHERF1 knockdown had inverse effects. While parental HeLa cells were more resistant to cisplatin after NHERF1 knockdown, NHERF1 overexpression in CaSki cells promoted cisplatin sensitivity. Overexpression and knockdown studies also showed that NHERF1 significantly inhibited AKT and extracellular signal–regulated kinase (ERK) signaling pathways in cisplatin-resistant cells. Taken together, our results provide the first evidence that NHERF1 can sensitize cisplatin-refractory cervical cancer cells. This study may help to increase understanding of the molecular mechanisms underlying cisplatin resistance in tumors. |
format | Online Article Text |
id | pubmed-5297640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-52976402017-02-10 NHERF1 Enhances Cisplatin Sensitivity in Human Cervical Cancer Cells Tao, Tao Yang, Xiaomei Qin, Qiong Shi, Wen Wang, Qiqi Yang, Ying He, Junqi Int J Mol Sci Article Cervical cancer is one of the most common female malignancies, and cisplatin-based chemotherapy is routinely utilized in locally advanced cervical cancer patients. However, resistance has been the major limitation. In this study, we found that Na(+)/H(+) Exchanger Regulatory Factor 1 (NHERF1) was downregulated in cisplatin-resistant cells. Analysis based on a cervical cancer dataset from The Cancer Genome Atlas (TCGA) showed association of NHERF1 expression with disease-free survival of patients received cisplatin treatment. NHERF1 overexpression inhibited proliferation and enhanced apoptosis in cisplatin-resistant HeLa cells, whereas NHERF1 knockdown had inverse effects. While parental HeLa cells were more resistant to cisplatin after NHERF1 knockdown, NHERF1 overexpression in CaSki cells promoted cisplatin sensitivity. Overexpression and knockdown studies also showed that NHERF1 significantly inhibited AKT and extracellular signal–regulated kinase (ERK) signaling pathways in cisplatin-resistant cells. Taken together, our results provide the first evidence that NHERF1 can sensitize cisplatin-refractory cervical cancer cells. This study may help to increase understanding of the molecular mechanisms underlying cisplatin resistance in tumors. MDPI 2017-01-12 /pmc/articles/PMC5297640/ /pubmed/28085111 http://dx.doi.org/10.3390/ijms18010005 Text en © 2017 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Tao, Tao Yang, Xiaomei Qin, Qiong Shi, Wen Wang, Qiqi Yang, Ying He, Junqi NHERF1 Enhances Cisplatin Sensitivity in Human Cervical Cancer Cells |
title | NHERF1 Enhances Cisplatin Sensitivity in Human Cervical Cancer Cells |
title_full | NHERF1 Enhances Cisplatin Sensitivity in Human Cervical Cancer Cells |
title_fullStr | NHERF1 Enhances Cisplatin Sensitivity in Human Cervical Cancer Cells |
title_full_unstemmed | NHERF1 Enhances Cisplatin Sensitivity in Human Cervical Cancer Cells |
title_short | NHERF1 Enhances Cisplatin Sensitivity in Human Cervical Cancer Cells |
title_sort | nherf1 enhances cisplatin sensitivity in human cervical cancer cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297640/ https://www.ncbi.nlm.nih.gov/pubmed/28085111 http://dx.doi.org/10.3390/ijms18010005 |
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