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ALDH1 might influence the metastatic capability of HeLa cells

Recent data suggest that tumor persistence and recurrence could be caused by the presence of cancer stem cells (CSCs). Aldehyde dehydrogenase 1 (ALDH1) has been implicated in cancer pathogenesis and used as a CSC marker. We previously reported that cervical carcinoma contains a small subpopulation o...

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Autores principales: Yao, Tingting, Lu, Rongbiao, Li, Yiqing, Peng, Yongpai, Ding, Miao, Xie, Xiaofei, Lin, Zhongqiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4644206/
https://www.ncbi.nlm.nih.gov/pubmed/25864109
http://dx.doi.org/10.1007/s13277-015-3398-y
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author Yao, Tingting
Lu, Rongbiao
Li, Yiqing
Peng, Yongpai
Ding, Miao
Xie, Xiaofei
Lin, Zhongqiu
author_facet Yao, Tingting
Lu, Rongbiao
Li, Yiqing
Peng, Yongpai
Ding, Miao
Xie, Xiaofei
Lin, Zhongqiu
author_sort Yao, Tingting
collection PubMed
description Recent data suggest that tumor persistence and recurrence could be caused by the presence of cancer stem cells (CSCs). Aldehyde dehydrogenase 1 (ALDH1) has been implicated in cancer pathogenesis and used as a CSC marker. We previously reported that cervical carcinoma contains a small subpopulation of cells expressing ALDH1 [1]. In this study, we used small interfering RNA to suppress ALDH1 expression and introduced an ALDH1 reporting vector into HeLa cells followed by various in vitro assays. We showed that knockdown of ALDH1 expression reduced the cell migration ability of HeLa cells, whereas augmented expression of ALDH1 increased cell migration. However, there was no difference in the cellular proliferation, apoptosis, cell cycle, and invasion. These results indicate that ALDH1 is directly involved in HeLa migration.
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spelling pubmed-46442062015-11-24 ALDH1 might influence the metastatic capability of HeLa cells Yao, Tingting Lu, Rongbiao Li, Yiqing Peng, Yongpai Ding, Miao Xie, Xiaofei Lin, Zhongqiu Tumour Biol Research Article Recent data suggest that tumor persistence and recurrence could be caused by the presence of cancer stem cells (CSCs). Aldehyde dehydrogenase 1 (ALDH1) has been implicated in cancer pathogenesis and used as a CSC marker. We previously reported that cervical carcinoma contains a small subpopulation of cells expressing ALDH1 [1]. In this study, we used small interfering RNA to suppress ALDH1 expression and introduced an ALDH1 reporting vector into HeLa cells followed by various in vitro assays. We showed that knockdown of ALDH1 expression reduced the cell migration ability of HeLa cells, whereas augmented expression of ALDH1 increased cell migration. However, there was no difference in the cellular proliferation, apoptosis, cell cycle, and invasion. These results indicate that ALDH1 is directly involved in HeLa migration. Springer Netherlands 2015-04-13 /pmc/articles/PMC4644206/ /pubmed/25864109 http://dx.doi.org/10.1007/s13277-015-3398-y Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Article
Yao, Tingting
Lu, Rongbiao
Li, Yiqing
Peng, Yongpai
Ding, Miao
Xie, Xiaofei
Lin, Zhongqiu
ALDH1 might influence the metastatic capability of HeLa cells
title ALDH1 might influence the metastatic capability of HeLa cells
title_full ALDH1 might influence the metastatic capability of HeLa cells
title_fullStr ALDH1 might influence the metastatic capability of HeLa cells
title_full_unstemmed ALDH1 might influence the metastatic capability of HeLa cells
title_short ALDH1 might influence the metastatic capability of HeLa cells
title_sort aldh1 might influence the metastatic capability of hela cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4644206/
https://www.ncbi.nlm.nih.gov/pubmed/25864109
http://dx.doi.org/10.1007/s13277-015-3398-y
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