ILs-3, 6 and 11 increase, but ILs-10 and 24 decrease stemness of human prostate cancer cells in vitro

Cancer stem cells (CSCs) are associated with cancer recurrence and metastasis. Prostate cancer cells often metastasize to the bone with a complex microenvironment of cytokines favoring cell survival. In this study, the cell stemness influence of a group of interleukins including IL-3, 6, 10, 11 and...

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Main Authors: Yu, Dandan, Zhong, Yali, Li, Xiaoran, Li, Yaqing, Li, Xiaoli, Cao, Jing, Fan, Huijie, Yuan, Yuan, Ji, Zhenyu, Qiao, Baoping, Wen, Jian-Guo, Zhang, Mingzhi, Kvalheim, Gunnar, Nesland, Jahn M., Suo, Zhenhe
Format: Online
Language:English
Published: Impact Journals LLC 2015
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4767463/
id pubmed-4767463
recordtype oai_dc
spelling pubmed-47674632016-03-25 ILs-3, 6 and 11 increase, but ILs-10 and 24 decrease stemness of human prostate cancer cells in vitro Yu, Dandan Zhong, Yali Li, Xiaoran Li, Yaqing Li, Xiaoli Cao, Jing Fan, Huijie Yuan, Yuan Ji, Zhenyu Qiao, Baoping Wen, Jian-Guo Zhang, Mingzhi Kvalheim, Gunnar Nesland, Jahn M. Suo, Zhenhe Research Paper Cancer stem cells (CSCs) are associated with cancer recurrence and metastasis. Prostate cancer cells often metastasize to the bone with a complex microenvironment of cytokines favoring cell survival. In this study, the cell stemness influence of a group of interleukins including IL-3, 6, 10, 11 and 24 on human prostate cancer cell lines LNCaP and PC-3 was explored in vitro. Sulforhodamine B(SRB) and 5-ethynyl-2′-deoxyuridine (EdU) assays were applied to examine the effect on cell proliferation, and wound healing and transwell assays were used for migration and invasion studies, in addition to colony formation, Western blotting and flowcytometry for the expression of stemness factors and chemotherapy sensitivity. We observed that ILs-3, 6 and 11 stimulated while ILs-10 and 24 inhibited the growth, invasion and migration of both cell lines. Interestingly, ILs-3, 6 and 11 significantly promoted colony formation and increased the expression of SOX2, CD44 and ABCG2 in both prostate cancer cell lines. However, ILs-10 and 24 showed the opposite effect on the expression of these factors. In line with the above findings, treatment with either IL-3 or IL-6 or IL-11 decreased the chemosensitivity to docetaxel while treatment with either IL-10 or IL-24 increased the sensitivity of docetaxel chemotherapy. In conclusion, our results suggest that ILs-3, 6 and 11 function as tumor promoters while ILs-10 and 24 function as tumor suppressors in the prostate cancer cell lines PC-3 and LNCaP in vitro, and such differences may attribute to their different effect on the stemness of PCa cells. Impact Journals LLC 2015-10-21 /pmc/articles/PMC4767463/ /pubmed/26528857 Text en Copyright: © 2015 Yu et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Yu, Dandan
Zhong, Yali
Li, Xiaoran
Li, Yaqing
Li, Xiaoli
Cao, Jing
Fan, Huijie
Yuan, Yuan
Ji, Zhenyu
Qiao, Baoping
Wen, Jian-Guo
Zhang, Mingzhi
Kvalheim, Gunnar
Nesland, Jahn M.
Suo, Zhenhe
spellingShingle Yu, Dandan
Zhong, Yali
Li, Xiaoran
Li, Yaqing
Li, Xiaoli
Cao, Jing
Fan, Huijie
Yuan, Yuan
Ji, Zhenyu
Qiao, Baoping
Wen, Jian-Guo
Zhang, Mingzhi
Kvalheim, Gunnar
Nesland, Jahn M.
Suo, Zhenhe
ILs-3, 6 and 11 increase, but ILs-10 and 24 decrease stemness of human prostate cancer cells in vitro
author_facet Yu, Dandan
Zhong, Yali
Li, Xiaoran
Li, Yaqing
Li, Xiaoli
Cao, Jing
Fan, Huijie
Yuan, Yuan
Ji, Zhenyu
Qiao, Baoping
Wen, Jian-Guo
Zhang, Mingzhi
Kvalheim, Gunnar
Nesland, Jahn M.
Suo, Zhenhe
author_sort Yu, Dandan
title ILs-3, 6 and 11 increase, but ILs-10 and 24 decrease stemness of human prostate cancer cells in vitro
title_short ILs-3, 6 and 11 increase, but ILs-10 and 24 decrease stemness of human prostate cancer cells in vitro
title_full ILs-3, 6 and 11 increase, but ILs-10 and 24 decrease stemness of human prostate cancer cells in vitro
title_fullStr ILs-3, 6 and 11 increase, but ILs-10 and 24 decrease stemness of human prostate cancer cells in vitro
title_full_unstemmed ILs-3, 6 and 11 increase, but ILs-10 and 24 decrease stemness of human prostate cancer cells in vitro
title_sort ils-3, 6 and 11 increase, but ils-10 and 24 decrease stemness of human prostate cancer cells in vitro
description Cancer stem cells (CSCs) are associated with cancer recurrence and metastasis. Prostate cancer cells often metastasize to the bone with a complex microenvironment of cytokines favoring cell survival. In this study, the cell stemness influence of a group of interleukins including IL-3, 6, 10, 11 and 24 on human prostate cancer cell lines LNCaP and PC-3 was explored in vitro. Sulforhodamine B(SRB) and 5-ethynyl-2′-deoxyuridine (EdU) assays were applied to examine the effect on cell proliferation, and wound healing and transwell assays were used for migration and invasion studies, in addition to colony formation, Western blotting and flowcytometry for the expression of stemness factors and chemotherapy sensitivity. We observed that ILs-3, 6 and 11 stimulated while ILs-10 and 24 inhibited the growth, invasion and migration of both cell lines. Interestingly, ILs-3, 6 and 11 significantly promoted colony formation and increased the expression of SOX2, CD44 and ABCG2 in both prostate cancer cell lines. However, ILs-10 and 24 showed the opposite effect on the expression of these factors. In line with the above findings, treatment with either IL-3 or IL-6 or IL-11 decreased the chemosensitivity to docetaxel while treatment with either IL-10 or IL-24 increased the sensitivity of docetaxel chemotherapy. In conclusion, our results suggest that ILs-3, 6 and 11 function as tumor promoters while ILs-10 and 24 function as tumor suppressors in the prostate cancer cell lines PC-3 and LNCaP in vitro, and such differences may attribute to their different effect on the stemness of PCa cells.
publisher Impact Journals LLC
publishDate 2015
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4767463/
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