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PRDM5 promotes the proliferation and invasion of murine melanoma cells through up‐regulating JNK expression

PRDM (PRDI‐BF1 and RIZ domain‐containing) proteins constitute a family of zinc finger proteins and play important roles in multiple cellular processes by acting as epigenetic modifiers. PRDM5 is a recently identified member of the PRDM family and may function as a tumor suppressor in several types o...

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Autores principales: Wang, Lei, Ding, Qiong‐Qiong, Gao, Shan‐Shan, Yang, Hai‐Jie, Wang, Mian, Shi, Yu, Cheng, Bin‐Feng, Bi, Jia‐Jia, Feng, Zhi‐Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5055150/
https://www.ncbi.nlm.nih.gov/pubmed/27485778
http://dx.doi.org/10.1002/cam4.846
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author Wang, Lei
Ding, Qiong‐Qiong
Gao, Shan‐Shan
Yang, Hai‐Jie
Wang, Mian
Shi, Yu
Cheng, Bin‐Feng
Bi, Jia‐Jia
Feng, Zhi‐Wei
author_facet Wang, Lei
Ding, Qiong‐Qiong
Gao, Shan‐Shan
Yang, Hai‐Jie
Wang, Mian
Shi, Yu
Cheng, Bin‐Feng
Bi, Jia‐Jia
Feng, Zhi‐Wei
author_sort Wang, Lei
collection PubMed
description PRDM (PRDI‐BF1 and RIZ domain‐containing) proteins constitute a family of zinc finger proteins and play important roles in multiple cellular processes by acting as epigenetic modifiers. PRDM5 is a recently identified member of the PRDM family and may function as a tumor suppressor in several types of cancer. However, the role of PRDM5 in murine melanoma remains largely unknown. In our study, effect of PRDM5 on murine melanoma cells was determined and results showed that PRDM5 overexpression significantly promoted proliferation, migration, and invasion of murine melanoma B16F10 cells. Consistently, silencing of PRDM5 expression significantly inhibited proliferation, invasion, and migration of B16F10 cells. In vivo study also showed that PRDM5 silencing significantly inhibited the growth and metastasis of melanoma in mice. PRDM5 was then found to increase the expression and activation of JNK in B16F10 cells. JNK silencing significantly reduced PRDM5‐mediated up‐regulation of JNK expression and blocked the PRDM5‐induced proliferation and invasion of B16F10 cells. To further verify the involvement of JNK signaling in PRDM5‐induced progression of B16F10 cells, a specific JNK inhibitor was employed to inhibit the JNK signaling pathway, and results showed that PRDM5‐induced proliferation and invasion of B16F10 cells were abolished. We conclude that PRDM5 promotes the proliferation and invasion of murine melanoma cells through up‐regulating JNK expression and strategies targeting PRDM5 may be promising for the therapy of melanoma.
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spelling pubmed-50551502016-12-12 PRDM5 promotes the proliferation and invasion of murine melanoma cells through up‐regulating JNK expression Wang, Lei Ding, Qiong‐Qiong Gao, Shan‐Shan Yang, Hai‐Jie Wang, Mian Shi, Yu Cheng, Bin‐Feng Bi, Jia‐Jia Feng, Zhi‐Wei Cancer Med Cancer Biology PRDM (PRDI‐BF1 and RIZ domain‐containing) proteins constitute a family of zinc finger proteins and play important roles in multiple cellular processes by acting as epigenetic modifiers. PRDM5 is a recently identified member of the PRDM family and may function as a tumor suppressor in several types of cancer. However, the role of PRDM5 in murine melanoma remains largely unknown. In our study, effect of PRDM5 on murine melanoma cells was determined and results showed that PRDM5 overexpression significantly promoted proliferation, migration, and invasion of murine melanoma B16F10 cells. Consistently, silencing of PRDM5 expression significantly inhibited proliferation, invasion, and migration of B16F10 cells. In vivo study also showed that PRDM5 silencing significantly inhibited the growth and metastasis of melanoma in mice. PRDM5 was then found to increase the expression and activation of JNK in B16F10 cells. JNK silencing significantly reduced PRDM5‐mediated up‐regulation of JNK expression and blocked the PRDM5‐induced proliferation and invasion of B16F10 cells. To further verify the involvement of JNK signaling in PRDM5‐induced progression of B16F10 cells, a specific JNK inhibitor was employed to inhibit the JNK signaling pathway, and results showed that PRDM5‐induced proliferation and invasion of B16F10 cells were abolished. We conclude that PRDM5 promotes the proliferation and invasion of murine melanoma cells through up‐regulating JNK expression and strategies targeting PRDM5 may be promising for the therapy of melanoma. John Wiley and Sons Inc. 2016-08-03 /pmc/articles/PMC5055150/ /pubmed/27485778 http://dx.doi.org/10.1002/cam4.846 Text en © 2016 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cancer Biology
Wang, Lei
Ding, Qiong‐Qiong
Gao, Shan‐Shan
Yang, Hai‐Jie
Wang, Mian
Shi, Yu
Cheng, Bin‐Feng
Bi, Jia‐Jia
Feng, Zhi‐Wei
PRDM5 promotes the proliferation and invasion of murine melanoma cells through up‐regulating JNK expression
title PRDM5 promotes the proliferation and invasion of murine melanoma cells through up‐regulating JNK expression
title_full PRDM5 promotes the proliferation and invasion of murine melanoma cells through up‐regulating JNK expression
title_fullStr PRDM5 promotes the proliferation and invasion of murine melanoma cells through up‐regulating JNK expression
title_full_unstemmed PRDM5 promotes the proliferation and invasion of murine melanoma cells through up‐regulating JNK expression
title_short PRDM5 promotes the proliferation and invasion of murine melanoma cells through up‐regulating JNK expression
title_sort prdm5 promotes the proliferation and invasion of murine melanoma cells through up‐regulating jnk expression
topic Cancer Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5055150/
https://www.ncbi.nlm.nih.gov/pubmed/27485778
http://dx.doi.org/10.1002/cam4.846
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