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PIAS3-mediated feedback loops promote chronic colitis-associated malignant transformation

Rationale: Colitis-associated colorectal cancer (CAC) usually exhibits an accelerated disease progression, an increased resistance to therapeutic drugs and a higher mortality rate than sporadic colorectal cancer (CRC). PIAS3 is a member of the protein inhibitor of activated STAT (PIAS) family; howev...

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Autores principales: Ma, Junting, Yang, Yaping, Fu, Yong, Guo, Feilong, Zhang, Xiaoyi, Xiao, Shuke, Zhu, Weiming, Huang, Zhen, Zhang, Junfeng, Chen, Jiangning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996365/
https://www.ncbi.nlm.nih.gov/pubmed/29896300
http://dx.doi.org/10.7150/thno.23046
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author Ma, Junting
Yang, Yaping
Fu, Yong
Guo, Feilong
Zhang, Xiaoyi
Xiao, Shuke
Zhu, Weiming
Huang, Zhen
Zhang, Junfeng
Chen, Jiangning
author_facet Ma, Junting
Yang, Yaping
Fu, Yong
Guo, Feilong
Zhang, Xiaoyi
Xiao, Shuke
Zhu, Weiming
Huang, Zhen
Zhang, Junfeng
Chen, Jiangning
author_sort Ma, Junting
collection PubMed
description Rationale: Colitis-associated colorectal cancer (CAC) usually exhibits an accelerated disease progression, an increased resistance to therapeutic drugs and a higher mortality rate than sporadic colorectal cancer (CRC). PIAS3 is a member of the protein inhibitor of activated STAT (PIAS) family; however, little is known about the expression and biological functions of PIAS3 in CAC. The aim of our study was to investigate the biological mechanisms of PIAS3 in CAC. Methods: PIAS3 expression was examined in colon tissues of CAC/CRC patients and azoxymethane-dextran sulfate sodium (AOM-DSS)-induced mice. The role of PIAS3 was studied using a series of in vitro, in vivo and clinical approaches. Results: Downregulated PIAS3 expression, upregulated miR-18a expression and highly activated NF-κB and STAT3 were observed in colon tissues of CAC/CRC patients and AOM-DSS-induced mice. In vitro experiments revealed that PIAS3 significantly inhibited the activation of NF-κB and STAT3 and demonstrated that activated NF-κB and STAT3 transcriptionally regulated miR-18a level, and up-regulation of miR-18a expression led to defective PIAS3 expression. Moreover, PIAS3-mediated autoregulatory feedback loops (PIAS3/NF-κB/miR-18a and PIAS3/STAT3/miR-18a) were verified in vitro and were found to regulate cell proliferation. Additionally, modulation of the feedback loops via overexpression of PIAS3 or knockdown of miR-18a significantly inhibited cell proliferation in a mouse CRC xenograft model. Furthermore, upregulation of PIAS3 by intracolonic administration of PIAS3 lentivirus or anti-miR-18a lentivirus in AOM-DSS-induced mice led to dramatically reduced tumor sizes/numbers, whereas knockdown of PIAS3 in CAC mice significantly promoted tumor growth. Conclusion: Our data clearly show that PIAS3-mediated feedback loops control cell proliferation and function as robust driving forces for CAC progression. Targeting these highly activated feedback loops might offer promising therapeutic strategies for CAC.
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spelling pubmed-59963652018-06-12 PIAS3-mediated feedback loops promote chronic colitis-associated malignant transformation Ma, Junting Yang, Yaping Fu, Yong Guo, Feilong Zhang, Xiaoyi Xiao, Shuke Zhu, Weiming Huang, Zhen Zhang, Junfeng Chen, Jiangning Theranostics Research Paper Rationale: Colitis-associated colorectal cancer (CAC) usually exhibits an accelerated disease progression, an increased resistance to therapeutic drugs and a higher mortality rate than sporadic colorectal cancer (CRC). PIAS3 is a member of the protein inhibitor of activated STAT (PIAS) family; however, little is known about the expression and biological functions of PIAS3 in CAC. The aim of our study was to investigate the biological mechanisms of PIAS3 in CAC. Methods: PIAS3 expression was examined in colon tissues of CAC/CRC patients and azoxymethane-dextran sulfate sodium (AOM-DSS)-induced mice. The role of PIAS3 was studied using a series of in vitro, in vivo and clinical approaches. Results: Downregulated PIAS3 expression, upregulated miR-18a expression and highly activated NF-κB and STAT3 were observed in colon tissues of CAC/CRC patients and AOM-DSS-induced mice. In vitro experiments revealed that PIAS3 significantly inhibited the activation of NF-κB and STAT3 and demonstrated that activated NF-κB and STAT3 transcriptionally regulated miR-18a level, and up-regulation of miR-18a expression led to defective PIAS3 expression. Moreover, PIAS3-mediated autoregulatory feedback loops (PIAS3/NF-κB/miR-18a and PIAS3/STAT3/miR-18a) were verified in vitro and were found to regulate cell proliferation. Additionally, modulation of the feedback loops via overexpression of PIAS3 or knockdown of miR-18a significantly inhibited cell proliferation in a mouse CRC xenograft model. Furthermore, upregulation of PIAS3 by intracolonic administration of PIAS3 lentivirus or anti-miR-18a lentivirus in AOM-DSS-induced mice led to dramatically reduced tumor sizes/numbers, whereas knockdown of PIAS3 in CAC mice significantly promoted tumor growth. Conclusion: Our data clearly show that PIAS3-mediated feedback loops control cell proliferation and function as robust driving forces for CAC progression. Targeting these highly activated feedback loops might offer promising therapeutic strategies for CAC. Ivyspring International Publisher 2018-04-30 /pmc/articles/PMC5996365/ /pubmed/29896300 http://dx.doi.org/10.7150/thno.23046 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Ma, Junting
Yang, Yaping
Fu, Yong
Guo, Feilong
Zhang, Xiaoyi
Xiao, Shuke
Zhu, Weiming
Huang, Zhen
Zhang, Junfeng
Chen, Jiangning
PIAS3-mediated feedback loops promote chronic colitis-associated malignant transformation
title PIAS3-mediated feedback loops promote chronic colitis-associated malignant transformation
title_full PIAS3-mediated feedback loops promote chronic colitis-associated malignant transformation
title_fullStr PIAS3-mediated feedback loops promote chronic colitis-associated malignant transformation
title_full_unstemmed PIAS3-mediated feedback loops promote chronic colitis-associated malignant transformation
title_short PIAS3-mediated feedback loops promote chronic colitis-associated malignant transformation
title_sort pias3-mediated feedback loops promote chronic colitis-associated malignant transformation
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996365/
https://www.ncbi.nlm.nih.gov/pubmed/29896300
http://dx.doi.org/10.7150/thno.23046
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