HnRNP-F regulates EMT in bladder cancer by mediating the stabilization of Snail1 mRNA by binding to its 3′ UTRResearch in context

Background: Heterogeneous nuclear ribonucleoprotein F (hnRNP-F) has been implicated in multiple cancers, suggesting its role in tumourigenesis, but the potential oncogenic role and mechanism of hnRNP-F in bladder cancer (BC) remain incompletely understood. Methods: HnRNP-F was identified by proteomi...

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Main Authors: Fei Li, Hongfan Zhao, Mingqiang Su, Weiwei Xie, Yunze Fang, Yuejun Du, Zhe Yu, Lina Hou, Wanlong Tan
Format: Article
Language:English
Published: Elsevier 2019-07-01
Series:EBioMedicine
Online Access:http://www.sciencedirect.com/science/article/pii/S2352396419303986
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author Fei Li
Hongfan Zhao
Mingqiang Su
Weiwei Xie
Yunze Fang
Yuejun Du
Zhe Yu
Lina Hou
Wanlong Tan
author_facet Fei Li
Hongfan Zhao
Mingqiang Su
Weiwei Xie
Yunze Fang
Yuejun Du
Zhe Yu
Lina Hou
Wanlong Tan
author_sort Fei Li
collection DOAJ
description Background: Heterogeneous nuclear ribonucleoprotein F (hnRNP-F) has been implicated in multiple cancers, suggesting its role in tumourigenesis, but the potential oncogenic role and mechanism of hnRNP-F in bladder cancer (BC) remain incompletely understood. Methods: HnRNP-F was identified by proteomic methods. A correlation of hnRNP-F expression with prognosis was analysed in 103 BC patients. Then, we applied in vitro and in vivo methods to reveal the behaviours of hnRNP-F in BC tumourigenesis. Furthermore, the interaction between hnRNP-F and Snail1 mRNA was examined by RNA immunoprecipitation (RIP), and Snail1 mRNA stability was measured after treatment with actinomycin D. Finally, the binding domain between hnRNP-F and Snail1 mRNA was verified by constructing Snail1 mRNA truncations and mutants. Finding: HnRNP-F is significantly upregulated in BC tissue, and its increased expression is associated with a poor prognosis in BC patients. HnRNP-F is necessary for tumour growth, inducing epithelial-mesenchymal transition (EMT) and metastasis in BC. The changes in Snail1 expression were positively correlated with hnRNP-F at both the mRNA and protein levels when hnRNP-F was silenced or enhanced, suggesting that Snail1 is likely a downstream target of hnRNP-F that mediates its effects on enhancing invasion, metastasis and EMT in BC. The overexpression of hnRNP-F caused an increase in the stability of Snail1 mRNA. Our RNA chip analysis revealed that hnRNP-F could combine with Snail1 mRNA, and we further demonstrated that hnRNP-F could directly bind to the 3′ untranslated region (3′ UTR) of Snail1 mRNA to enhance its stability. Interpretation: Our findings suggest that hnRNP-F mediates the stabilization of Snail1 mRNA by binding to its 3′ UTR, subsequently regulating EMT. Keywords: Bladder cancer, Heterogeneous nuclear ribonucleoprotein F, Snail1, Stabilization, Epithelial-mesenchymal transition
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spelling doaj.art-e53056d367d043b29fe9aace8db02ab52022-12-21T19:55:34ZengElsevierEBioMedicine2352-39642019-07-0145208219HnRNP-F regulates EMT in bladder cancer by mediating the stabilization of Snail1 mRNA by binding to its 3′ UTRResearch in contextFei Li0Hongfan Zhao1Mingqiang Su2Weiwei Xie3Yunze Fang4Yuejun Du5Zhe Yu6Lina Hou7Wanlong Tan8Department of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, PR ChinaDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, PR ChinaDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, PR ChinaDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, PR ChinaDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, PR ChinaDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, PR ChinaDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, PR China; Correspondence to: Z. Yu, Department of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, PR China.Department of Healthy Management, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, PR China; Correspondence to: L. Hou, Department of Healthy Management, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, PR China.Department of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, PR China; Correspondence to: W. Tan, Department of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, PR China.Background: Heterogeneous nuclear ribonucleoprotein F (hnRNP-F) has been implicated in multiple cancers, suggesting its role in tumourigenesis, but the potential oncogenic role and mechanism of hnRNP-F in bladder cancer (BC) remain incompletely understood. Methods: HnRNP-F was identified by proteomic methods. A correlation of hnRNP-F expression with prognosis was analysed in 103 BC patients. Then, we applied in vitro and in vivo methods to reveal the behaviours of hnRNP-F in BC tumourigenesis. Furthermore, the interaction between hnRNP-F and Snail1 mRNA was examined by RNA immunoprecipitation (RIP), and Snail1 mRNA stability was measured after treatment with actinomycin D. Finally, the binding domain between hnRNP-F and Snail1 mRNA was verified by constructing Snail1 mRNA truncations and mutants. Finding: HnRNP-F is significantly upregulated in BC tissue, and its increased expression is associated with a poor prognosis in BC patients. HnRNP-F is necessary for tumour growth, inducing epithelial-mesenchymal transition (EMT) and metastasis in BC. The changes in Snail1 expression were positively correlated with hnRNP-F at both the mRNA and protein levels when hnRNP-F was silenced or enhanced, suggesting that Snail1 is likely a downstream target of hnRNP-F that mediates its effects on enhancing invasion, metastasis and EMT in BC. The overexpression of hnRNP-F caused an increase in the stability of Snail1 mRNA. Our RNA chip analysis revealed that hnRNP-F could combine with Snail1 mRNA, and we further demonstrated that hnRNP-F could directly bind to the 3′ untranslated region (3′ UTR) of Snail1 mRNA to enhance its stability. Interpretation: Our findings suggest that hnRNP-F mediates the stabilization of Snail1 mRNA by binding to its 3′ UTR, subsequently regulating EMT. Keywords: Bladder cancer, Heterogeneous nuclear ribonucleoprotein F, Snail1, Stabilization, Epithelial-mesenchymal transitionhttp://www.sciencedirect.com/science/article/pii/S2352396419303986
spellingShingle Fei Li
Hongfan Zhao
Mingqiang Su
Weiwei Xie
Yunze Fang
Yuejun Du
Zhe Yu
Lina Hou
Wanlong Tan
HnRNP-F regulates EMT in bladder cancer by mediating the stabilization of Snail1 mRNA by binding to its 3′ UTRResearch in context
EBioMedicine
title HnRNP-F regulates EMT in bladder cancer by mediating the stabilization of Snail1 mRNA by binding to its 3′ UTRResearch in context
title_full HnRNP-F regulates EMT in bladder cancer by mediating the stabilization of Snail1 mRNA by binding to its 3′ UTRResearch in context
title_fullStr HnRNP-F regulates EMT in bladder cancer by mediating the stabilization of Snail1 mRNA by binding to its 3′ UTRResearch in context
title_full_unstemmed HnRNP-F regulates EMT in bladder cancer by mediating the stabilization of Snail1 mRNA by binding to its 3′ UTRResearch in context
title_short HnRNP-F regulates EMT in bladder cancer by mediating the stabilization of Snail1 mRNA by binding to its 3′ UTRResearch in context
title_sort hnrnp f regulates emt in bladder cancer by mediating the stabilization of snail1 mrna by binding to its 3 utrresearch in context
url http://www.sciencedirect.com/science/article/pii/S2352396419303986
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