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A feed-forward loop between nuclear translocation of CXCR4 and HIF-1α promotes renal cell carcinoma metastasis

CXC chemokine receptor 4 (CXCR4) has been suggested to play a critical role in cancer metastasis. Some studies have described CXCR4 nuclear localization in metastatic lesions of renal cell carcinoma (RCC), which has been suggested to be correlated with cancer metastasis. However, the underlying mech...

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Autores principales: Bao, Yi, Wang, Zhixiang, Liu, Bing, Lu, Xin, Xiong, Ying, Shi, Jiazi, Li, Peng, Chen, Junming, Zhang, Zongqin, Chen, Ming, Wang, Linhui, Wu, Zhenjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367212/
https://www.ncbi.nlm.nih.gov/pubmed/30177838
http://dx.doi.org/10.1038/s41388-018-0452-4
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author Bao, Yi
Wang, Zhixiang
Liu, Bing
Lu, Xin
Xiong, Ying
Shi, Jiazi
Li, Peng
Chen, Junming
Zhang, Zongqin
Chen, Ming
Wang, Linhui
Wu, Zhenjie
author_facet Bao, Yi
Wang, Zhixiang
Liu, Bing
Lu, Xin
Xiong, Ying
Shi, Jiazi
Li, Peng
Chen, Junming
Zhang, Zongqin
Chen, Ming
Wang, Linhui
Wu, Zhenjie
author_sort Bao, Yi
collection PubMed
description CXC chemokine receptor 4 (CXCR4) has been suggested to play a critical role in cancer metastasis. Some studies have described CXCR4 nuclear localization in metastatic lesions of renal cell carcinoma (RCC), which has been suggested to be correlated with cancer metastasis. However, the underlying mechanism and clinical significance of CXCR4 nuclear localization remains unknown. Here, we show that CXCR4 nuclear localization is more likely to occur in RCC tissues, especially in metastases, and is associated with poor prognosis. CXCR4 nuclear localization requires its nuclear localization sequence (NLS, residues 146-RPRK-149). After the mutation of NLS in CXCR4, CXCR4 nuclear localization in RCC cells is lost. Nuclear localization of CXCR4 promoted RCC tumorigenicity both in vitro and in vivo. Mechanistically, we found that CXCR4 and hypoxia-inducible factor-1α (HIF-1α) colocalized in RCC cells and interacted with each other. Moreover, CXCR4 nuclear localization promoted nuclear accumulation of HIF-1α, thereby promoting the expression of genes downstream of HIF-1α. Reciprocally, nuclear HIF-1α promoted CXCR4 transcription, thus forming a feed-forward loop. Subcellular CXCR4 and HIF-1α expression levels were independent adverse prognostic factors and could be combined with TNM stage to generate a predictive nomogram of the clinical outcome of patients with RCC. Therefore, our findings indicate that CXCR4 nuclear translocation plays a critical role in RCC metastasis and may serve as a prognostic biomarker and potential therapeutic target.
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spelling pubmed-63672122019-02-11 A feed-forward loop between nuclear translocation of CXCR4 and HIF-1α promotes renal cell carcinoma metastasis Bao, Yi Wang, Zhixiang Liu, Bing Lu, Xin Xiong, Ying Shi, Jiazi Li, Peng Chen, Junming Zhang, Zongqin Chen, Ming Wang, Linhui Wu, Zhenjie Oncogene Article CXC chemokine receptor 4 (CXCR4) has been suggested to play a critical role in cancer metastasis. Some studies have described CXCR4 nuclear localization in metastatic lesions of renal cell carcinoma (RCC), which has been suggested to be correlated with cancer metastasis. However, the underlying mechanism and clinical significance of CXCR4 nuclear localization remains unknown. Here, we show that CXCR4 nuclear localization is more likely to occur in RCC tissues, especially in metastases, and is associated with poor prognosis. CXCR4 nuclear localization requires its nuclear localization sequence (NLS, residues 146-RPRK-149). After the mutation of NLS in CXCR4, CXCR4 nuclear localization in RCC cells is lost. Nuclear localization of CXCR4 promoted RCC tumorigenicity both in vitro and in vivo. Mechanistically, we found that CXCR4 and hypoxia-inducible factor-1α (HIF-1α) colocalized in RCC cells and interacted with each other. Moreover, CXCR4 nuclear localization promoted nuclear accumulation of HIF-1α, thereby promoting the expression of genes downstream of HIF-1α. Reciprocally, nuclear HIF-1α promoted CXCR4 transcription, thus forming a feed-forward loop. Subcellular CXCR4 and HIF-1α expression levels were independent adverse prognostic factors and could be combined with TNM stage to generate a predictive nomogram of the clinical outcome of patients with RCC. Therefore, our findings indicate that CXCR4 nuclear translocation plays a critical role in RCC metastasis and may serve as a prognostic biomarker and potential therapeutic target. Nature Publishing Group UK 2018-09-03 2019 /pmc/articles/PMC6367212/ /pubmed/30177838 http://dx.doi.org/10.1038/s41388-018-0452-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bao, Yi
Wang, Zhixiang
Liu, Bing
Lu, Xin
Xiong, Ying
Shi, Jiazi
Li, Peng
Chen, Junming
Zhang, Zongqin
Chen, Ming
Wang, Linhui
Wu, Zhenjie
A feed-forward loop between nuclear translocation of CXCR4 and HIF-1α promotes renal cell carcinoma metastasis
title A feed-forward loop between nuclear translocation of CXCR4 and HIF-1α promotes renal cell carcinoma metastasis
title_full A feed-forward loop between nuclear translocation of CXCR4 and HIF-1α promotes renal cell carcinoma metastasis
title_fullStr A feed-forward loop between nuclear translocation of CXCR4 and HIF-1α promotes renal cell carcinoma metastasis
title_full_unstemmed A feed-forward loop between nuclear translocation of CXCR4 and HIF-1α promotes renal cell carcinoma metastasis
title_short A feed-forward loop between nuclear translocation of CXCR4 and HIF-1α promotes renal cell carcinoma metastasis
title_sort feed-forward loop between nuclear translocation of cxcr4 and hif-1α promotes renal cell carcinoma metastasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367212/
https://www.ncbi.nlm.nih.gov/pubmed/30177838
http://dx.doi.org/10.1038/s41388-018-0452-4
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