FOXR2 Interacts with MYC to Promote Its Transcriptional Activities and Tumorigenesis
By combining the results of a large-scale proteomic analysis of the human transcription factor interaction network with knowledge databases, we identified FOXR2 as one of the top-ranked candidate proto-oncogenes. Here, we show that FOXR2 forms a stable complex with MYC and MAX and subsequently regul...
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doaj-1a689b68b64b4b6087d06519b60f08612020-11-25T01:37:53ZengElsevierCell Reports2211-12472016-07-0116248749710.1016/j.celrep.2016.06.004FOXR2 Interacts with MYC to Promote Its Transcriptional Activities and TumorigenesisXu Li0Wenqi Wang1Yuanxin Xi2Min Gao3MyKim Tran4Kathryn E. Aziz5Jun Qin6Wei Li7Junjie Chen8Department of Experimental Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USADepartment of Experimental Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USADepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USADepartment of Experimental Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USADepartment of Experimental Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USADepartment of Experimental Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USADepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USADepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USADepartment of Experimental Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USABy combining the results of a large-scale proteomic analysis of the human transcription factor interaction network with knowledge databases, we identified FOXR2 as one of the top-ranked candidate proto-oncogenes. Here, we show that FOXR2 forms a stable complex with MYC and MAX and subsequently regulates cell proliferation by promoting MYC’s transcriptional activities. We demonstrate that FOXR2 is highly expressed in several breast, lung, and liver cancer cell lines and related patient tumor samples, while reduction of FOXR2 expression in a xenograft model inhibits tumor growth. These results indicate that FOXR2 acts with MYC to promote cancer cell proliferation, which is a potential tumor-specific target for therapeutic intervention against MYC-driven cancers.http://www.sciencedirect.com/science/article/pii/S2211124716307239forkhead boxFOXR2MYCprotein-protein interaction |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xu Li Wenqi Wang Yuanxin Xi Min Gao MyKim Tran Kathryn E. Aziz Jun Qin Wei Li Junjie Chen |
spellingShingle |
Xu Li Wenqi Wang Yuanxin Xi Min Gao MyKim Tran Kathryn E. Aziz Jun Qin Wei Li Junjie Chen FOXR2 Interacts with MYC to Promote Its Transcriptional Activities and Tumorigenesis Cell Reports forkhead box FOXR2 MYC protein-protein interaction |
author_facet |
Xu Li Wenqi Wang Yuanxin Xi Min Gao MyKim Tran Kathryn E. Aziz Jun Qin Wei Li Junjie Chen |
author_sort |
Xu Li |
title |
FOXR2 Interacts with MYC to Promote Its Transcriptional Activities and Tumorigenesis |
title_short |
FOXR2 Interacts with MYC to Promote Its Transcriptional Activities and Tumorigenesis |
title_full |
FOXR2 Interacts with MYC to Promote Its Transcriptional Activities and Tumorigenesis |
title_fullStr |
FOXR2 Interacts with MYC to Promote Its Transcriptional Activities and Tumorigenesis |
title_full_unstemmed |
FOXR2 Interacts with MYC to Promote Its Transcriptional Activities and Tumorigenesis |
title_sort |
foxr2 interacts with myc to promote its transcriptional activities and tumorigenesis |
publisher |
Elsevier |
series |
Cell Reports |
issn |
2211-1247 |
publishDate |
2016-07-01 |
description |
By combining the results of a large-scale proteomic analysis of the human transcription factor interaction network with knowledge databases, we identified FOXR2 as one of the top-ranked candidate proto-oncogenes. Here, we show that FOXR2 forms a stable complex with MYC and MAX and subsequently regulates cell proliferation by promoting MYC’s transcriptional activities. We demonstrate that FOXR2 is highly expressed in several breast, lung, and liver cancer cell lines and related patient tumor samples, while reduction of FOXR2 expression in a xenograft model inhibits tumor growth. These results indicate that FOXR2 acts with MYC to promote cancer cell proliferation, which is a potential tumor-specific target for therapeutic intervention against MYC-driven cancers. |
topic |
forkhead box FOXR2 MYC protein-protein interaction |
url |
http://www.sciencedirect.com/science/article/pii/S2211124716307239 |
work_keys_str_mv |
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