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A KLF6-driven transcriptional network links lipid homeostasis and tumour growth in renal carcinoma
Transcriptional networks are critical for the establishment of tissue-specific cellular states in health and disease, including cancer. Yet, the transcriptional circuits that control carcinogenesis remain poorly understood. Here we report that Kruppel like factor 6 (KLF6), a transcription factor of...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411998/ https://www.ncbi.nlm.nih.gov/pubmed/30858363 http://dx.doi.org/10.1038/s41467-019-09116-x |
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author | Syafruddin, Saiful E. Rodrigues, Paulo Vojtasova, Erika Patel, Saroor A. Zaini, M. Nazhif Burge, Johanna Warren, Anne Y. Stewart, Grant D. Eisen, Tim Bihary, Dóra Samarajiwa, Shamith A. Vanharanta, Sakari |
author_facet | Syafruddin, Saiful E. Rodrigues, Paulo Vojtasova, Erika Patel, Saroor A. Zaini, M. Nazhif Burge, Johanna Warren, Anne Y. Stewart, Grant D. Eisen, Tim Bihary, Dóra Samarajiwa, Shamith A. Vanharanta, Sakari |
author_sort | Syafruddin, Saiful E. |
collection | PubMed |
description | Transcriptional networks are critical for the establishment of tissue-specific cellular states in health and disease, including cancer. Yet, the transcriptional circuits that control carcinogenesis remain poorly understood. Here we report that Kruppel like factor 6 (KLF6), a transcription factor of the zinc finger family, regulates lipid homeostasis in clear cell renal cell carcinoma (ccRCC). We show that KLF6 supports the expression of lipid metabolism genes and promotes the expression of PDGFB, which activates mTOR signalling and the downstream lipid metabolism regulators SREBF1 and SREBF2. KLF6 expression is driven by a robust super enhancer that integrates signals from multiple pathways, including the ccRCC-initiating VHL-HIF2A pathway. These results suggest an underlying mechanism for high mTOR activity in ccRCC cells. More generally, the link between super enhancer-driven transcriptional networks and essential metabolic pathways may provide clues to the mechanisms that maintain the stability of cell identity-defining transcriptional programmes in cancer. |
format | Online Article Text |
id | pubmed-6411998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64119982019-03-13 A KLF6-driven transcriptional network links lipid homeostasis and tumour growth in renal carcinoma Syafruddin, Saiful E. Rodrigues, Paulo Vojtasova, Erika Patel, Saroor A. Zaini, M. Nazhif Burge, Johanna Warren, Anne Y. Stewart, Grant D. Eisen, Tim Bihary, Dóra Samarajiwa, Shamith A. Vanharanta, Sakari Nat Commun Article Transcriptional networks are critical for the establishment of tissue-specific cellular states in health and disease, including cancer. Yet, the transcriptional circuits that control carcinogenesis remain poorly understood. Here we report that Kruppel like factor 6 (KLF6), a transcription factor of the zinc finger family, regulates lipid homeostasis in clear cell renal cell carcinoma (ccRCC). We show that KLF6 supports the expression of lipid metabolism genes and promotes the expression of PDGFB, which activates mTOR signalling and the downstream lipid metabolism regulators SREBF1 and SREBF2. KLF6 expression is driven by a robust super enhancer that integrates signals from multiple pathways, including the ccRCC-initiating VHL-HIF2A pathway. These results suggest an underlying mechanism for high mTOR activity in ccRCC cells. More generally, the link between super enhancer-driven transcriptional networks and essential metabolic pathways may provide clues to the mechanisms that maintain the stability of cell identity-defining transcriptional programmes in cancer. Nature Publishing Group UK 2019-03-11 /pmc/articles/PMC6411998/ /pubmed/30858363 http://dx.doi.org/10.1038/s41467-019-09116-x Text en © The Author(s) 2019 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 Syafruddin, Saiful E. Rodrigues, Paulo Vojtasova, Erika Patel, Saroor A. Zaini, M. Nazhif Burge, Johanna Warren, Anne Y. Stewart, Grant D. Eisen, Tim Bihary, Dóra Samarajiwa, Shamith A. Vanharanta, Sakari A KLF6-driven transcriptional network links lipid homeostasis and tumour growth in renal carcinoma |
title | A KLF6-driven transcriptional network links lipid homeostasis and tumour growth in renal carcinoma |
title_full | A KLF6-driven transcriptional network links lipid homeostasis and tumour growth in renal carcinoma |
title_fullStr | A KLF6-driven transcriptional network links lipid homeostasis and tumour growth in renal carcinoma |
title_full_unstemmed | A KLF6-driven transcriptional network links lipid homeostasis and tumour growth in renal carcinoma |
title_short | A KLF6-driven transcriptional network links lipid homeostasis and tumour growth in renal carcinoma |
title_sort | klf6-driven transcriptional network links lipid homeostasis and tumour growth in renal carcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411998/ https://www.ncbi.nlm.nih.gov/pubmed/30858363 http://dx.doi.org/10.1038/s41467-019-09116-x |
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