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BRCA1-IRIS promotes human tumor progression through PTEN blockade and HIF-1α activation
BRCA1 is an established breast and ovarian tumor suppressor gene that encodes multiple protein products whose individual contributions to human cancer suppression are poorly understood. BRCA1-IRIS (also known as “IRIS”), an alternatively spliced BRCA1 product and a chromatin-bound replication and tr...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6187201/ https://www.ncbi.nlm.nih.gov/pubmed/30254159 http://dx.doi.org/10.1073/pnas.1807112115 |
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author | Li, Andrew G. Murphy, Elizabeth C. Culhane, Aedin C. Powell, Emily Wang, Hua Bronson, Roderick T. Von, Thanh Giobbie-Hurder, Anita Gelman, Rebecca S. Briggs, Kimberly J. Piwnica-Worms, Helen Zhao, Jean J. Kung, Andrew L. Kaelin, William G. Livingston, David M. |
author_facet | Li, Andrew G. Murphy, Elizabeth C. Culhane, Aedin C. Powell, Emily Wang, Hua Bronson, Roderick T. Von, Thanh Giobbie-Hurder, Anita Gelman, Rebecca S. Briggs, Kimberly J. Piwnica-Worms, Helen Zhao, Jean J. Kung, Andrew L. Kaelin, William G. Livingston, David M. |
author_sort | Li, Andrew G. |
collection | PubMed |
description | BRCA1 is an established breast and ovarian tumor suppressor gene that encodes multiple protein products whose individual contributions to human cancer suppression are poorly understood. BRCA1-IRIS (also known as “IRIS”), an alternatively spliced BRCA1 product and a chromatin-bound replication and transcription regulator, is overexpressed in various primary human cancers, including breast cancer, lung cancer, acute myeloid leukemia, and certain other carcinomas. Its naturally occurring overexpression can promote the metastasis of patient-derived xenograft (PDX) cells and other human cancer cells in mouse models. The IRIS-driven metastatic mechanism results from IRIS-dependent suppression of phosphatase and tensin homolog (PTEN) transcription, which in turn perturbs the PI3K/AKT/GSK-3β pathway leading to prolyl hydroxylase-independent HIF-1α stabilization and activation in a normoxic environment. Thus, despite the tumor-suppressing genetic origin of IRIS, its properties more closely resemble those of an oncoprotein that, when spontaneously overexpressed, can, paradoxically, drive human tumor progression. |
format | Online Article Text |
id | pubmed-6187201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-61872012018-10-15 BRCA1-IRIS promotes human tumor progression through PTEN blockade and HIF-1α activation Li, Andrew G. Murphy, Elizabeth C. Culhane, Aedin C. Powell, Emily Wang, Hua Bronson, Roderick T. Von, Thanh Giobbie-Hurder, Anita Gelman, Rebecca S. Briggs, Kimberly J. Piwnica-Worms, Helen Zhao, Jean J. Kung, Andrew L. Kaelin, William G. Livingston, David M. Proc Natl Acad Sci U S A PNAS Plus BRCA1 is an established breast and ovarian tumor suppressor gene that encodes multiple protein products whose individual contributions to human cancer suppression are poorly understood. BRCA1-IRIS (also known as “IRIS”), an alternatively spliced BRCA1 product and a chromatin-bound replication and transcription regulator, is overexpressed in various primary human cancers, including breast cancer, lung cancer, acute myeloid leukemia, and certain other carcinomas. Its naturally occurring overexpression can promote the metastasis of patient-derived xenograft (PDX) cells and other human cancer cells in mouse models. The IRIS-driven metastatic mechanism results from IRIS-dependent suppression of phosphatase and tensin homolog (PTEN) transcription, which in turn perturbs the PI3K/AKT/GSK-3β pathway leading to prolyl hydroxylase-independent HIF-1α stabilization and activation in a normoxic environment. Thus, despite the tumor-suppressing genetic origin of IRIS, its properties more closely resemble those of an oncoprotein that, when spontaneously overexpressed, can, paradoxically, drive human tumor progression. National Academy of Sciences 2018-10-09 2018-09-25 /pmc/articles/PMC6187201/ /pubmed/30254159 http://dx.doi.org/10.1073/pnas.1807112115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | PNAS Plus Li, Andrew G. Murphy, Elizabeth C. Culhane, Aedin C. Powell, Emily Wang, Hua Bronson, Roderick T. Von, Thanh Giobbie-Hurder, Anita Gelman, Rebecca S. Briggs, Kimberly J. Piwnica-Worms, Helen Zhao, Jean J. Kung, Andrew L. Kaelin, William G. Livingston, David M. BRCA1-IRIS promotes human tumor progression through PTEN blockade and HIF-1α activation |
title | BRCA1-IRIS promotes human tumor progression through PTEN blockade and HIF-1α activation |
title_full | BRCA1-IRIS promotes human tumor progression through PTEN blockade and HIF-1α activation |
title_fullStr | BRCA1-IRIS promotes human tumor progression through PTEN blockade and HIF-1α activation |
title_full_unstemmed | BRCA1-IRIS promotes human tumor progression through PTEN blockade and HIF-1α activation |
title_short | BRCA1-IRIS promotes human tumor progression through PTEN blockade and HIF-1α activation |
title_sort | brca1-iris promotes human tumor progression through pten blockade and hif-1α activation |
topic | PNAS Plus |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6187201/ https://www.ncbi.nlm.nih.gov/pubmed/30254159 http://dx.doi.org/10.1073/pnas.1807112115 |
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