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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2018
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.
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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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