BRCA1-IRIS promotes human tumor progression through PTEN blockade and HIF-1α activation

被引:21
作者
Li, Andrew G. [1 ,2 ]
Murphy, Elizabeth C. [2 ]
Culhane, Aedin C. [3 ,4 ]
Powell, Emily [5 ]
Wang, Hua [1 ,2 ]
Bronson, Roderick T. [6 ]
Thanh Von [2 ,7 ]
Giobbie-Hurder, Anita [3 ]
Gelman, Rebecca S. [3 ,4 ]
Briggs, Kimberly J. [8 ]
Piwnica-Worms, Helen [5 ]
Zhao, Jean J. [2 ,7 ]
Kung, Andrew L. [9 ]
Kaelin, William G., Jr. [8 ,10 ]
Livingston, David M. [1 ,2 ]
机构
[1] Harvard Med Sch, Dept Genet, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02215 USA
[3] Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02215 USA
[4] Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX 77030 USA
[6] Harvard Med Sch, Dept Pathol, Boston, MA 02115 USA
[7] Harvard Med Sch, Dept Biol Chem & Mol Pharmacol, Boston, MA 02215 USA
[8] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02215 USA
[9] Mem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10065 USA
[10] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
关键词
BRCA1-IRIS; metastasis; HIF-1; alpha; PTEN; HYPOXIA-INDUCIBLE FACTORS; EPITHELIAL-MESENCHYMAL TRANSITION; PROTEIN-KINASE; FACTOR; 1-ALPHA; BREAST-CANCER; PHOSPHATASE-ACTIVITY; CELL-SURVIVAL; HIF-ALPHA; NUDE-MICE; EXPRESSION;
D O I
10.1073/pnas.1807112115
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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-3 beta pathway leading to prolyl hydroxylase-independent HIF-1 alpha 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.
引用
收藏
页码:E9600 / E9609
页数:10
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