TGF-beta receptor mediated telomerase inhibition, telomere shortening and breast cancer cell senescence.
10.1007/s13238-016-0322-1
- Author:
Lucy CASSAR
1
;
Craig NICHOLLS
1
;
Alex R PINTO
1
;
Ruping CHEN
2
;
Lihui WANG
2
;
He LI
1
;
Jun-Ping LIU
3
Author Information
1. Molecular Signaling Laboratory, Department of Immunology, Central Eastern Clinical School, Monash University, Prahran, VIC, 3181, Australia.
2. Institute of Aging Research, Hangzhou Normal University School of Medicine, Hangzhou, 311121, Zhejiang Province, China.
3. Molecular Signaling Laboratory, Department of Immunology, Central Eastern Clinical School, Monash University, Prahran, VIC, 3181, Australia. jun-ping.liu@monash.edu.
- Publication Type:Journal Article
- Keywords:
BMPRII;
TGFbeta;
breast cancer cells;
hTERT;
senescence;
telomerase;
telomeres
- MeSH:
Actin-Related Protein 2;
genetics;
metabolism;
Activin Receptors, Type II;
genetics;
metabolism;
Bone Morphogenetic Protein 7;
genetics;
metabolism;
Bone Morphogenetic Protein Receptors, Type II;
genetics;
metabolism;
Breast Neoplasms;
genetics;
metabolism;
Cellular Senescence;
Female;
HeLa Cells;
Humans;
MCF-7 Cells;
Neoplasm Proteins;
genetics;
metabolism;
Protein-Serine-Threonine Kinases;
genetics;
metabolism;
Receptor, Transforming Growth Factor-beta Type II;
Receptors, Transforming Growth Factor beta;
genetics;
metabolism;
Smad3 Protein;
genetics;
metabolism;
Telomerase;
genetics;
metabolism;
Telomere Homeostasis
- From:
Protein & Cell
2017;8(1):39-54
- CountryChina
- Language:English
-
Abstract:
Human telomerase reverse transcriptase (hTERT) plays a central role in telomere lengthening for continuous cell proliferation, but it remains unclear how extracellular cues regulate telomerase lengthening of telomeres. Here we report that the cytokine bone morphogenetic protein-7 (BMP7) induces the hTERT gene repression in a BMPRII receptor- and Smad3-dependent manner in human breast cancer cells. Chonic exposure of human breast cancer cells to BMP7 results in short telomeres, cell senescence and apoptosis. Mutation of the BMPRII receptor, but not TGFbRII, ACTRIIA or ACTRIIB receptor, inhibits BMP7-induced repression of the hTERT gene promoter activity, leading to increased telomerase activity, lengthened telomeres and continued cell proliferation. Expression of hTERT prevents BMP7-induced breast cancer cell senescence and apoptosis. Thus, our data suggest that BMP7 induces breast cancer cell aging by a mechanism involving BMPRII receptor- and Smad3-mediated repression of the hTERT gene.
