Insulin-like growth factor binding protein-3 induces senescence by inhibiting telomerase activity in MCF-7 breast cancer cells

被引:3
|
作者
Kwon, Ahreum [1 ]
Chae, Hyun Wook [1 ]
Lee, Woo Jung [1 ]
Kim, JungHyun [1 ]
Kim, Ye Jin [1 ]
Ahn, Jungmin [1 ]
Oh, Youngman [2 ]
Kim, Ho-Seong [1 ,3 ]
机构
[1] Yonsei Univ, Severance Childrens Hosp, Endocrine Res Inst, Coll Med,Dept Pediat, Seoul 03722, South Korea
[2] Virginia Commonwealth Univ, Sch Med, Dept Pathol, Richmond, VA 23298 USA
[3] Yonsei Univ, Endocrine Res Inst, Coll Med, Dept Pediat, 50-1 Yonsei Ro, Seoul 03722, South Korea
关键词
CELLULAR SENESCENCE; IGFBP-3; APOPTOSIS; DEATH; DIFFERENTIATION; FIBROBLASTS; EXPRESSION; CULTURE; ARREST; GENE;
D O I
10.1038/s41598-023-35291-5
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
Insulin-like growth factor binding protein-3 (IGFBP-3) has been known to inhibit cell proliferation and exert tumor-suppressing effects depending on the cell type. In this study, we aimed to show that IGFBP-3 induces cellular senescence via suppression of the telomerase activity, thereby inhibiting MCF-7 breast cancer cell proliferation. We found that the induction of IGFBP-3 in MCF-7 cells enhanced the loss of cell viability. Flow cytometry revealed a higher percentage of non-cycling cells among IGFBP-3-expressing cells than among controls. IGFBP-3 induction also resulted in morphological alterations, such as a flattened cytoplasm and increased granularity, suggesting that IGFBP-3 induces a senescence-like phenotype. The percentage of IGFBP-3 expressing cells with senescence-associated beta-galactosidase activity was 3.4 times higher than control cells. Telomeric repeat amplification and real-time PCR showed that IGFBP-3 decreased telomerase activity by reducing the levels of the RNA component (hTR) and catalytic protein component with reverse transcriptase activity (hTERT) of telomerase in a dose-dependent manner. These results suggest that IGFBP-3 is a negative regulator of MCF-7 breast cancer cell growth by inducing senescence through telomerase suppression.
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页数:13
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