The lncRNA BORG Drives Breast Cancer Metastasis and Disease Recurrence

被引:85
作者
Gooding, Alex J. [1 ]
Zhang, Bing [2 ]
Jahanbani, Fereshteh Kenari [2 ]
Gilmore, Hannah L. [3 ,4 ]
Chang, Jenny C. [5 ]
Valadkhan, Saba [2 ]
Schiemann, William P. [1 ]
机构
[1] Case Western Reserve Univ, Case Comprehens Canc Ctr, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Mol Biol & Microbiol, Cleveland, OH 44106 USA
[3] Univ Hosp, Dept Pathol, Case Med Ctr, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Cleveland, OH 44106 USA
[5] Houston Methodist Res Ctr, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
LONG NONCODING RNAS; CARCINOMA; GROWTH; KAP1; SUMOYLATION; PROTEIN; DIRECTS; CELLS; GENE; PHOSPHORYLATION;
D O I
10.1038/s41598-017-12716-6
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
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Long noncoding RNAs (lncRNAs) have emerged as potent regulators of breast cancer development and progression, including the metastatic spread of disease. Through in silico and biological analyses, we identified a novel lncRNA, BMP/OP-Responsive Gene (BORG), whose expression directly correlates with aggressive breast cancer phenotypes, as well as with metastatic competence and disease recurrence in multiple clinical cohorts. Mechanistically, BORG elicits the metastatic outgrowth of latent breast cancer cells by promoting the localization and transcriptional repressive activity of TRIM28, which binds BORG and induces substantial alterations in carcinoma proliferation and survival. Moreover, inhibiting BORG expression in metastatic breast cancer cells impedes their metastatic colonization of the lungs of mice, implying that BORG acts as a novel driver of the genetic and epigenetic alterations that underlie the acquisition of metastatic and recurrent phenotypes by breast cancer cells.
引用
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页数:18
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