LncRNA LINC01857 reduces metastasis and angiogenesis in breast cancer cells via regulating miR-2052/CENPQ axis

Author:

Qian Weiwei1,Yang Linlin2,Ni Yi1,Yin Fei1,Qin Lili3,Yang Yang4

Affiliation:

1. Department of Breast Surgery, Nantong Third People’s Hospital, Nantong University , Nantong , Jiangsu Province , China

2. Department of Oncology, Sheyang People’s Hospital , Yancheng City , Jiangsu Province 224300 , China

3. Department of Endoscopic Center, Affiliated Hospital of Nantong University , Nantong City , Jiangsu Province 226001 , China

4. Department of Trauma Center, Affiliated Hospital of Nantong University , No. 20 Xisi Road, Chongchuan District , Nantong City , Jiangsu Province 226001 , China

Abstract

Abstract Long non-coding RNAs have been confirmed closely related to the metastasis and angiogenesis of breast cancer (BC). LINC01857 can promote the growth and metastasis of BC cells. The present work focused on exploring the role of LINC01857 in BC metastasis and angiogenesis and investigating the possible mechanisms. The results showed that LINC01857 and CENPQ were highly expressed in BC tissues and cells, while miR-2052 was contrarily expressed. In vitro study showed that low expression of linc01857 could inhibit the migration ability and vascularization of BC cells, and mir-2052 inhibitor partially restored the effect of si-LINC01857 on the migration ability and vascularization of BC cells. Likewise, inhibition of CENPQ can partially rescue the effects of miR-2052 inhibitor on the migration ability and vascularization of BC cells. In vivo studies showed that down-regulation of LINC01857 notably suppressed tumor growth and angiogenesis in nude mice. The miR-2052 inhibitor partially restored the effects of si-LINC01857. CENPQ suppression partially rescued the effects of the miR-2052 inhibitor. To conclude, LINC01857/miR-2052/CENPQ is the potential novel target for BC treatment.

Publisher

Walter de Gruyter GmbH

Subject

General Medicine

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