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LncRNA HAND2-AS1 suppressed the growth of triple negative breast cancer via reducing secretion of MSCs derived exosomal miR-106a-5p

Xing LiDepartment of Obstetrics and Gynecology, Shanghai Eighth People Hospital, Xuhui, Shanghai, ChinaXiaolong TangDepartment of General Surgery, Shanghai Eighth People Hospital, Xuhui, Shanghai, ChinaKaikai WuDepartment of General Surgery, Shanghai Eighth People Hospital, Xuhui, Shanghai, ChinaXiong HuangDepartment of General Surgery, Shanghai Eighth People Hospital, Xuhui, Shanghai, ChinaYi YiDepartment of General Surgery, Shanghai Eighth People Hospital, Xuhui, Shanghai, ChinaJinliang HuanDepartment of General Surgery, Shanghai Eighth People Hospital, Xuhui, Shanghai, China
2020en
ABI

Аннотация

BACKGROUND: Triple-negative breast cancer (TNBC) is a special type of breast cancer, its tumor cell metastasis rate is much higher than other types, and at the same time has a high rate of postoperative recurrence, which significantly threatens the health of women. Thus, it is urgent to explore a new treatment for TNBC. RESULTS: MiR-106a-5p was up-regulated in TNBC tissues and cells, and was positively correlated with the tumor grade, which indicated poor prognosis in TNBC patients. Mesenchymal stem cells (MSCs) can transport miR-106a-5p into TNBC cells via exosomes. Functional analysis showed exo-miR-106a-5p secreted by MSCs promoted tumor progression in TNBC cells. Furthermore, lncRNA HAND2-AS1 inhibited miR-106a-5p levels, and HAND2-AS1 was decreased in TNBC tissues and cells. Besides, overexpression of HAND2-AS1 reduced the secretion of exo-miR-106a-5p secretion from MSCs, thus suppressed TNBC development. CONCLUSION: Our study revealed that HAND2-AS1 inhibited the growth of TNBC, which were mediated by the inhibitory effects of MSC-derived exosomal miR-106a-5p.

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