He Dabao, Yang Xiaoling, Kuang Wenbin, Huang Guoqing, Liu Xiaohong, Zhang Yonggang
Department of Laboratory Medicine, Shenzhen Longhua District Central Hospital, Shenzhen 518110, People's Republic of China.
Department of Laboratory Medicine, Shenzhen Baoan District Songgang People's Hospital, Shenzhen 518105, People's Republic of China.
Onco Targets Ther. 2020 Oct 9;13:10149-10159. doi: 10.2147/OTT.S274574. eCollection 2020.
Triple negative breast cancer (TNBC), a special subtype of breast cancer, is characterized by high recurrence, mortality and few treatments. To date, the key factors contributing to TNBC progression have not been fully identified. In the current study, we found a TNBC-related circular RNA (circRNA), circ-PGAP3, and explored its biological function, clinical significance and potential mechanism of action.
The functional assay was carried out using CCK-8, colony formation and Transwell invasion assays. RIP, RNA pull-down and luciferase reporter assays were used to test the correlation between circ-PGAP3, miR-330-3p and Myc. The animal model was employed to verify the function of circ-PGAP3 in vivo.
Circ-PGAP3 expression was significantly increased in TNBC tissues. High circ-PGAP3 was closely associated with large tumor size, lymph node metastasis, later TNM stage and dismal outcome. Through performing a series of in vitro and in vivo experiments, we found that circ-PGAP3 promoted TNBC cell growth and metastasis via sponging and inhibiting miR-330-3p, resulting in the upregulation of proto-oncogene Myc. Importantly, circ-PGAP3 expression was positively correlated with the Myc protein level but negatively correlated with miR-330-3p expression in TNBC tissues. Moreover, silencing of miR-330-3p or overexpression of Myc could effectively rescue the weakened malignant phenotype induced by circ-PGAP3 knockdown.
Our results unveil the important driving role of circ-PGAP3 in TNBC development and progression, which provides a candidate therapeutic target for TNBC patients.
三阴性乳腺癌(TNBC)是乳腺癌的一种特殊亚型,具有高复发率、高死亡率且治疗手段有限的特点。迄今为止,导致TNBC进展的关键因素尚未完全明确。在本研究中,我们发现了一种与TNBC相关的环状RNA(circRNA),即circ-PGAP3,并探讨了其生物学功能、临床意义及潜在作用机制。
采用CCK-8、集落形成和Transwell侵袭实验进行功能分析。运用RIP、RNA下拉和荧光素酶报告基因实验检测circ-PGAP3、miR-330-3p和Myc之间的相关性。利用动物模型在体内验证circ-PGAP3的功能。
circ-PGAP3在TNBC组织中的表达显著增加。高表达的circ-PGAP3与肿瘤体积大、淋巴结转移、TNM分期晚及预后不良密切相关。通过一系列体外和体内实验,我们发现circ-PGAP3通过海绵吸附和抑制miR-330-3p促进TNBC细胞生长和转移,导致原癌基因Myc上调。重要的是,在TNBC组织中,circ-PGAP3表达与Myc蛋白水平呈正相关,与miR-330-3p表达呈负相关。此外,沉默miR-330-3p或过表达Myc可有效挽救circ-PGAP3敲低诱导的恶性表型减弱。
我们的研究结果揭示了circ-PGAP3在TNBC发生发展中的重要驱动作用,为TNBC患者提供了一个潜在的治疗靶点。