Key Laboratory of Birth Defects and Related Diseases of Women and Children, West China Second University Hospital, Sichuan University, Chengdu, 610066, Sichuan, China.
Sichuan Cancer Hospital, No. 55, Section 4, Renmin South Road, Chengdu, 610066, Sichuan, China.
Biochem Genet. 2022 Feb;60(1):153-172. doi: 10.1007/s10528-021-10092-5. Epub 2021 Jun 16.
Ovarian cancer is a common cancer affecting women with high morbidity and mortality globally. Circular RNAs (circRNAs) have been found play vital roles in multifarious cancers, including OC. This study aims to explore the biological role and underlying mechanism of circ_0072995 in OC progression. Circ_0072995 was upregulated in OC tissues and cells in a stable structure. Functional experiments indicated that circ_0072995 knockdown suppressed cell proliferation, migration, invasion and accelerated cell apoptosis of OC cells. Mechanistically, miR-122-5p was a direct target of circ_0072995, and its knockdown reversed the effects of circ_0072995 silence on inhibition of OC cell progression. Meanwhile, SLC1A5 was a downstream target gene of miR-122-5p, and miR-122-5p overexpression inhibited the progression of OC cells by targeting SLC1A5. Moreover, circ_0072995 positively regulated SLC1A5 expression via sponging miR-122-5p. Circ_0072995 could play oncogenic role in tumorigenesis and malignant development of OC by regulating miR-122-5p/SLC1A5 axis, providing a novel approach for OC treatment.
卵巢癌是一种常见的女性癌症,在全球范围内具有较高的发病率和死亡率。环状 RNA(circRNAs)已被发现在多种癌症中发挥重要作用,包括 OC。本研究旨在探讨 circ_0072995 在 OC 进展中的生物学作用和潜在机制。circ_0072995 在 OC 组织和细胞中以稳定的结构上调。功能实验表明,circ_0072995 敲低抑制 OC 细胞的增殖、迁移、侵袭,并加速细胞凋亡。机制上,circ_0072995 是 miR-122-5p 的直接靶标,其敲低逆转了 circ_0072995 沉默对抑制 OC 细胞进展的影响。同时,SLC1A5 是 miR-122-5p 的下游靶基因,miR-122-5p 通过靶向 SLC1A5 抑制 OC 细胞的进展。此外,circ_0072995 通过海绵吸附 miR-122-5p 正向调节 SLC1A5 的表达。circ_0072995 通过调节 miR-122-5p/SLC1A5 轴在 OC 的发生和恶性发展中发挥致癌作用,为 OC 的治疗提供了一种新方法。