Han Songtao, Qin Yajuan, He YuJiao, Li Ming, Ma Jing, Luo Ning, Huo Yishan, Meng Xinling, Liu Yunmei
Clinical laboratory center, Hospital of Traditional Chinese Medicine Affiliated to Xinjiang Medical University, Urumqi, 830011, China.
Clinical Laboratory Center, State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, Tumor Hospital Affiliated to Xinjiang Medical University, Urumqi, 830011, China.
BMC Cancer. 2025 Aug 7;25(1):1279. doi: 10.1186/s12885-025-14600-3.
Cervical cancer is a major challenge facing women's health worldwide. In China, its incidence and mortality rate rank first among female reproductive tract malignancies. SNHG15 has been found and proven to have important functions in many cancers. Related studies have shown that miR-200a-3p plays an important role in tumor development. However, there is little research on how the two are involved in the progression of cervical cancer cells and their potential regulatory systems.
qRT-PCR was used to detect the expression of LncRNA SNHG15 in human cervical immortalized squamous cells (Ect1/E6E7) and human cervical cancer cell lines (SiHa, HeLa, Caski, C-33 A). Cervical cancer HeLa and SiHa cells were used as the research objects and were divided into NC, GV493-negative group, SNHG15-shRNA group, empty vector group, and SNHG15-OERNA group. The expression levels of LncRNA SNHG15 and miR-200a-3p in cells were detected by qRT-PCR. CCK8 was used to detect cell proliferation, cell migration and invasion ability, and dual luciferase activity was used to analyze the targeted binding of LncRNA SNHG15 and miR-200a-3p.
Compared with human cervical immortalized squamous cells (Ect1/E6E7), the expression level of LncRNA SNHG15 in human cervical cancer cell lines SiHa, HeLa and C-33 A was increased(P<0.05). Cervical cancer cells HeLa and SiHa with more significant differences were selected for subsequent studies. Overexpression of LncRNA SNHG15 or low expression of miR-200a-3p promoted cell proliferation, migration and invasion (P < 0.05).
High expression of SNHG15 progression cervical cancer cell proliferation, migration, and invasion by targeting the miR-200a-3p gene.
Trial registration: DRKS, ISRCTNDRKS00035987. Registration on 17 February 2025-Retrospectively registered, https://drks.de/register/de/trial/DRKS00035987.
宫颈癌是全球女性健康面临的重大挑战。在中国,其发病率和死亡率在女性生殖道恶性肿瘤中位居首位。已发现并证实SNHG15在多种癌症中具有重要功能。相关研究表明,miR-200a-3p在肿瘤发展中起重要作用。然而,关于二者如何参与宫颈癌细胞的进展及其潜在调控系统的研究较少。
采用qRT-PCR检测长链非编码RNA SNHG15在人宫颈永生化鳞状细胞(Ect1/E6E7)和人宫颈癌细胞系(SiHa、HeLa、Caski、C-33 A)中的表达。以宫颈癌HeLa和SiHa细胞为研究对象,分为NC组、GV493阴性组、SNHG15-shRNA组、空载体组和SNHG15-OERNA组。采用qRT-PCR检测细胞中长链非编码RNA SNHG15和miR-200a-3p的表达水平。采用CCK8检测细胞增殖、细胞迁移和侵袭能力,采用双荧光素酶活性分析长链非编码RNA SNHG15与miR-200a-3p的靶向结合。
与人宫颈永生化鳞状细胞(Ect1/E6E7)相比,人宫颈癌细胞系SiHa、HeLa及C-33 A中长链非编码RNA SNHG15的表达水平升高(P<0.05)。选择差异更显著的宫颈癌HeLa和SiHa细胞进行后续研究。长链非编码RNA SNHG15的过表达或miR-200a-3p的低表达促进细胞增殖、迁移和侵袭(P<0.05)。
SNHG15的高表达通过靶向miR-200a-3p基因促进宫颈癌细胞增殖、迁移和侵袭。
试验注册:DRKS,ISRCTNDRKS00035987。于2025年2月17日注册——追溯注册,https://drks.de/register/de/trial/DRKS00035987。