Liang Yingxiu, Li Chunyang, Hou Xiaohong, Lin Yiguang, Cheng Jing
Reproductive Center, Department of Obstetrics and Gynecology, The Second Affiliated Hospital and the Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Department of Biochemistry, School of Basic Sciences, Wenzhou Medical University, Wenzhou, China.
Front Oncol. 2024 May 10;14:1361721. doi: 10.3389/fonc.2024.1361721. eCollection 2024.
MicroRNA-875-5p (miR-875-5p) is a cancer-related microRNA. It has been demonstrated that miR-875-5p participates in the development of various types of cancer such as hepatocellular carcinoma, gastric carcinoma, prostate and bladder cancer. Previous research suggested that miR-875 is implicated in the development of cervical cancer cells. However, the exact role and function of miR-875-5p in cervical cancer remain unexplored. It is important to examine the role and function of miR-875-5p and the associated signaling pathway, as the findings may have diagnostic and therapeutic significance. Thus, in this study, we investigated the effect of miR-875-5p on the growth and metastasis of cervical cancer cells and the possible underlying mechanisms.
Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was used to detect the expression of miR-875-5p in cervical cancer cells and normal cervical epithelium. After overexpression or co-expression of miR-875-5p in cells, the changes in cell function were analyzed. Western blot was used to detect the expression changes of epithelial-mesenchymal transition (EMT) -related proteins and autophagy-related proteins.
Functional studies demonstrated that miR-875-5p overexpression significantly inhibited the proliferation, migration, invasion, and EMT, and promotes apoptosis and autophagy of cervical cancer cells., while miR-875-5p knockdown promoted the proliferation, migration, invasion, and EMT, and inhibited apoptosis and autophagy cervical cancer cells. Furthermore, Western blot results showed that overexpression of miR-875-5p downregulated the expressions of N-cadherin, Snail, Vimentin and microtubule-associated protein 1 light chain 3B I (LC3B I). Conversely, miR-875-5p upregulated the expression of E-cadherin.
In conclusion, our findings suggest that miR-875-5p functions as a tumor inhibitor suppressing the growth and metastasis of cervical cancer. Overexpression of miR-875-5p inhibits malignant behavior and promotes autophagy and apoptosis in cervical cancer cells. These findings advance our understanding of the role and function of miR-875-5p in cervical cancer and could facilitate the development of early genetic markers or biomarkers and therapeutic targets for cervical cancer.
微小RNA - 875 - 5p(miR - 875 - 5p)是一种与癌症相关的微小RNA。已证实miR - 875 - 5p参与多种类型癌症的发展,如肝细胞癌、胃癌、前列腺癌和膀胱癌。先前的研究表明miR - 875与宫颈癌细胞的发展有关。然而,miR - 875 - 5p在宫颈癌中的确切作用和功能仍未得到探索。研究miR - 875 - 5p的作用和功能以及相关信号通路很重要,因为这些发现可能具有诊断和治疗意义。因此,在本研究中,我们研究了miR - 875 - 5p对宫颈癌细胞生长和转移的影响以及可能的潜在机制。
采用逆转录定量聚合酶链反应(RT - qPCR)检测miR - 875 - 5p在宫颈癌细胞和正常宫颈上皮中的表达。在细胞中过表达或共表达miR - 875 - 5p后,分析细胞功能的变化。蛋白质免疫印迹法用于检测上皮 - 间质转化(EMT)相关蛋白和自噬相关蛋白的表达变化。
功能研究表明,miR - 875 - 5p过表达显著抑制宫颈癌细胞的增殖、迁移、侵袭和EMT,并促进其凋亡和自噬,而敲低miR - 875 - 5p则促进宫颈癌细胞的增殖、迁移、侵袭和EMT,并抑制其凋亡和自噬。此外,蛋白质免疫印迹结果显示,miR - 875 - 5p过表达下调了N - 钙黏蛋白、Snail、波形蛋白和微管相关蛋白1轻链3B I(LC3B I)的表达。相反,miR - 875 - 5p上调了E - 钙黏蛋白的表达。
总之,我们的研究结果表明,miR - 875 - 5p作为一种肿瘤抑制因子,抑制宫颈癌的生长和转移。miR - 875 - 5p过表达抑制宫颈癌细胞的恶性行为并促进其自噬和凋亡。这些发现加深了我们对miR - 875 - 5p在宫颈癌中作用和功能的理解,并可能有助于开发宫颈癌的早期遗传标志物或生物标志物以及治疗靶点。