Department Of Pathology, Dongying People's Hospital, Dongying City, Shandong Province, China.
Department Of Radiology, Dongying People's Hospital, Dongying City, Shandong Province, China.
Bioengineered. 2021 Dec;12(1):5850-5858. doi: 10.1080/21655979.2021.1964155.
Breast cancer has been known as cancer with high mortality rates. It has been studied that MEX3A (Mex-3 RNA Binding Family Member A) is involved in carcinogenesis by accelerating cancer proliferation and migration. Therefore, this research aimed to study how MEX3A regulates the biological behaviors of breast cancer. Firstly, we used GEPIA and KM-plotter databases to evaluate MEX3A expression in human breast cancer tissue compared to adjacent normal tissue. Immunohistochemistry was employed to assess MEX3A protein expression in clinical specimens. MEX3A mRNA expression level was assessed through quantitative real-time PCR (RT-qPCR). Western blotting was used to detect protein expression. Moreover, Cell Count Kit-8 (CCK-8) assay, wound healing assay and transwell invasion assay were used to determine the proliferation, migration and invasion of breast cancer cells, respectively. Our study found that MEX3A expression level was much higher in human breast cancer tissues as compared to adjacent normal tissues. Similarly, breast cancer cell lines showed higher expression of MEX3A as compared to the normal breast cells. This higher expression of MEX3A was linked with the poor survival of breast cancer. Moreover, we found that overexpression of MEX3A stimulated proliferation and migration in the breast cancer cells. However, inhibition of MEX3A significantly reduced the proliferation and migration of breast cancer cells. In addition, we determined that MEX3A could activate RhoA/ROCK1/LIMK1 signaling in the breast cancer cells. Overall, our study concluded that MEX3A promotes its migration and proliferation in breast cancer cells via modulating RhoA/ROCK1/LIMK1 signaling pathway.
乳腺癌一直以来被认为是死亡率较高的癌症。有研究表明,MEX3A(Mex-3 RNA 结合家族成员 A)通过加速癌症增殖和迁移参与致癌作用。因此,本研究旨在研究 MEX3A 如何调节乳腺癌的生物学行为。首先,我们使用 GEPIA 和 KM-plotter 数据库评估了人乳腺癌组织与相邻正常组织相比 MEX3A 的表达。免疫组织化学用于评估临床标本中 MEX3A 蛋白的表达。通过定量实时 PCR(RT-qPCR)评估 MEX3A mRNA 表达水平。Western blot 用于检测蛋白表达。此外,细胞计数试剂盒-8(CCK-8)测定、划痕愈合测定和 Transwell 侵袭测定分别用于测定乳腺癌细胞的增殖、迁移和侵袭。我们的研究发现,与相邻正常组织相比,人乳腺癌组织中 MEX3A 的表达水平要高得多。同样,乳腺癌细胞系的 MEX3A 表达水平也高于正常乳腺细胞。这种 MEX3A 的高表达与乳腺癌的不良预后有关。此外,我们发现 MEX3A 的过表达刺激了乳腺癌细胞的增殖和迁移。然而,MEX3A 的抑制显著降低了乳腺癌细胞的增殖和迁移。此外,我们确定 MEX3A 可以在乳腺癌细胞中激活 RhoA/ROCK1/LIMK1 信号通路。总的来说,我们的研究得出结论,MEX3A 通过调节 RhoA/ROCK1/LIMK1 信号通路促进乳腺癌细胞的迁移和增殖。