Wu Chen, Jiang Jiahui, Ci Chao
Department of Dermatology, The First Affiliated Hospital of Wannan Medical College, No. 2 Zheshan West Road, Wuhu, Anhui, 241001, China.
Heliyon. 2024 Jun 5;10(11):e32485. doi: 10.1016/j.heliyon.2024.e32485. eCollection 2024 Jun 15.
Investigating the effects of MYB proto-oncogene like 2 (MYBL2)-mediated regulation of Cell division cycle associated 8 (CDCA8) expression on the biological activity of cutaneous malignant melanoma cells.
A375 cells with MYBL2 and CDCA8 overexpression and knockdown were evaluated using migration, invasion, and proliferation assays. Besides, cell apoptosis was quantified by flow cytometry. To investigate the tumorigenic effects of MYBL2 knockdown , A375 cells with MYBL2 knockdown were injected in BALB/C nude mice.
The levels of MYBL2 and CDCA8 gene expression were notably elevated in A375 cells in comparison to HaCat cells (P < 0.05). Downregulation of MYBL2 led to a notable reduction in the migratory and invasive capability of A375 cells in vitro (P < 0.001). On the contrary, overexpression of MYBL2 enhanced migration and invasion ability (P < 0.001). There existed a positive correlation between CDCA8 and MYBL2 gene and protein expression levels after overexpression or knockdown of MYBL2 (P < 0.001). In the tumorigenic study, the MYBL2 knockdown group displayed a substantial decrease in tumor volume (P < 0.01) and exhibited decreased CDCA8 expression in tumors in comparison to the control group.
We arrived at such a conclusion that MYBL2 promoted the migration, invasion and proliferation ability of cutaneous malignant melanoma cells by targeted regulation of CDCA8 expression in this study.
研究MYB原癌基因样2(MYBL2)介导的细胞分裂周期相关8(CDCA8)表达调控对皮肤恶性黑色素瘤细胞生物学活性的影响。
使用迁移、侵袭和增殖试验评估过表达和敲低MYBL2及CDCA8的A375细胞。此外,通过流式细胞术对细胞凋亡进行定量分析。为研究敲低MYBL2的致瘤作用,将敲低MYBL2的A375细胞注射到BALB/C裸鼠体内。
与HaCat细胞相比,A375细胞中MYBL2和CDCA8基因表达水平显著升高(P < 0.05)。敲低MYBL2导致A375细胞体外迁移和侵袭能力显著降低(P < 0.001)。相反,过表达MYBL2增强了迁移和侵袭能力(P < 0.001)。在过表达或敲低MYBL2后,CDCA8与MYBL2基因和蛋白表达水平之间存在正相关(P < 0.001)。在致瘤性研究中,与对照组相比,敲低MYBL2组的肿瘤体积显著减小(P < 0.01),且肿瘤中CDCA8表达降低。
在本研究中,我们得出结论,MYBL2通过靶向调控CDCA8表达促进皮肤恶性黑色素瘤细胞的迁移、侵袭和增殖能力。