Zhao Zhirong, Zhan Yuanchang, Jing Li, Zhai Huali
Department of Clinical Laboratory, Xi'an Dian Medical Laboratory Co., Ltd., Xi'an Shaanxi 210016, P.R. China.
Department of Clinical Laboratory, Xi'an Aerospace General Hospital, Xi'an, Shaanxi 710000, P.R. China.
Oncol Lett. 2022 Jun;23(6):175. doi: 10.3892/ol.2022.13295. Epub 2022 Apr 13.
Malignant melanoma is a type of skin cancer caused by mutations in the DNA of melanocytes. Melanoma is relatively rare compared with other types of skin tumors, but has a highly aggressive biological behavior and consequently, a poorer prognosis. Therefore, the present study aimed to explore the role and mechanism of Kruppel-like factor 10 (KLF10) and acyl-CoA medium-chain synthetase 3 (ACSM3) in melanoma progression. KLF10 expression in melanoma tissues was predicted using Gene Expression Profiling Interactive Analysis (GEPIA). KLF10 expression in healthy and melanoma cells was also detected using reverse transcription-quantitative PCR and western blotting. Cell transfection was performed to overexpress KLF10 or silence ACSM3. Cell viability, proliferation, migration, invasion and apoptosis were detected using Cell Counting Kit-8, colony formation, wound healing, Transwell and TUNEL assays, respectively. The activity of the ACSM3 promoter was detected using a dual-luciferase reporter assay, and the relationship between KLF10 and ACSM3 was detected using the GEPIA database and chromatin immunoprecipitation (ChIP). The results demonstrated that KLF10 expression was significantly downregulated in melanoma cells, especially in A375 cells. Compared with the Ov-NC group, KLF10 overexpression significantly inhibited the proliferation, invasion and migration of melanoma cells and promoted their apoptosis. Similar to KLF10, ACSM3 was also downregulated in A375 cells compared with that in the HEM group, and the GEPIA database analysis and ChIP assay results demonstrated that KLF10 expression was positively associated with ACSM3 expression. Furthermore, silencing ACSM3 significantly reversed the effect of KLF10 overexpression on cell proliferation, invasion and migration, and ACSM3 knockdown increased the levels of phosphorylated (p)-PI3K and p-Akt compared with the levels in the Ov-KLF10 + sh-NC group. Overall, the present study suggested that KLF10 inhibited the proliferation, invasion and migration of melanoma cells by targeting ACSM3 via the PI3K/Akt signaling pathway.
恶性黑色素瘤是一种由黑素细胞DNA突变引起的皮肤癌。与其他类型的皮肤肿瘤相比,黑色素瘤相对少见,但具有高度侵袭性的生物学行为,因此预后较差。因此,本研究旨在探讨Kruppel样因子10(KLF10)和酰基辅酶A中链合成酶3(ACSM3)在黑色素瘤进展中的作用及机制。使用基因表达谱交互式分析(GEPIA)预测黑色素瘤组织中KLF10的表达。还使用逆转录定量PCR和蛋白质印迹法检测健康细胞和黑色素瘤细胞中KLF10的表达。进行细胞转染以过表达KLF10或沉默ACSM3。分别使用细胞计数试剂盒-8、集落形成、伤口愈合、Transwell和TUNEL检测法检测细胞活力、增殖、迁移、侵袭和凋亡。使用双荧光素酶报告基因检测法检测ACSM3启动子的活性,并使用GEPIA数据库和染色质免疫沉淀(ChIP)检测KLF10与ACSM3之间的关系。结果表明,黑色素瘤细胞中KLF10表达明显下调,尤其是在A375细胞中。与Ov-NC组相比,KLF10过表达显著抑制黑色素瘤细胞的增殖、侵袭和迁移,并促进其凋亡。与KLF10相似,与HEM组相比,A375细胞中ACSM3也下调,GEPIA数据库分析和ChIP检测结果表明KLF10表达与ACSM3表达呈正相关。此外,沉默ACSM3显著逆转了KLF10过表达对细胞增殖、侵袭和迁移的影响,与Ov-KLF10 + sh-NC组相比,ACSM3敲低增加了磷酸化(p)-PI3K和p-Akt的水平。总体而言,本研究表明KLF10通过PI3K/Akt信号通路靶向ACSM3抑制黑色素瘤细胞的增殖、侵袭和迁移。