MLLT11 siRNA抑制MDA-MB-231乳腺癌细胞迁移并促进细胞凋亡

Xiangrong Liu, Wenqi Bai, Jianrong Li, Jinfeng Ma, Yan Liu, Zhixiang Wang, Linjie Hu, Zheng Li, Dimitri Papukashvili, Nino Rcheulishvili, Fusheng Wang, Xiaoqing Lu
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引用次数: 0

摘要

乳腺癌被认为是最普遍的恶性肿瘤,因为它在女性中发病率高,复发和转移,使其成为最致命的癌症之一。目前的研究旨在预测与乳腺癌复发和转移相关的基因,并验证它们对MDA-MB-231细胞的影响。通过生物信息学分析,获得转录因子7辅因子(MLLT11)作为靶基因。合成mllt11特异性siRNA并转染到MDA-MB-231细胞中。结果表明,siRNA显著降低了MLLT11 mRNA水平。此外,siRNA处理组细胞迁移和侵袭,以及磷脂酰肌醇3-激酶(PI3K)、AKT、基质金属蛋白酶(MMP) 2和MMP9蛋白水平显著降低,细胞凋亡增加。总的来说,MLLT11 siRNA可能通过抑制PI3K/AKT信号通路,引发乳腺癌细胞的改善特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MLLT11 siRNA Inhibits the Migration and Promotes the Apoptosis of MDA-MB-231 Breast Cancer Cells
Breast cancer is considered the most prevalent malignancy due to its high incidence rate, recurrence, and metastasis in women that makes it one of the deadliest cancers. The current study aimed to predict the genes associated with the recurrence and metastasis of breast cancer and to validate their effect on MDA-MB-231 cells. Through the bioinformatics analysis, the transcription factor 7 cofactor (MLLT11) as the target gene was obtained. MLLT11-specific siRNA was synthesized and transfected into MDA-MB-231 cells. The results demonstrated that the siRNA significantly reduced the MLLT11 mRNA levels. Moreover, cell migration and invasion, as well as the protein levels of phosphatidylinositol 3-kinase (PI3K), AKT, matrix metalloproteinase (MMP) 2, and MMP9, were significantly lower in the groups treated with siRNA while the apoptosis was augmented. Collectively, MLLT11 siRNA elicited ameliorative properties on breast cancer cells, possibly via the inhibition of the PI3K/AKT signaling pathway.
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