MLLT11 siRNA Inhibits the Migration and Promotes the Apoptosis of MDA-MB-231 Breast Cancer Cells

Author:

Liu Xiangrong1,Bai Wenqi2ORCID,Li Jianrong1,Ma Jinfeng1ORCID,Liu Yan3,Wang Zhixiang3,Hu Linjie3,Li Zheng3,Papukashvili Dimitri4ORCID,Rcheulishvili Nino4ORCID,Wang Fusheng2ORCID,Lu Xiaoqing1ORCID

Affiliation:

1. Shanxi Province Cancer Hospital, Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences, Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan 030001, China

2. Breast Surgery, The Second Hospital of Shanxi Medical University, Taiyuan 030001, China

3. Shanxi Medical University, Taiyuan 030006, China

4. Southern University of Science and Technology, Shenzhen 518055, China

Abstract

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.

Funder

National Natural Science Foundation of China

Publisher

Hindawi Limited

Subject

Oncology,Surgery,Internal Medicine

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