Hypermethylation of DLG3 Promoter Upregulates RAC1 and Activates the PI3K/AKT Signaling Pathway to Promote Breast Cancer Progression

Bingbing Liu; Yanning Xu; Lin Zhang; Xue Yang; Ling Chen; Yixin Liu

doi:10.1155/2021/8428130

Hypermethylation of DLG3 Promoter Upregulates RAC1 and Activates the PI3K/AKT Signaling Pathway to Promote Breast Cancer Progression

Evid Based Complement Alternat Med. 2021 Nov 2:2021:8428130. doi: 10.1155/2021/8428130. eCollection 2021.

Authors

Bingbing Liu¹, Yanning Xu¹, Lin Zhang¹, Xue Yang¹, Ling Chen¹, Yixin Liu¹

Affiliation

¹ Department of Pathology, Tianjin Central Hospital of Gynecology Obstetrics (Tianjin Key Laboratory of Human Development and Reproductive Regulation), Tianjin 300100, China.

Abstract

Objective: This investigation aimed to figure out the relation between discs large homolog 3 (DLG3) expression and the progression and prognosis of breast cancer (BC).

Methods: qRT-PCR was utilized for confirming DLG3 expression and RAC1 mRNA expression in BC tissues and cells. Subsequently, after overexpression or interference of DLG3, the changes of the biological activities of BC cells, including cell proliferation, migration, invasion, and apoptosis, were detected through CCK-8, colony formation assay, wound healing assay, transwell assay, and flow cytometry, respectively. Furthermore, western blotting was utilized to measure the protein expression of DLG3 and RAC1, as well as related proteins of epithelial-mesenchymal transition (EMT) and the PI3K/AKT signaling pathway.

Results: At both cellular and tissue level in BC, DLG3 was downregulated and methylation level was upregulated; RAC1 showed an opposite change and was of a negative correlation with DLG3. In MCF-7 and HCC1937, we found that the upregulation of DLG3 could inhibit RAC1 expression as well as cell proliferation, invasion, migration, and EMT, while promoting apoptosis. Also, DLG3 inhibited the activation of the P13K/AKT pathway.

Conclusion: Hypermethylation of DLG3 promoter upregulates RAC1 and activates the PI3K/AKT pathway, thus promoting BC progression. This conclusion provides ideas and experimental basis for improving and treating BC patients.