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Original Research

Open Access

Knockdown of NEIL3 inhibits the growth of breast cancer cells by mediating the PI3K/Akt/mTOR axis

  • Wanqiong Zheng1,*,
  • Ye Tian2
  • Yiming Zhang1
  • Binnan Li1

1Department of General surgery, Wenzhou Hospital of Integrated Traditional Chinese and Western Medicine, 325000 Wenzhou, Zhejiang, China

2Department of Oncology, Affiliated Hospital of Shaanxi University of Traditional Chinese Medicine, 712000 Xi’an, Shaanxi, China

DOI: 10.22514/ejgo.2025.042 Vol.46,Issue 3,March 2025 pp.105-111

Submitted: 11 November 2024 Accepted: 10 January 2025

Published: 15 March 2025

*Corresponding Author(s): Wanqiong Zheng E-mail: zwq5171717@163.com

Abstract

Background: To explore the role of Nei endonuclease VIII-like 3 (NEIL3) in breast cancer (BC) cell proliferation and motility and its underlying mechanism. Methods: BC cell lines were analyzed. NEIL3 expression levels in BC tissues was assessed using the UALCAN and Kaplan-Meier Plotter databases. NEIL3 knockdown was performed using siRNAs, and its effects on cell growth, motility, Epithelial-Mesenchymal Transition (EMT) markers, and the Phosphoinositide 3-Kinase/Protein Kinase B/Mammalian Target of Rapamycin (PI3K/Akt/mTOR) axis were evaluated using Immunoblotting, cell counting kit-8 (CCK-8) assays, colony formation, Transwell as well as wound healing assays. Results: NEIL3 was highly expressed in BC tissues and cell lines. NEIL3 knockdown inhibited cell growth, motility and reduced EMT marker expression. It also decreased phosphorylation levels of proteins, indicating inhibition of the PI3K/Akt/mTOR axis. Conclusions: NEIL3 mediates BC cell proliferation as well as motility by activating the PI3K/Akt/mTOR axis. Targeting NEIL3 may offer a new approach to combat BC.


Keywords

NEIL3; BC; PI3K/Akt/mTOR axis; Growth; Motility; EMT


Cite and Share

Wanqiong Zheng,Ye Tian,Yiming Zhang,Binnan Li. Knockdown of NEIL3 inhibits the growth of breast cancer cells by mediating the PI3K/Akt/mTOR axis. European Journal of Gynaecological Oncology. 2025. 46(3);105-111.

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