1. Academic Validation
  2. GPER agonist G-1 activates YAP to induce apoptosis in breast cancer cells

GPER agonist G-1 activates YAP to induce apoptosis in breast cancer cells

  • J Steroid Biochem Mol Biol. 2025 Apr:248:106693. doi: 10.1016/j.jsbmb.2025.106693.
Ze Fu 1 Xin Xin 1 Yongtong Zhan 1 Xuhong Fan 1 Xin Li 1 Tongsheng Chen 2 Xiaoping Wang 3
Affiliations

Affiliations

  • 1 Department of Pain Management, The First Affiliated Hospital of Jinan University, Guangzhou 510630, China.
  • 2 MOE Key Laboratory of Laser Life Science & Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China.
  • 3 Department of Pain Management, The First Affiliated Hospital of Jinan University, Guangzhou 510630, China. Electronic address: txp2938@jnu.edu.cn.
Abstract

G-1, a G protein-coupled Estrogen Receptor (GPER)-specific agonist, exhibits Anticancer potential in breast Cancer cells. This study aims to explore the molecular basis of Apoptosis induced by G-1 in MCF-7 and MDA-MB-231 breast Cancer cells. Here, we found that G-1 induced cytotoxicity and GPER-dependent Apoptosis with PARP cleavage and mitochondrial membrane potential (MMP) loss, as well as nuclear condensation. Fluorescence resonance energy transfer (FRET) analysis in living cells indicated that G-1 effectively disrupted the interaction between large tumor suppressor 1/2 (LATS1/2) and Yes-associated protein (YAP). Furthermore, G-1 reduced YAP phosphorylation levels and promoted its nuclear accumulation. Notably, knockdown of YAP attenuated G-1-induced Apoptosis, highlighting the crucial role of YAP in this process. Additionally, FRET analysis revealed that G-1 enhanced the binding of YAP to p73, leading to an increase in Bcl-2-associated X protein (Bax) expression and an induction of Apoptosis. In summary, our findings demonstrate that G-1 induces Apoptosis through the GPER/YAP/p73-mediated pathway.

Keywords

Apoptosis; Breast cancer; G-1; GPER; YAP.

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