1. Academic Validation
  2. Poricoic Acid A, an Active Ingredient Extracted From Poria cocos, Inhibits Lung Cancer Cell Growth by Suppressing MEK/ERK Signaling Pathway

Poricoic Acid A, an Active Ingredient Extracted From Poria cocos, Inhibits Lung Cancer Cell Growth by Suppressing MEK/ERK Signaling Pathway

  • Phytother Res. 2025 Aug 27. doi: 10.1002/ptr.70080.
Xueni Sun 1 2 3 Haiyang Jiang 2 Shuyi Ren 2 Jing Xia 2 Jie Gu 2 Xiaoyu Sun 1 2 Yufei Huang 2 Zhiyu Zhu 2 Mengting Chen 2 Zehua Liao 2 Xinbing Sui 1 2 Yiping Mou 1
Affiliations

Affiliations

  • 1 Department of Gastrointestinal and Pancreatic Surgery, Key Laboratory of Gastroenterology of Zhejiang Province, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Zhejiang, Hangzhou, China.
  • 2 School of Pharmacy, Hangzhou Normal University, Zhejiang, Hangzhou, China.
  • 3 Department of Pathology and Pathophysiology, Zhejiang University School of Medicine, Hangzhou, China.
Abstract

Lung Cancer continues to be a significant clinical challenge, highlighting the urgent need for effective therapeutic strategies to improve patient outcomes. Poricoic acid A (PAA), an active compound derived from the traditional Chinese medicinal mushroom Poria cocos (Fuling), has gained attention for its potential antitumor effects. Although prior studies have suggested its efficacy in vitro, the therapeutic potential, mechanism of action, and safety of PAA in inhibiting Cancer growth have yet to be thoroughly investigated. The aim of this study was to explore the therapeutic potential of PAA against lung Cancer through comprehensive in vitro and in vivo experiments. In vitro, H460 and H1299 lung Cancer cells were treated with PAA to evaluate its impact on cell growth, Apoptosis, and the cell cycle using CCK-8 assay, colony formation assay, and flow cytometry analyses. In vivo, mouse models were used to assess both the efficacy of PAA in inhibiting tumor growth and its safety across primary organs. PAA significantly inhibited the growth of lung Cancer cells, induced Apoptosis, and caused cell cycle arrest in the G2/M phase. Mechanistic investigations revealed that PAA directly targeted MEK1/2, resulting in the downregulation of the MEK/ERK signaling pathway and subsequent suppression of cell growth and proliferation. In mouse models, PAA exhibited low toxicity and minimal adverse effects on primary organs. PAA holds promise as a potential therapeutic agent for lung Cancer, providing a solid foundation for future clinical investigation.

Keywords

MEK/ERK signaling pathway; anticancer activity; lung cancer; poricoic acid A.

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