1‐Monopalmitin promotes lung cancer cells apoptosis through PI3K/Akt pathway in vitro

Author:

Niu Lulu1ORCID,Li Wenwen2,Chen Xin1,Su Xiaosan1,Dong Jingjing1,Liao Quanyang1,Zhou Xuhong1,Shi Shaoqing3,Sun Ruifen1

Affiliation:

1. Center for Scientific Research Yunnan University of Chinese Traditional Medicine Kunming Yunnan People's Republic of China

2. Department of Respiratory and Critical Care Medicine First Affiliated Hospital of Kunming Medical University Kunming People's Republic of China

3. Scientific Research Laboratory Center First Affiliated Hospital of Kunming Medical University Kunming Yunnan People's Republic of China

Abstract

AbstractLung cancer is the leading cause of cancer‐related death worldwide and non‐small cell lung cancer (NSCLC) represents 85%. Mougeotia nummuloides and Spirulina major have been reported to possess anticancer properties. 1‐Monopalmitin (1‐Mono) is the principle active constituent in these natural plants. It is debating whether 1‐Mono exerts antitumor effects. Therefore, we explored the role of 1‐Mono in lung cancer in vitro. Results showed that 1‐Mono significantly inhibited A549 and SPC‐A1 cell proliferation, induced G2/M arrest and caspase‐dependent apoptosis. Moreover, it suppressed the protein expression of inhibitors of apoptosis proteins (IAPs). It was further demonstrated that 1‐Mono activated the PI3K/Akt pathway, suppression of PI3K/Akt activities with LY294002 and Wortmannin partially attenuated 1‐Mono‐mediated anticancer activities, indicating that 1‐Mono‐induced antitumor effects is dependent on PI3K/Akt pathway. 1‐Mono induced cytoprotective autophagy since autophagy inhibitor Chloroquine dramatically enhanced 1‐Mono‐induced cytotoxicity. In summary, our results showed 1‐Mono kills lung cancer through PI3K/Akt pathway, providing novel options for lung cancer administration.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Management, Monitoring, Policy and Law,Toxicology,General Medicine

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