Arisaema heterophyllum Blume Monomer Stigmasterol Targets PPARγ and Inhibits the Viability and Tumorigenicity of Lung Adenocarcinoma Cells NCI-H1975

Author:

Song Na1,Wang Jing1,Lai Zonglang1,Liang Shuting2,Zou Wenjuan1,Wang Juan1,Zheng Dandan1,Li Ying3,He Yuxi4,Cheng Jun1ORCID,Wu Yue4ORCID

Affiliation:

1. Department of Oncolology, Chongqing Hospital of Traditional Chinese Medicine, Chongqing 400020, China

2. College of Chemical and Environmental Engineering, Chongqing University of Arts and Sciences, Chongqing 402160, China

3. Department of Nephrology, Chongqing Hospital of Traditional Chinese Medicine, Chongqing 400020, China

4. Department of Gastroenterology, Chongqing Hospital of Traditional Chinese Medicine, Chongqing 400020, China

Abstract

To clarify the regulatory effect and molecular mechanism of Arisaema heterophyllum Blume (AhBl) monomer stigmasterol on lung adenocarcinoma in human lung adenocarcinoma cells NCI-H1975 cultured in vitro and in nude mice. Oil red O staining, free fatty acid detection, adenosine triphosphate (ATP), and NADPH were applied to elucidate the regulatory effect of stigmasterol on the energy metabolism of NCI-H1975 cells. Simultaneously, colony formation assay and nude mouse tumorigenesis were performed to clarify the underlying mechanisms of stigmasterol on the proliferation and tumorigenesis of NCI-H1975 cells. Furthermore, peroxisome proliferator-activated receptor gamma (PPARγ) inhibitor GW9662 was supplemented to determine the expression changes of cyclins to clarify the regulation mechanism of stigmasterol. The results revealed that stigmasterol administration markedly inhibited the viability but promoted lipid deposition of NCI-H1975 cells. Meanwhile, the reduction of cell energy metabolism affected cell proliferation and colony formation. qPCR and western blot assays indicated that stigmasterol played a role in regulating the expression of cyclins and PPARγ signaling pathway proteins. Nude mouse tumorigenesis suggested that tumor size and weight in the stigmasterol-treated group were apparently lower as compared with the control group. Tumor tissue cells developed varying degrees of degeneration and large areas of ischemic necrosis presented in the central and peripheral cells. Immunohistochemistry results revealed that Ki67 expression in the stigmasterol group was substantially inhibited, while PPARγ expression was greatly elevated as compared with the control. GW9662 could mediate the inhibitory effect of stigmasterol on NCI-H1975 cells. The current study demonstrated that stigmasterol targeted PPARγ and inhibited the viability and tumorigenicity of lung adenocarcinoma cells NCI-H1975.

Funder

Chongqing Scientific Research Institution Performance Incentive and Guidance Special Project Description in 2020

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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