z-logo
open-access-imgOpen Access
Demethoxycurcumin inhibits the growth of human lung cancer cells by targeting of PI3K/AKT/m-TOR signalling pathway, induction of apoptosis and inhibition of cell migration and invasion
Author(s) -
Yunlong Chen,
Mianhua Wu
Publication year - 2022
Publication title -
tropical journal of pharmaceutical research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.209
H-Index - 36
eISSN - 1596-5996
pISSN - 1596-9827
DOI - 10.4314/tjpr.v20i4.4
Subject(s) - pi3k/akt/mtor pathway , apoptosis , biology , protein kinase b , annexin , microbiology and biotechnology , cancer cell , viability assay , biochemistry , cancer , genetics
Purpose: To determine the antitumor effect of demethoxycurcumin on lung cancer cells, as well as its effect on PI3K/AKT/m-TOR signalling, cellular apoptosis, cell migration and cell invasion. Methods: Cell viability was determined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay, while AO/EB and annexin V/PI staining assays were used for apoptosis analysis in demethoxycurcumin-treated A-549 lung cancer cells. Transwell chamber assay was used to determine the effect of demethoxycurcumin on migration and invasion of A-549 cells. The expression levels of PI3K/AKT/m-TOR signalling and apoptosis-associated proteins in A-549 cells post- demethoxycurcumin treatment were determined by Western blotting assay. Results: Demethoxycurcumin markedly inhibited the proliferation of A-549 cells in a dose- and time- reliant fashion. The antiproliferative effect of demethoxycurcumin occurred via stimulation of apoptosis. The expression levels of Bax, Caspase-3 and Caspase-9 increased significantly, while Bcl-2 was significantly decreased in A-549 cells post-demethoxycurcumin treatment. Demethoxycurcumin substantially inhibited migration and invasion of A-549 cells, and blocked PI3K/AKT/m-TOR signalling pathway in these cells. Conclusion: Demethoxycurcumin induces anticancer effects on A-549 cells via targeting PI3K/AKT/mTOR signalling pathway. It induces cellular apoptosis and inhibits migration and invasion of A-549 cells. Thus, it is a promising anti-lung cancer agent.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom