| Literature DB >> 34207708 |
Peiyu Wang1,2, Renwu Zhou3, Patrick Thomas1,2,4, Liqian Zhao5, Rusen Zhou3, Susmita Mandal6, Mohit Kumar Jolly6, Derek J Richard1,2, Bernd H A Rehm7, Kostya Ken Ostrikov8, Xiaofeng Dai9, Elizabeth D Williams1,2,3, Erik W Thompson1,2.
Abstract
Cold atmospheric plasma (CAP) has emerged as a highly selective anticancer agent, most recently in the form of plasma-activated medium (PAM). Since epithelial-mesenchymal transition (EMT) has been implicated in resistance to various cancer therapies, we assessed whether EMT status is associated with PAM response. Mesenchymal breast cancer cell lines, as well as the mesenchymal variant in an isogenic EMT/MET human breast cancer cell system (PMC42-ET/LA), were more sensitive to PAM treatment than their epithelial counterparts, contrary to their responses to other therapies. The same trend was seen in luminal muscle-invasive bladder cancer model (TSU-Pr1/B1/B2) and the non-muscle-invasive basal 5637 bladder cancer cell line. Three-dimensional spheroid cultures of the bladder cancer cell lines were less sensitive to the PAM treatment compared to their two-dimensional counterparts; however, incrementally better responses were again seen in more mesenchymally-shifted cell lines. This study provides evidence that PAM preferentially inhibits mesenchymally-shifted carcinoma cells, which have been associated with resistance to other therapies. Thus, PAM may represent a novel treatment that can selectively inhibit triple-negative breast cancers and a subset of aggressive bladder cancers, which tend to be more mesenchymal. Our approach may potentially be utilized for other aggressive cancers exhibiting EMT and opens new opportunities for CAP and PAM as a promising new onco-therapy.Entities:
Keywords: cold atmospheric plasma (CAP); epithelial–mesenchymal transition (EMT); plasma-activated medium (PAM); reactive oxygen species (ROS)
Year: 2021 PMID: 34207708 DOI: 10.3390/cancers13122889
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639