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Plasma-activated medium inhibits cancer stem cell-like properties and exhibits a synergistic effect in combination with cisplatin in ovarian cancer

Authors
Lee, Young JooKim, Sung WookJung, Min HyungKim, Young SunKim, Kyung SookSuh, Dong SooKim, Ki HyungChoi, Eun HaKim, JongminKwon, Byung Su
Issue Date
Mar-2022
Publisher
Elsevier Inc.
Keywords
Cisplatin; Ovarian cancer stem cells; Plasma-activated medium; Synergistic cytotoxicity
Citation
Free Radical Biology and Medicine, v.182, pp 276 - 288
Pages
13
Journal Title
Free Radical Biology and Medicine
Volume
182
Start Page
276
End Page
288
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/151341
DOI
10.1016/j.freeradbiomed.2022.03.001
ISSN
0891-5849
1873-4596
Abstract
Ovarian cancer stem-like cells (CSCs) have been implicated in tumor recurrence, metastasis, and drug resistance. Accumulating evidence has demonstrated the antitumor effect of plasma-activated medium (PAM) in various carcinomas, including ovarian cancer. Thus, PAM represents a novel onco-therapeutic strategy. However, its impact on ovarian CSCs is unclear. Here, we show that ovarian CSCs resistant to high-dose conventional chemotherapeutic agents used for ovarian cancer treatment exhibited dose-dependent sensitivity to PAM. In addition, PAM treatment reduced the expression of stem cell markers and sphere formation, along with the aldehyde dehydrogenase- or CD133-positive cell population. We further investigated the effect of PAM in combination with other chemotherapeutics on ovarian CSCs in vitro. PAM exhibited synergistic cytotoxicity with cisplatin (CDDP) but not with paclitaxel and doxorubicin. In a peritoneal metastasis xenograft model established via intraperitoneal spheroid injection, PAM intraperitoneal therapy significantly suppressed peritoneal carcinomatosis (tumor size and number), with a more significant decrease observed due to the combined effects of PAM and CDDP with no side effects. Taken together, our results indicate that PAM inhibits ovarian CSC traits and exhibits synergetic cytotoxicity with CDDP, demonstrating PAM as a promising intraparietal chemotherapy for enhancing antitumor efficacy and reducing side effects. © The Authors
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