Year: 2017
Type: article
Abstract: BACKGROUND/AIM: Anthracimycin, a secondary metabolite of Streptomyces, has been shown to inhibit the invasion of certain cancer cell lines. MATERIALS AND METHODS: In this study we evaluated the effect of anthracimycin on cell growth and signaling pathways in hepatocellular carcinoma (HCC). RESULTS: Anthracimycin suppressed cell proliferation and motility and induced apoptosis in human HCC cell lines. Furthermore, anthracimycin had no effect on the enrichment of EpCAM-high liver cancer stem cells (CSCs), while fluorouracil dramatically enriched the CSCs with activation of the stemness-related genes EPCAM and SOX9 in HuH7 cells. Mechanistically, anthracimycin suppressed mammalian target of rapamycin (mTOR) signaling, and was most effective at inhibiting HCC cell proliferation with mTOR activation. CONCLUSION: Anthracimycin is a novel mTOR inhibitor capable of suppressing the proliferation of CSCs and non-CSCs equally well in HCC, and it is suggested that anthracimycin could be effective in the eradication of HCC associated with mTOR-signaling activation.
Source: Anticancer Research
Authors: TOMOYUKI HAYASHI, TARO YAMASHITA, HIKARI OKADA, NAOKI OISHI, HAJIME SUNAGOZAKA, KOUKI NIO, TAKEHIRO HAYASHI, YASUMASA HARA, YOSHIRO ASAHINA, MARIKO YOSHIDA, TOMOMI HASHIBA, TSUYOSHI SUDA, TAKAYOSHI SHIRASAKI, YASUHIRO IGARASHI, KOJI MIYANOUCHI, TATSUYA YAMASHITA, MASAO HONDA, SHUICHI KANEKO
Institutions: Kanazawa University, Toyama Prefectural University
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
OpenAlex ID: W2965768804