Hederacolchiside A1 Suppresses Autophagy by Inhibiting Cathepsin C and Reduces the Growth of Colon Cancer

While autophagy degrades non-functional or unnecessary cellular components, producing materials for synthesizing cellular components, it can also provide energy for tumor development. Hederacolchiside A1 (HA1) derived from has anticancer effects on several carcinomas by inducing apoptosis or exhibit...

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Veröffentlicht in:Cancers 2023-02, Vol.15 (4), p.1272
Hauptverfasser: Kim, Solbi, Lee, Kyung-Ha, Choi, Hui-Ji, Kim, Eunji, Kang, Sora, Han, Minju, Jeon, Heung Jin, Yun, Mi-Young, Song, Gyu-Yong, Lee, Hyo Jin
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Sprache:eng
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Zusammenfassung:While autophagy degrades non-functional or unnecessary cellular components, producing materials for synthesizing cellular components, it can also provide energy for tumor development. Hederacolchiside A1 (HA1) derived from has anticancer effects on several carcinomas by inducing apoptosis or exhibiting cytotoxicity, but the relationship with autophagy has not been studied. We investigated the association between HA1 and autophagy and evaluated its anticancer effect on colon cancer. HA1 induced accumulation of the autophagy-related markers LC3B and SQSTM1, with distinct vacuolar formation, unlike other autophagy inhibitors; the effects were similar to those of chloroquine. In addition, HA1 decreased the expression and proteolytic activity of lysosomal protein cathepsin C, reduced the growth of colon cancer cells , and inhibited tumor growth . It also reduced the expression of Ki-67 and cathepsin C in mouse tissues and reduced the growth of spheroids and organoids composed of cancer cells. Taken together, these results imply that HA1 regulates cell growth and autophagy and has potential as a promising therapeutic agent in colon cancer.
ISSN:2072-6694
2072-6694
DOI:10.3390/cancers15041272