阿霉素
癌细胞
癌症
下调和上调
抑制器
异源的
癌症研究
化学
药物发现
细胞毒性
生物
基因
细胞生物学
生物化学
体外
化疗
遗传学
作者
Jaime Felipe Guerrero Garzón,Eva Madland,Martin Zehl,Madhurendra Singh,Shiva Rezaei,Finn L. Aachmann,Gastón Courtade,Ernst Urban,Christian Rückert,Tobias Busche,Jörn Kalinowski,Yan-Ru Cao,Yi Jiang,Cheng‐Lin Jiang,Galina Selivanova,Sergey B. Zotchev
出处
期刊:iScience
[Cell Press]
日期:2020-11-10
卷期号:23 (12): 101785-101785
被引量:17
标识
DOI:10.1016/j.isci.2020.101785
摘要
Heterologous expression of a biosynthesis gene cluster from Amycolatopsis sp. resulted in the discovery of two unique class IV lasso peptides, felipeptins A1 and A2. A mixture of felipeptins stimulated proliferation of cancer cells, while having no such effect on the normal cells. Detailed investigation revealed, that pre-treatment of cancer cells with a mixture of felipeptins resulted in downregulation of the tumor suppressor Rb, making the cancer cells to proliferate faster. Pre-treatment with felipeptins made cancer cells considerably more sensitive to the anticancer agent doxorubicin and re-sensitized doxorubicin-resistant cells to this drug. Structural characterization and binding experiments showed an interaction between felipeptins resulting in complex formation, which explains their synergistic effect. This discovery may open an alternative avenue in cancer treatment, helping to eliminate quiescent cells that often lead to cancer relapse.
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