Berberrubine is a novel and selective IMPDH2 inhibitor that impairs the growth of colorectal cancer

[Display omitted] Inosine monophosphate dehydrogenase (IMPDH) catalyzes the rate-limiting reaction in the de novo synthesis pathway of guanine nucleotides that is highly required for cancer cell outgrowth. Herein, we found that IMPDH isoform 2 (IMPDH2) is highly expressed in colorectal cancer (CRC)...

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Veröffentlicht in:Biochemical pharmacology 2023-12, Vol.218, p.115868-115868, Article 115868
Hauptverfasser: He, Xiangli, Cui, Jiayan, Ma, Hui, Abuduaini, Naijipu, Huang, Ying, Tang, Lu, Wang, Wanyan, Zhang, Yuanyuan, Wang, Yang, Lu, Weiqiang, Feng, Bo, Huang, Jin
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Sprache:eng
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Zusammenfassung:[Display omitted] Inosine monophosphate dehydrogenase (IMPDH) catalyzes the rate-limiting reaction in the de novo synthesis pathway of guanine nucleotides that is highly required for cancer cell outgrowth. Herein, we found that IMPDH isoform 2 (IMPDH2) is highly expressed in colorectal cancer (CRC) and is correlated with poor patient prognosis. Via structure-based virtual screening, we identified berberrubine, a critical ingredient of the medical plant Coptis chinensis, as a novel, selective, and competitive inhibitor of IMPDH2, which demonstrated over 15-fold selectivity to IMPDH2 than IMPDH1. Besides, we also confirmed the interaction between berberrubine and IMPDH2. Of note, berberrubine treatment significantly impairs the growth of human CRC cells in a dose-dependent manner, which can be rescued by supplementing with guanosine. Furthermore, oral administration of berberrubine remarkably reduced tumor volume and weight in a human cell line-derived xenograft model. Importantly, the anti-cancer activity of berberrubine was also confirmed by using the azoxymethane (AOM) / dextran sulfate sodium (DSS)-induced spontaneous CRC mouse model. Taken together, our study highlights that berberrubine acts as a novel IMPDH2 inhibitor, suppressing the growth of CRC in vitro and in vivo, providing a fresh perspective for its potential application in the treatment of CRC.
ISSN:0006-2952
1873-2968
DOI:10.1016/j.bcp.2023.115868