1. Academic Validation
  2. Identification of an m6A Natural Inhibitor, Lobeline, That Reverses Lenvatinib Resistance in Hepatocellular Tumors

Identification of an m6A Natural Inhibitor, Lobeline, That Reverses Lenvatinib Resistance in Hepatocellular Tumors

  • J Nat Prod. 2024 Aug 23;87(8):1983-1993. doi: 10.1021/acs.jnatprod.4c00406.
Lei Zhao 1 Heyao Ma 2 Yuhui Jiang 3 Yingying Li 3 Li Qiao 3 Yu Chen 3 Xiaowen Jiang 4 Lihui Wang 3 Shu Wang 5 Xinyu Fan 6
Affiliations

Affiliations

  • 1 Department of Hepatobiliary and Pancreatic Surgery, The First Hospital of China Medical University, Shenyang, Liaoning 110001, China.
  • 2 Department of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning 110122, China.
  • 3 Department of Pharmacology, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • 4 Department of Analysis and Pharmacology of Traditional Chinese Medicine, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • 5 Department of Nuclear Medicine, The First Hospital of China Medical University, Shenyang, Liaoning 110001, China.
  • 6 Department of Pharmacy, Shengjing Hospital of China Medical University, Shenyang, Liaoning 110004, China.
Abstract

Hepatocellular carcinoma (HCC) is an aggressive Cancer that has an effect on human health. As a first-line drug for HCC, despite its excellent efficacy, lenvatinib (Len) is prone to developing drug resistance in HCC patients. The N6-methyladenosine (m6A) modification is not only related to the development of HCC but also shows great potential in overcoming HCC resistance. Using Dot Blot, our group first screened a small molecule m6A regulator, lobeline (Lob), from a library of 390 compounds (mostly Natural Products). In vitro experiments demonstrated that Lob could significantly enhance the sensitivity to Len of Len-resistant HCC (HCC/Len) and inhibit migration of resistant cells. In Len-resistant cell-derived and patient-derived xenograft models, Lob could reverse the resistant phenotype, with reductions in tumor volume of 68% and 60%, respectively. Furthermore, MeRIP-m6A Sequencing results indicated that the underlying molecular mechanism of Lob reversal of HCC drug resistance was related to UBE3B. Taken together, this study highlighted that Lob, a plant derived natural product, could reverse the resistance of HCC to Len by regulating the m6A levels. It is hoped that this will provide a pharmacological research basis for the clinical treatment of HCC patients.

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