1. Academic Validation
  2. Therapeutic targeting m6A-guided miR-146a-5p signaling contributes to the melittin-induced selective suppression of bladder cancer

Therapeutic targeting m6A-guided miR-146a-5p signaling contributes to the melittin-induced selective suppression of bladder cancer

  • Cancer Lett. 2022 May 28;534:215615. doi: 10.1016/j.canlet.2022.215615.
Rucheng Yan 1 Weiwei Dai 2 Ruixin Wu 2 Houbao Huang 3 Minfeng Shu 4
Affiliations

Affiliations

  • 1 Department of Pharmacology, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, 131 Dong'an Road, Shanghai, 200032, PR China; Department of Urology, The First Affiliated Hospital (Yijishan Hospital) of Wannan Medical College, 2 Zheshan West Road, Wuhu, 241001, PR China.
  • 2 Department of Pharmacology, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, 131 Dong'an Road, Shanghai, 200032, PR China.
  • 3 Department of Urology, The First Affiliated Hospital (Yijishan Hospital) of Wannan Medical College, 2 Zheshan West Road, Wuhu, 241001, PR China. Electronic address: hhb@wnmc.edu.cn.
  • 4 Department of Pharmacology, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, 131 Dong'an Road, Shanghai, 200032, PR China; Ministry of Education (MOE) & Ministry of Health (MOH) Key Laboratory of Medical Molecular Virology, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, 131 Dong'an Road, Shanghai, 200032, PR China. Electronic address: minfeng_shu@fudan.edu.cn.
Abstract

Abnormal RNA methylation and dysregulation of miRNA are frequently occurred in bladder Cancer. Melittin is a potential drug candidate for intravesical chemotherapy against bladder Cancer. However, the underlying epigenetic mechanism by which melittin-induced anti-tumor effect remains unclear. Here, we showed that melittin selectively induced Apoptosis of bladder Cancer cells in a METTL3-dependent manner. Ectopic expression of METTL3 significantly blocked melittin-induced Apoptosis in vitro and in vivo. MicroRNA-sequence analysis identified miR-146a-5p suppression contributed to the melittin-induced selective antitumor effect. Further investigation revealed that METTL3-guided m6A modification methylated pri-miR-146 at the flanking sequence, which was responsible for the pri-miR-146 maturation. Moreover, NUMB/NOTCH2 axis was identified as a downstream target signal that mediated the pro-survival role of miR-146a-5p in bladder Cancer cells. Importantly, METTL3 and miR-146a-5p were positively correlated with recurrence and poor prognosis of patients with bladder Cancer. Our study indicates that METTL3 acts as a fate determinant that controls the sensitivity of bladder Cancer cells to melittin treatment. Moreover, METTL3/miR-146a-5p/NUMB/NOTCH2 axis plays an oncogenic role in bladder Cancer pathogenesis and could be a potential therapeutic target for recurrent bladder Cancer treatment.

Keywords

Apoptosis; METTL3; RNA methylation; Targeting therapy.

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