Journal of Pharmaceutical Analysis (Mar 2025)

Elemene as a binding stabilizer of microRNA-145-5p suppresses the growth of non-small cell lung cancer

  • Meirong Zhou,
  • Jiayue Wang,
  • Yulin Peng,
  • Xiangge Tian,
  • Wen Zhang,
  • Junlin Chen,
  • Yue Wang,
  • Yu Wang,
  • Youjian Yang,
  • Yongwei Zhang,
  • Xiaokui Huo,
  • Yuzhuo Wu,
  • Zhenlong Yu,
  • Tian Xie,
  • Xiaochi Ma

Journal volume & issue
Vol. 15, no. 3
p. 101118

Abstract

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Elemene is widely recognized as an effective anti-cancer compound and is routinely administered in Chinese clinical settings for the management of several solid tumors, including non-small cell lung cancer (NSCLC). However, its detailed molecular mechanism has not been adequately demonstrated. In this research, it was demonstrated that elemene effectively curtailed NSCLC growth in the patient-derived xenograft (PDX) model. Mechanistically, employing high-throughput screening techniques and subsequent biochemical validations such as microscale thermophoresis (MST), microRNA-145-5p (miR-145-5p) was pinpointed as a critical target through which elemene exerts its anti-tumor effects. Interestingly, elemene serves as a binding stabilizer for miR-145-5p, demonstrating a strong binding affinity (dissociation constant (KD) = 0.39 ± 0.17 μg/mL) and preventing its degradation both in vitro and in vivo, while not interfering with the synthesis of the primary microRNA transcripts (pri-miRNAs) and precursor miRNAs (pre-miRNAs). The stabilization of miR-145-5p by elemene resulted in an increased level of this miRNA, subsequently suppressing NSCLC progression through the miR-145-5p/mitogen-activated protein kinase kinase kinase 3 (MAP3K3)/nuclear factor kappaB (NF-κB) pathway. Our findings provide a new perspective on revealing the interaction patterns between clinical anti-tumor drugs and miRNAs.

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