Nobiletin Inhibits Non-Small-Cell Lung Cancer by Inactivating WNT/ β-Catenin Signaling through Downregulating miR-15-5p

Sang Hyup Han; Jeong Hee Han; Wan Joo Chun; Sang Soo Lee; Hae Sung Kim; Jin Won Lee

doi:10.1155/2021/7782963

Nobiletin Inhibits Non-Small-Cell Lung Cancer by Inactivating WNT/ β-Catenin Signaling through Downregulating miR-15-5p

Evid Based Complement Alternat Med. 2021 Dec 30:2021:7782963. doi: 10.1155/2021/7782963. eCollection 2021.

Authors

Sang Hyup Han^{1

2}, Jeong Hee Han^{1

2}, Wan Joo Chun², Sang Soo Lee³, Hae Sung Kim^{1

2}, Jin Won Lee¹

Affiliations

¹ Department of Surgery, Chuncheon Sacred Heart Hospital, College of Medicine, Hallym University, Chuncheon 24253, Gangwon-Do, Republic of Korea.
² Department of Pharmacology, College of Medicine, The Kangwon University of Korea, Chuncheon, Republic of Korea.
³ Institute for Skeletal Aging & Orthopedic Surgery, Hallym University-Chuncheon Sacred Heart Hospital, Chuncheon, Republic of Korea.

Abstract

Background: Nobiletin is a natural compound with anticancer activity; however, the mechanism is not clear.

Methods: The inhibitory effect of nobiletin on non-small-cell lung cancer (NSCLC) cells was examined using soft agar, Transwell, and apoptosis analyses. Cancer stemness was measured by sphere assay. Genes and miRNAs regulated by nobiletin were identified by whole-genome sequencing. Protein levels were detected by western blot and immunofluorescence assays.

Results: Nobiletin significantly inhibited NSCLC cell colony formation and sphere formation and induced apoptosis. Nobiletin upregulated negative regulators of WNT/β-catenin signaling, including NKD1, AXIN2, and WIF1, while it inhibited the expression of β-catenin and its downstream genes, including c-Myc, c-Jun, and cyclin D1. Furthermore, we identified that GN inhibits miR-15-5p expression in NSCLC cells and that NKD1, AXIN2, and WIF1 are the target genes of miR-15-5p.

Conclusions: Nobiletin has a strong inhibitory effect on NSCLC, and nobiletin plays an anticancer role by inhibiting miR-15-5p/β-catenin signaling in NSCLC.