Inhibition of Lonp1 induces mitochondrial remodeling and autophagy suppression in cervical cancer cells

• Published in: Acta histochemica Vol. 125; no. 1; p. 151986
• Main Authors: Wang, Xiaona, Xu, Xu, Zhao, Yu, Qi, Lifang, Ge, Hongshan
• Format: Journal Article
• Language: English
• Published: Germany Elsevier GmbH 01.01.2023
• Subjects: ATP-Dependent Proteases - genetics; ATP-Dependent Proteases - metabolism; Autophagy; Down-Regulation; Female; Humans; Lonp1; Mitochondria; Mitochondria - metabolism; Mitochondrial Proteins - genetics; Mitochondrial Proteins - metabolism; Uterine Cervical Neoplasms - genetics; Autophagy; Mitochondria; Lonp1
• ISSN: 0065-1281; 1618-0372
• DOI: 10.1016/j.acthis.2022.151986

Lon protease 1(Lonp1) is an ATP-dependent protease located in the mitochondrial matrix and plays a crucial role in preserving normal mitochondrial function. Lonp1 overexpression is associated with tumorigenesis in various cancer types, including cervical cancer. In the present study, we show that the Lonp1 content is elevated in cervical cancer tissues compared to cervical paracancerous tissues. Conversely, Lonp1 knockdown suppresses cervical cancer cell proliferation, migration and invasion but promotes apoptosis. Mechanistically, Lonp1 knockdown decreases area of mitochondrial networks and induces mitochondrial depolarization. Furthermore, Lonp1 inhibition reduces the level of LC3-II/I, PINK1 and Parkin, but promotes the level of p62. Collectively, our study suggests that the anti-cancer effect caused by Lonp1 downregulation likely contributes to mitochondrial remodeling and suppression of autophagy and mitophagy.