Clerodane diterpene induces apoptosis/anoikis and suppresses migration and invasion of human bladder cancer cells through the histone deacetylases, integrin–focal adhesion kinase, and matrix metalloproteinase 9 signalling pathways. (23rd November 2022)

• Record Type: Journal Article
• Authors: Chen, Yu-Chi; Chen, Chih-I; Chang, Chao-Yuan; Huang, Bu-Miin; Chen, Yung-Chia
• Is Part Of: Human & experimental toxicology. Volume 41(2022)
• Publication Date: 2022-11-23
• Subjects: Bladder cancer -- 16-hydroxycleroda-3, 13-dien-15, 16-olide -- HDAC -- integrin signalling pathway; Toxicology -- Periodicals; 615.9
• DOI: 10.1177/09603271221143040
• Languages: English
• ISSNs: 0960-3271

Abstract

Clerodane diterpene, a class of bicyclic diterpenoids, is found in hundreds of plant species. 16-hydroxycleroda-3, 13-dien-15, 16-olide (CD) can be isolated from the plant Polyalthia longifol ia and has been applied against oral cancer and glioma by xenograft model. In this study, we aim to explore its antitumour action by examining its histone deacetylase (HDAC) activity and integrin-associated intracellular signalling pathway on T24 human bladder cancer (BC) cells. Our results revealed that CD-inhibited colony formation, HDAC activity, HDAC (1, 2 and 3) mRNA and cell spreading on fibronectin-coated surfaces in a concentration-dependent manner. Furthermore, decreased cFLIP and increased caspase-8 cleavage accompanied CD-induced cell death. At non-toxic concentrations, CD blocked the migration and invasion of T24 cells. CD hindered migration and invasion by the downregulation of fibronectin, integrin α 5 β 1, β -catenin, FAK, vinculin and Rho A, as well as by reduction of phosphorylated glycogen synthase kinase 3 β (pGSK3 β ), pSrc, pstat3 and pNF κ B. We observed that the MMP9 gene was closely linked with prognosis of patients with bladder cancer. MMP9 protein levels and activity were largely attenuated by CD in a concentration-dependent manner. In conclusion, CD-induced caspase-8-dependent apoptosis and suppressed migration and invasion by blocking several intracellular signalling pathways, including downregulation of HDAC activity and integrin–FAK and MMP9 pathways.