Abstract

The abnormal expression in the T-type calcium channels is involved in various cancer types, thus inhibiting T-type calcium channels is one of approaches in cancer treatment. The fact that KTt-45 acted as a T-type calcium channel inhibitor as well as a pain-relief agent prompts us to address if KTt-45 plays any role against cancer cells. The results showed that KTt-45 caused cytotoxic effects towards HeLa cervical, Raji lymphoma, MCF-7 breast cancer, and A549 lung cancer cell lines with IC50 values less than 100 μM, in which highly selective toxicity was against HeLa cells (IC50 = 37.4 μM, SI > 3.2). Strikingly, the KTt-45 induced an accumulation of cytoplasmic vacuoles after 48 h treatment and mitochondrial-dependent apoptosis activation as evidenced by morphological features, chromatin condensation, nuclear fragmentation, and significant activation of caspase-9 as well as caspase-3. In conclusion, KTt-45 could inhibit cell growth and trigger mitochondrial-dependent apoptosis in HeLa cervical cancer cells. The results, taken together, strongly demonstrated that KTt-45 is a potential agent for further study on anticancer drug development which not only targets cancer cells but also helps to relieve neuropathic pain in cancer patients.

Details

Title
KTt-45, a T-type calcium channel blocker, acts as an anticancer agent by inducing apoptosis on HeLa cervical cancer cell line
Author
Du, Nguyen Huy 1 ; Ngoc, Truong Thi Bich 2 ; Cang, Huynh Qui 3 ; Luyen, Nguyen Thi Thuy 4 ; Thuoc, Tran Linh 3 ; Le Quan, Tran 4 ; Thao, Dang Thi Phuong 2 

 VNU-HCM, University of Science, Department of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, Ho Chi Minh City, Vietnam; VNU-HCM, University of Science, Laboratory of Cancer Research, Ho Chi Minh City, Vietnam (GRID:grid.493130.c) (ISNI:0000 0004 0567 1508); Vietnam National University, Ho Chi Minh City, Ho Chi Minh City, Vietnam (GRID:grid.267852.c) (ISNI:0000 0004 0637 2083); VNU-HCM, University of Science, Central Laboratory of Analysis, Ho Chi Minh City, Vietnam (GRID:grid.493130.c) (ISNI:0000 0004 0567 1508) 
 VNU-HCM, University of Science, Department of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, Ho Chi Minh City, Vietnam (GRID:grid.493130.c); VNU-HCM, University of Science, Laboratory of Cancer Research, Ho Chi Minh City, Vietnam (GRID:grid.493130.c) (ISNI:0000 0004 0567 1508); Vietnam National University, Ho Chi Minh City, Ho Chi Minh City, Vietnam (GRID:grid.267852.c) (ISNI:0000 0004 0637 2083) 
 VNU-HCM, University of Science, Laboratory of Cancer Research, Ho Chi Minh City, Vietnam (GRID:grid.493130.c) (ISNI:0000 0004 0567 1508); Vietnam National University, Ho Chi Minh City, Ho Chi Minh City, Vietnam (GRID:grid.267852.c) (ISNI:0000 0004 0637 2083) 
 Vietnam National University, Ho Chi Minh City, Ho Chi Minh City, Vietnam (GRID:grid.267852.c) (ISNI:0000 0004 0637 2083); VNU-HCM, University of Science, Central Laboratory of Analysis, Ho Chi Minh City, Vietnam (GRID:grid.493130.c) (ISNI:0000 0004 0567 1508); VNU-HCM, University of Science, Department of Hydro-Geology-Engineering Geology and Environmental Geology, Faculty of Geology, Ho Chi Minh City, Vietnam (GRID:grid.493130.c); VNU-HCM, University of Science, Department of Medicinal Chemistry, Faculty of Chemistry, Ho Chi Minh City, Vietnam (GRID:grid.493130.c) 
Pages
22092
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2900961686
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.