Detailed Information on Publication Record
2024
Role of the 3-mercaptopyruvate sulfurtransferase in colon/ colorectal cancers
MATYASOVA, Katarina, Andrea SOLTYSOVA, Petr BABULA, Oľga KRIŽANOVÁ, Veronika LISKOVA et. al.Basic information
Original name
Role of the 3-mercaptopyruvate sulfurtransferase in colon/ colorectal cancers
Authors
MATYASOVA, Katarina, Andrea SOLTYSOVA, Petr BABULA (203 Czech Republic, belonging to the institution), Oľga KRIŽANOVÁ (703 Slovakia, belonging to the institution) and Veronika LISKOVA
Edition
European Journal of Cell Biology, MUNICH, ELSEVIER GMBH, 2024, 0171-9335
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30105 Physiology
Country of publisher
Germany
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 6.600 in 2022
Organization unit
Faculty of Medicine
UT WoS
001230793100001
Keywords in English
mercaptopyruvate sulfurtransferase; Fission; Colon/colorectal cancer; Mitochondria
Tags
International impact, Reviewed
Změněno: 10/6/2024 10:11, Mgr. Tereza Miškechová
Abstract
V originále
The 3-mercaptopyruvate sulfurtransferase (MPST) is a protein persulfidase, occurring mainly in mitochondria. Although function of this protein in cancer cells has been already studied, no clear outcome can be postulated up to now. Therefore, we focused on the determination of function of MPST in colon (HCT116 cells)/colorectal (DLD1 cells) cancers. In silico analysis revealed that in gastrointestinal cancers, MPST together with its binding partners can be either of a high risk or might have a protective effect. Silencing of MPST gene resulted in decreased ATP, while acetyl-CoA levels were elevated. Increased apoptosis was detected in cells with silenced MPST gene, which was accompanied by decrease in mitochondrial membrane potential, but no changes in IP3 receptor's protein. Mitochondria underwent activation of fission and elevated DRP1 expression after MPST silencing. Proliferation and migration of DLD1 and HCT116 cells were markedly affected, showing the importance of MPST protein in colon/colorectal cancer development.