Application | Comment | Organism |
---|---|---|
medicine | compared to isoforms CPT1A, CPT1B and CPT2, isoform CPT1C exerts the most significant effect on mitochondrial dysfunction-associated tumor cellular senescence among the members of the CPT family | Homo sapiens |
Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|
mitochondrion | - |
Homo sapiens | 5739 | - |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | P23786 | mitochondrial isoform isoform CTP1B | - |
Homo sapiens | Q8TCG5 | brain isoform CTP1C | - |
Homo sapiens | Q92523 | muscle isoform isoform CTP1B | - |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
MDA-MB-231 cell | - |
Homo sapiens | - |
PANC-1 cell | - |
Homo sapiens | - |
General Information | Comment | Organism |
---|---|---|
physiological function | silencing of CPT1C by siRNA leads to a significant decrease in DNA synthesis and weaker colony-forming capacities in PANC-1 and MDA-MB-231 cells. CPT1C-depleted PANC-1 and MDA-MB-231 cells arrest the cell cycle in G1 phase, changing this cell population from 30.0% to 58.0% and 50.3% to 56.0%, respectively. Silencing increases intracellular lipid content by 1.45fold. CPT1C knockdown cells accumulate intracellular ROS, compared with the negative control, by 2.8fold and causes rapid RH123 dequenching to 36.8%, which impairs the mitochondrial electrochemical gradient and permeability transition | Homo sapiens |
physiological function | silencing of CPT2 by siRNA leads to a decrease in DNA synthesis, decreases replicating DNA by 19.9% in MDA-MB-231 cells, and results in weaker colony-forming capacities. CPT1B-depleted PANC-1 and MDA-MB-231 cells arrest the cell cycle in G1 phase. Knockdown of CPT2 downregulates the mRNA levels of ERRbeta/gamma, GABPalpha, CREB and upregulates CISD1 | Homo sapiens |