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Literature summary for 2.3.1.21 extracted from

  • Guan, L.; Chen, Y.; Wang, Y.; Zhang, H.; Fan, S.; Gao, Y.; Jiao, T.; Fu, K.; Sun, J.; Yu, A.; Huang, M.; Bi, H.
    Effects of carnitine palmitoyltransferases on cancer cellular senescence (2019), J. Cell. Physiol., 234, 1707-1719 .
    View publication on PubMed

Application

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

Localization Comment Organism GeneOntology No. Textmining
mitochondrion
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Homo sapiens 5739
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Organism

Organism UniProt Comment Textmining
Homo sapiens P23786 mitochondrial isoform isoform CTP1B
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Homo sapiens Q8TCG5 brain isoform CTP1C
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Homo sapiens Q92523 muscle isoform isoform CTP1B
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Source Tissue

Source Tissue Comment Organism Textmining
MDA-MB-231 cell
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Homo sapiens
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PANC-1 cell
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Homo sapiens
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General Information

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