Matches in SemOpenAlex for { <https://semopenalex.org/work/W2985896306> ?p ?o ?g. }
- W2985896306 endingPage "118573" @default.
- W2985896306 startingPage "118573" @default.
- W2985896306 abstract "Cytochrome c (Cyt c) released from mitochondria interacts with Apaf-1 to form the heptameric apoptosome, which initiates the caspase cascade to execute apoptosis. Although lysine residue at 72 (K72) of Cyt c plays an important role in the Cyt c-Apaf-1 interaction, the underlying mechanism of interaction between Cyt c and Apaf-1 is still not clearly defined. Here we identified multiple lysine residues including K72, which are also known to interact with ATP, to play a key role in Cyt c-Apaf-1 interaction. Mutation of these lysine residues abrogates the apoptosome formation causing inhibition of caspase activation. Using in-silico molecular docking, we have identified Cyt c-binding interface on Apaf-1. Although mutant Cyt c shows higher affinity for Apaf-1, the presence of Cyt c-WT restores the apoptosome activity. ATP addition modulates only mutant Cyt c binding to Apaf-1 but not WT Cyt c binding to Apaf-1. Using TCGA and cBioPortal, we identified multiple mutations in both Apaf-1 and Cyt c that are predicted to interfere with apoptosome assembly. We also demonstrate that transcript levels of various enzymes involved with dATP or ATP synthesis are increased in various cancers. Silencing of nucleotide metabolizing enzymes such as ribonucleotide reductase subunit M1 (RRM1) and ATP-producing glycolytic enzymes PKM2 attenuated ATP production and enhanced caspase activation. These findings suggest important role for lysine residues of Cyt c and nucleotides in the regulation of apoptosome-dependent apoptotic cell death as well as demonstrate how these mutations and nucleotides may have a pivotal role in human diseases such as cancer. • Lysine residues of Cyt c that interact with ATP are critical for apoptosome assembly. • Lysine mutations of Cyt c abrogate apoptosome formation and caspase activation. • Mutations of Apaf-1 and Cyt c in many cancers may hinder apoptosome function. • Silencing of RRM1/PKM2 attenuates ATP production and induces caspase activation. • Cyt c mutations and nucleotides may play a pivotal role in human disease prognosis." @default.
- W2985896306 created "2019-11-22" @default.
- W2985896306 creator A5001337472 @default.
- W2985896306 creator A5012219857 @default.
- W2985896306 creator A5012502014 @default.
- W2985896306 creator A5018809945 @default.
- W2985896306 creator A5020521540 @default.
- W2985896306 creator A5029186627 @default.
- W2985896306 creator A5034579434 @default.
- W2985896306 creator A5048603239 @default.
- W2985896306 creator A5054743749 @default.
- W2985896306 creator A5062006629 @default.
- W2985896306 creator A5063116970 @default.
- W2985896306 creator A5072916100 @default.
- W2985896306 date "2020-01-01" @default.
- W2985896306 modified "2023-10-07" @default.
- W2985896306 title "Molecular insights on cytochrome c and nucleotide regulation of apoptosome function and its implication in cancer" @default.
- W2985896306 cites W1440386396 @default.
- W2985896306 cites W1506642042 @default.
- W2985896306 cites W1968854074 @default.
- W2985896306 cites W1969855050 @default.
- W2985896306 cites W1973686119 @default.
- W2985896306 cites W1979039759 @default.
- W2985896306 cites W1984413324 @default.
- W2985896306 cites W1986889175 @default.
- W2985896306 cites W1995463051 @default.
- W2985896306 cites W1997099893 @default.
- W2985896306 cites W2004266769 @default.
- W2985896306 cites W2005089603 @default.
- W2985896306 cites W2008910497 @default.
- W2985896306 cites W2010364403 @default.
- W2985896306 cites W2011082535 @default.
- W2985896306 cites W2019042862 @default.
- W2985896306 cites W2024711136 @default.
- W2985896306 cites W2026228428 @default.
- W2985896306 cites W2029861821 @default.
- W2985896306 cites W2029877800 @default.
- W2985896306 cites W2037658687 @default.
- W2985896306 cites W2039375835 @default.
- W2985896306 cites W2040360153 @default.
- W2985896306 cites W2041058986 @default.
- W2985896306 cites W2044354161 @default.
- W2985896306 cites W2049717399 @default.
- W2985896306 cites W2050778896 @default.
- W2985896306 cites W2057428268 @default.
- W2985896306 cites W2058562137 @default.
- W2985896306 cites W2061427142 @default.
- W2985896306 cites W2079125529 @default.
- W2985896306 cites W2079705176 @default.
- W2985896306 cites W2087128996 @default.
- W2985896306 cites W2089496934 @default.
- W2985896306 cites W2094444045 @default.
- W2985896306 cites W2098817754 @default.
- W2985896306 cites W2100581111 @default.
- W2985896306 cites W2109171783 @default.
- W2985896306 cites W2114843025 @default.
- W2985896306 cites W2118477571 @default.
- W2985896306 cites W2119683782 @default.
- W2985896306 cites W2121818600 @default.
- W2985896306 cites W2122028337 @default.
- W2985896306 cites W2128469603 @default.
- W2985896306 cites W2128483394 @default.
- W2985896306 cites W2137315577 @default.
- W2985896306 cites W2140131019 @default.
- W2985896306 cites W2144701362 @default.
- W2985896306 cites W2146977885 @default.
- W2985896306 cites W2149441684 @default.
- W2985896306 cites W2151101199 @default.
- W2985896306 cites W2153983456 @default.
- W2985896306 cites W2154019529 @default.
- W2985896306 cites W2166239684 @default.
- W2985896306 cites W2170070595 @default.
- W2985896306 cites W2180388130 @default.
- W2985896306 cites W2273626774 @default.
- W2985896306 cites W2528337509 @default.
- W2985896306 cites W2556287713 @default.
- W2985896306 cites W2564122215 @default.
- W2985896306 cites W2577832018 @default.
- W2985896306 cites W2583882253 @default.
- W2985896306 cites W2768032770 @default.
- W2985896306 cites W2773240440 @default.
- W2985896306 cites W2789653144 @default.
- W2985896306 cites W2792253354 @default.
- W2985896306 cites W2890316895 @default.
- W2985896306 cites W2900706315 @default.
- W2985896306 cites W2902472954 @default.
- W2985896306 cites W2913106298 @default.
- W2985896306 cites W2920869071 @default.
- W2985896306 cites W4251279156 @default.
- W2985896306 doi "https://doi.org/10.1016/j.bbamcr.2019.118573" @default.
- W2985896306 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7733678" @default.
- W2985896306 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31678591" @default.
- W2985896306 hasPublicationYear "2020" @default.
- W2985896306 type Work @default.
- W2985896306 sameAs 2985896306 @default.
- W2985896306 citedByCount "20" @default.
- W2985896306 countsByYear W29858963062020 @default.
- W2985896306 countsByYear W29858963062021 @default.