Evidence map›Paper›PMID 22729861›Full record

ReviewAdvances in experimental medicine and biology2012

Phosphorylation of mammalian cytochrome c and cytochrome c oxidase in the regulation of cell destiny: respiration, apoptosis, and human disease.

Maik Hüttemann, Icksoo Lee, Lawrence I Grossman, Jeffrey W Doan, Thomas H Sanderson

Open access · greenAbstract readReview
In one paragraph

Review in Advances in experimental medicine and biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
19.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 108 citations in OpenAlex.

  1. Pooled it
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  10. De novo sequencing and construction of a unique antibody for the recognition of alternative conformations of cytochromeProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Article
  12. Structural basis of mammalian complex IV inhibition by steroids.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Article
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  15. Review
  16. Review
  17. Article
  18. Post-Translational Modifications of CytochromeInternational journal of molecular sciences · 2020
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Maik HüttemannWayne State University School of Medicine, Detroit, MI, USA. mhuttema@med.wayne.edu
Icksoo Lee
Lawrence I Grossman
Jeffrey W Doan
Thomas H Sanderson
Wayne State University · USThe Barbara Ann Karmanos Cancer Institute · US

Funding

Regulation of Respiration and Apoptosis by Cytochrome c Phosphorylation.R01GM089900 · NIGMS · WAYNE STATE UNIVERSITY · PI HUETTEMANN, MAIK · 2010 to 2014
$1.4M
NIGMS NIH HHS GM089900NIGMS NIH HHS R01 GM089900
6 · The paper itself

Abstract

The mitochondrial oxidative phosphorylation (OxPhos) system not only generates the vast majority of cellular energy, but is also involved in the generation of reactive oxygen species (ROS), and apoptosis. Cytochrome c (Cytc) and cytochrome c oxidase (COX) represent the terminal step of the electron transport chain (ETC), the proposed rate-limiting reaction in mammals. Cytc and COX show unique regulatory features including allosteric regulation, isoform expression, and regulation through cell signaling pathways. This chapter focuses on the latter and discusses all mapped phosphorylation sites based on the crystal structures of COX and Cytc. Several signaling pathways have been identified that target COX including protein kinase A and C, receptor tyrosine kinase, and inflammatory signaling. In addition, four phosphorylation sites have been mapped on Cytc with potentially large implications due to its multiple functions including apoptosis, a pathway that is overactive in stressed cells but inactive in cancer. The role of COX and Cytc phosphorylation is reviewed in a human disease context, including cancer, inflammation, sepsis, asthma, and ischemia/reperfusion injury as seen in myocardial infarction and ischemic stroke.

Indexed as

ApoptosisCell RespirationAmino Acid SequenceAnimalsCyclic AMPCytochromes cElectron Transport Complex IVHumansInflammationMembrane Potential, MitochondrialMolecular Sequence DataNeoplasmsPhosphorylationProtein Kinase CReactive Oxygen SpeciesSignal TransductionCyclic AMPCytochromes cElectron Transport Complex IVProtein Kinase CReactive Oxygen Species

Identifiers

PMID22729861
PMCPMC3727645
OpenAlexW1507369121

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.