Evidence map›Paper›PMID 23471964›Full record

ArticleThe Journal of biological chemistry2013

Tumor-suppressive maspin functions as a reactive oxygen species scavenger: importance of cysteine residues.

Nitin Mahajan, Heidi Y Shi, Thomas J Lukas, Ming Zhang

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Role of RONS and eIFs in Cancer Progression.Oxidative medicine and cellular longevity · 2021
    Review
  7. Inhibition of miR-9 decreases osteosarcoma cell proliferation.Bosnian journal of basic medical sciences · 2020
    Article
  8. Maspin binds to cardiolipin in mitochondria and triggers apoptosis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  9. Sabotaging of the oxidative stress response by an oncogenic noncoding RNA.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  10. 1.45 Å resolution structure of SRPN18 from the malaria vector Anopheles gambiae.Acta crystallographica. Section F, Structural biology communications · 2016
    Article
  11. Signatures of prostate-derived Ets factor (PDEF) in cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
  12. 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

4 authors at 1 institution in 1 country.

Nitin MahajanDepartment of Molecular Pharmacology and Biological Chemistry and the Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA.
Heidi Y Shi
Thomas J Lukas
Ming Zhang
Robert H. Lurie Comprehensive Cancer Center of Northwestern University

Funding

THE ROLE OF MASPIN IN TUMOR METASTASIS &ANGIOGENESISR01CA079736 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZHANG, MING · 2000 to 2010
$3.2M
NCI NIH HHS CA79736NCI NIH HHS R01 CA079736
6 · The paper itself

Abstract

Maspin is a member of the serine protease inhibitor (serpin) superfamily and displays tumor-suppressing activity by controlling cell migration, proliferation, apoptosis, and adhesion. Here, we provide evidence that maspin acts as a reactive oxygen species (ROS) scavenger through oxidation of three structurally exposed cysteine thiols to sulfenic acid. Ablation of these cysteine residues in maspin resulted in a significant increase in total ROS production in mouse mammary TM40D cells. Also, cells containing a triple-cysteine mutant of maspin showed elevated ERK1/2 activity, a downstream target of ROS, and enhanced proliferation and colony formation. These findings establish a novel mechanism by which maspin utilizes its cysteine thiols to inhibit oxidative stress and cell growth.

Indexed as

Oxidative StressAmino Acid SubstitutionAnimalsCell Line, TumorCell ProliferationCysteineFemaleFree Radical ScavengersMAP Kinase Signaling SystemMiceMutation, MissenseOxidation-ReductionReactive Oxygen SpeciesSerpinsTumor Suppressor ProteinsCysteineFree Radical ScavengersReactive Oxygen SpeciesSERPIN-B5SerpinsTumor Suppressor Proteins

Identifiers

PMID23471964
PMCPMC3630891
OpenAlexW1974607999

What OpenQuestion holds

Textmetadata
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.