Evidence map›Paper›PMID 15713631›Full record

ArticleMolecular and cellular biology2005

Maspin mediates increased tumor cell apoptosis upon induction of the mitochondrial permeability transition.

Khatri Latha, Weiguo Zhang, Nathalie Cella, Heidi Y Shi, Ming Zhang

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Iripin-3, a New Salivary Protein Isolated FromFrontiers in immunology · 2021
    Article
  11. Zinc oxide nanoparticles enhance expression of maspin in human breast cancer cells.Environmental science and pollution research international · 2020
    Article
  12. Article
  13. Article
  14. Maspin binds to cardiolipin in mitochondria and triggers apoptosis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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 1 institution in 1 country.

Khatri LathaDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA.
Weiguo Zhang
Nathalie Cella
Heidi Y Shi
Ming Zhang
Baylor College of Medicine · US

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 unique serpin with the ability to suppress certain types of malignant tumors. It is one of the few p53-targeted genes involved in tumor invasion and metastasis. With this in mind, we attempted to study the molecular mechanism behind this tumor suppression. Maspin-expressing mammary tumors are more susceptible to apoptosis in both implanted mammary tumors in vivo, a three-dimensional spheroid culture system, as well as in monolayer cell culture under lowered growth factors. Subcellular fractionation shows that a fraction of maspin (in both TM40D-Mp and mutant maspinDeltaN cells) translocates to the mitochondria. This translocation of maspin to the mitochondria is linked to the opening of the permeability transition pore, which in turn causes the loss of transmembrane potential, thus initiating apoptotic degradation. This translocation is absent in the other mutant, maspinDeltaRSL. It fails to cause any loss of membrane potential and also shows decreased caspase 3 levels, proving that translocation to the mitochondria is a key event for this increase in apoptosis by maspin. Suppression of maspin overexpression by RNA interference desensitizes cells to apoptosis. Our data indicate that maspin inhibits tumor progression through the mitochondrial apoptosis pathway. These findings will be useful for maspin-based therapeutic interventions against breast cancer.

Indexed as

ApoptosisAnimalsCaspase 3CaspasesCytochromes cGenes, Tumor SuppressorHumansImmunoprecipitationIon ChannelsMammary Neoplasms, ExperimentalMembrane PotentialsMiceMitochondriaMitochondrial Membrane Transport ProteinsMitochondrial Permeability Transition PoreProteinsCASP3 protein, humanCasp3 protein, mouseCaspase 3CaspasesCytochromes cIon ChannelsMitochondrial Membrane Transport ProteinsMitochondrial Permeability Transition PoreProteinsSERPIN-B5SerpinsTumor Suppressor Proteins

Identifiers

PMID15713631
PMCPMC549349
OpenAlexW2155225564

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.