Evidence map›Paper›PMID 18494001›Full record

ArticleJournal of cellular biochemistry2008

IFN-gamma regulation of vacuolar pH, cathepsin D processing and autophagy in mammary epithelial cells.

Zhila Khalkhali-Ellis, Daniel E Abbott, Caleb M Bailey, William Goossens, Naira V Margaryan, Stephen L Gluck, Moshe Reuveni, Mary J C Hendrix

Abstract read
In one paragraph

Article in Journal of cellular biochemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 26% 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 30 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. Type I interferon remodels lysosome function and modifies intestinal epithelial defense.Proceedings of the National Academy of Sciences of the United States of America · 2020
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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

8 authors at 2 institutions in 1 country.

Zhila Khalkhali-EllisChildren's Memorial Research Center, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60614-3394, USA. zellis@childrensmemorial.org
Daniel E Abbott
Caleb M Bailey
William Goossens
Naira V Margaryan
Stephen L Gluck
Moshe Reuveni
Mary J C Hendrix
Northwestern University · USUniversity of California, San Francisco · US

Funding

BIOLOGICAL FUNCTIONS OF MASPINR01CA075681 · NCI · UNIVERSITY OF IOWA · PI HENDRIX, MARY J.C. · 1997 to 2009
$1.7M
NCI NIH HHS CA 75681NCI NIH HHS R01 CA075681
6 · The paper itself

Abstract

In this study we examined the ability of interferon-gamma (IFN-gamma) to regulate mammary epithelial cell growth and gene expression, with particular emphasis on two genes: Maspin (a member of serine protease inhibitor superfamily), and the lysosomal aspartyl endopeptidase cathepsin D (CatD). The protein products of these genes are critically involved in regulation of multitude of biological functions in different stages of mammary tissue development and remodeling. In addition, the expression of Maspin is down-regulated in primary breast cancer and is lost in metastatic disease, while CatD is excessively produced and aberrantly secreted by breast cancer cells. We report that IFN-gamma receptors are expressed in mammary epithelial cells, and receptor engagement by IFN-gamma transduces the IFN-gamma signal via Stat-1 resulting in decreased vacuolar pH. This change in vacuolar pH alters CatD protein processing and secretion concurrent with increased Maspin secretion. In addition, IFN-gamma exerts a suppressive effect on cell growth and proliferation, and induces morphological changes in mammary epithelial cells. Our studies also reveal that breast cancer cells, which are devoid of Maspin, are refractory to IFN-gamma with respect to changes in vacuolar pH and CatD. However, Maspin transfection of breast cancer cells partially sensitizes the cells to IFN-gamma's effect, thus providing new therapeutic implications.

Indexed as

Apoptosis Regulatory ProteinsAutophagyBeclin-1Breast NeoplasmsCathepsin DCell LineEpithelial CellsGene Expression Regulation, EnzymologicHumansHydrogen-Ion ConcentrationInterferon-gammaMammary Glands, HumanMembrane ProteinsMicroscopy, Electron, TransmissionPhenotypeRNA, MessengerApoptosis Regulatory ProteinsBeclin-1BECN1 protein, humanCathepsin DInterferon-gammaMembrane ProteinsRNA, Messenger

Identifiers

PMID18494001
PMCPMC2575810
OpenAlexW2032969255

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.