Evidence map›Paper›PMID 33515365›Full record

ArticleThe protein journal2021

Jasplakinolide Attenuates Cell Migration by Impeding Alpha-1-syntrophin Protein Phosphorylation in Breast Cancer Cells.

Roshia Ali, Hilal Ahmad Mir, Rabia Hamid, Riaz A Shah, Firdous A Khanday, Sahar Saleem Bhat

Abstract read
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Article in The protein journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

13 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Roles of the cytoskeleton in human diseases.Molecular biology reports · 2023
    Review
  10. Article
  11. Article
  12. Actin stabilization in cell migration.Frontiers in cell and developmental biology · 2022
    Article
  13. 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

6 authors at 2 institutions in 1 country.

Roshia AliDepartment of Biotechnology, University of Kashmir, Hazratbal, Srinagar, J&K, 190006, India.
Hilal Ahmad MirDepartment of Biotechnology, University of Kashmir, Hazratbal, Srinagar, J&K, 190006, India.
Rabia HamidDepartment of Nanotechnology, University of Kashmir, Srinagar, J&K, 190006, India.
Riaz A ShahDivision of Biotechnology, FVSc & AH, SKUAST-K, Shuhama, Srinagar, J&K, India.
Firdous A KhandayDepartment of Biotechnology, University of Kashmir, Hazratbal, Srinagar, J&K, 190006, India. khandayf@kashmiruniversity.ac.in.
Sahar Saleem BhatDivision of Biotechnology, FVSc & AH, SKUAST-K, Shuhama, Srinagar, J&K, India. saleem.sehar@gmail.com.ORCID 0000-0002-0492-2753
University of Kashmir · INSher-e-Kashmir University of Agricultural Sciences and Technology of Kashmir · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlpha-1-syntrophin (SNTA1) is emerging as a novel modulator of the actin cytoskeleton. SNTA1 binds to F-actin and regulates intracellular localization and activity of various actin organizing signaling molecules. Aberration in syntrophin signaling has been closely linked with deregulated growth connected to tumor development/metastasis and its abnormal over expression has been observed in breast cancer. In the present work the effect of jasplakinolide, an actin-binding cyclodepsipeptide, on the SNTA1 protein activity and SNTA1 mediated downstream cellular events was studied in MDA-MB-231 breast cancer cell line.

methodsSNTA1 protein levels and phosphorylation status were determined in MDA-MB-231 cells post jasplakinolide exposure using western blotting and immunoprecipitation techniques respectively. MDA-MB-231 cells were transfected with WT SNTA1 and DM SNTA1 (Y

resultsJasplakinolide treatment decreases proliferation of MDA-MB-231 cells in both dose and time dependent manner. Results suggest that subtoxic doses of jasplakinolide induce morphological changes in MDA-MB-231 cells from flat spindle shape adherent cells to round weakly adherent forms. Mechanistically, jasplakinolide treatment was found to decrease SNTA1 protein levels and its tyrosine phosphorylation status. Moreover, migratory potential of jasplakinolide treated cells was significantly inhibited in comparison to control cells.

conclusionOur results demonstrate that jasplakinolide inhibits cell migration by impairing SNTA1 functioning in breast cancer cells.

Indexed as

Calcium-Binding ProteinsDepsipeptidesMembrane ProteinsMuscle ProteinsBreast NeoplasmsCell Line, TumorCell MovementCell SurvivalFemaleHumansPhosphorylationCalcium-Binding ProteinsDepsipeptidesjasplakinolideMembrane ProteinsMuscle Proteinssyntrophin alpha1Actin polymerizationAlpha-1-syntrophinBreast cancerJasplakinolideMigration

Identifiers

PMID33515365
OpenAlexW3124716527

What OpenQuestion holds

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Registered trials

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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.