Evidence map›Paper›PMID 30661182›Full record

ArticleMolecular biology reports2019

Bag-1 silencing enhanced chemotherapeutic drug-induced apoptosis in MCF-7 breast cancer cells affecting PI3K/Akt/mTOR and MAPK signaling pathways.

Pelin Ozfiliz Kilbas, Izzet Mehmet Akcay, Gizem Dinler Doganay, Elif Damla Arisan

Abstract read
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In one paragraph

Article in Molecular biology reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. BAG family proteins contributes to autophagy-mediated multidrug resistance of tumor.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  5. Article
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  7. Review
  8. Article
  9. High-ThroughputFrontiers in oncology · 2021
    Article
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  12. Article
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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

4 authors at 2 institutions in 1 country.

Pelin Ozfiliz KilbasDepartment of Molecular Biology-Genetics and Biotechnology, Istanbul Technical University, Istanbul, Turkey.ORCID http://orcid.org/0000-0003-4386-934X
Izzet Mehmet AkcayDepartment of Molecular Biology-Genetics and Biotechnology, Istanbul Technical University, Istanbul, Turkey.ORCID http://orcid.org/0000-0001-6364-0062
Gizem Dinler DoganayDepartment of Molecular Biology-Genetics and Biotechnology, Istanbul Technical University, Istanbul, Turkey. gddoganay@itu.edu.tr.ORCID http://orcid.org/0000-0002-3586-1287
Elif Damla ArisanDepartment of Molecular Biology and Genetics, Istanbul Kultur University, Istanbul, Turkey. d.arisan@iku.edu.tr.ORCID http://orcid.org/0000-0002-4844-6381
Istanbul Kültür University · TRIstanbul Technical University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The multifunctional anti-apoptotic Bag-1 protein has important roles in apoptosis, proteasome-mediated degradation, transcriptional regulation, and intracellular signaling. Bag-1 promotes cell survival and proliferation, and is overexpressed in breast cancer. Therefore, Bag-1-targeted therapy might be a promising strategy to treat breast cancer. However, the effects of Bag-1 silencing in combination with conventional chemotherapeutic drugs on cell viability and major signaling pathways have not yet been fully investigated in breast cancer cells. In this study, we investigated the cytotoxic effects of Bag-1 silencing, alone and in combination with cisplatin or paclitaxel treatment, in MCF-7 breast cancer cells. Bag-1 knockdown by shRNA or siRNA transfection sensitized MCF-7 cells to apoptosis induced by cisplatin or paclitaxel. Combination of Bag-1 silencing and drug treatment more potently downregulated the pro-survival PI3K/Akt/mTOR and p44/42 mitogen activated protein kinase (MAPK) pathways, and more potently upregulated the stress-activated p38 and SAPK/JNK MAPK pathways. Bag-1-silenced drug-treated cells had also highly reduced proliferative capacity, downregulated cyclin-cyclin dependent kinase complexes and upregulated tumor suppressors p21 and Rb. These results overall indicated that Bag-1 silencing enhanced cisplatin- or paclitaxel-induced cytotoxicity through multiple pathways. In conclusion, Bag-1 targeted therapy might enhance the therapeutic potential of conventional anti-cancer drugs in the treatment of breast cancer.

Indexed as

ApoptosisGene SilencingAntineoplastic AgentsBreast NeoplasmsCaspasesCell CycleCell SurvivalCisplatinCyclin-Dependent KinasesDNA-Binding ProteinsDown-RegulationEnzyme ActivationFemaleHumansMAP Kinase Signaling SystemMCF-7 CellsAntineoplastic AgentsBCL2-associated athanogene 1 proteinCaspasesCisplatinCyclin-Dependent KinasesDNA-Binding ProteinsPaclitaxelPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesTranscription FactorsApoptosisBag-1 siRNA/shRNABreast cancerChemotherapeutic agentsMAPKPI3K/Akt/mTOR pathway

Identifiers

PMID30661182
OpenAlexW2909588163

What OpenQuestion holds

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Read underepoch 390

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.