Evidence map›Paper›PMID 26149967›Full record

ArticleScientific reports2015

Strategy to enhance efficacy of doxorubicin in solid tumor cells by methyl-β-cyclodextrin: Involvement of p53 and Fas receptor ligand complex.

Naoshad Mohammad, Shivendra Vikram Singh, Parmanand Malvi, Balkrishna Chaube, Dipti Athavale, Muralidharan Vanuopadath, Sudarslal Sadasivan Nair, Bipin Nair, Manoj Kumar Bhat

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

65 citing papers in PubMed, 117 citations in OpenAlex.

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  11. Journal of gastrointestinal oncology · 2022
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5 more citing papers are in PubMed but not listed here.

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

9 authors at 2 institutions in 1 country.

Naoshad MohammadNational Centre for Cell Science, Pune University Campus, Ganeshkhind, Pune- 411007, India.
Shivendra Vikram SinghNational Centre for Cell Science, Pune University Campus, Ganeshkhind, Pune- 411007, India.
Parmanand MalviNational Centre for Cell Science, Pune University Campus, Ganeshkhind, Pune- 411007, India.
Balkrishna ChaubeNational Centre for Cell Science, Pune University Campus, Ganeshkhind, Pune- 411007, India.
Dipti AthavaleNational Centre for Cell Science, Pune University Campus, Ganeshkhind, Pune- 411007, India.
Muralidharan VanuopadathAmrita School of Biotechnology, Amrita Vishwa Vidyapeetham University, Kollam-690525, India.
Sudarslal Sadasivan NairAmrita School of Biotechnology, Amrita Vishwa Vidyapeetham University, Kollam-690525, India.
Bipin NairAmrita School of Biotechnology, Amrita Vishwa Vidyapeetham University, Kollam-690525, India.
Manoj Kumar BhatNational Centre for Cell Science, Pune University Campus, Ganeshkhind, Pune- 411007, India.
National Centre for Cell Science · INAmrita Vishwa Vidyapeetham · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Doxorubicin (DOX) is one of the preferred drugs for treating breast and liver cancers. However, its clinical application is limited due to severe side effects and the accompanying drug resistance. In this context, we investigated the effect on therapeutic efficacy of DOX by cholesterol depleting agent methyl-β-cyclodextrin (MCD), and explored the involvement of p53. MCD sensitizes MCF-7 and Hepa1-6 cells to DOX, Combination of MCD and marginal dose of DOX reduces the cell viability, and promoted apoptosis through induction of pro-apoptotic protein, Bax, activation of caspase-8 and caspase-7, down regulation of anti-apoptotic protein Bcl-2 and finally promoting PARP cleavage. Mechanistically, sensitization to DOX by MCD was due to the induction of FasR/FasL pathway through p53 activation. Furthermore, inhibition of p53 by pharmacological inhibitor pifithrin-α (PFT-α) or its specific siRNA attenuated p53 function and down-regulated FasR/FasL, thereby preventing cell death. Animal experiments were performed using C57BL/6J mouse isografted with Hepa1-6 cells. Tumor growth was retarded and survival increased in mice administered MCD together with DOX to as compared to either agent alone. Collectively, these results suggest that MCD enhances the sensitivity to DOX for which wild type p53 is an important determinant.

Indexed as

AnimalsAntibiotics, AntineoplasticApoptosisbeta-CyclodextrinsCell Line, TumorCell SurvivalDoxorubicinDrug CarriersEnzyme-Linked Immunosorbent AssayFas Ligand Proteinfas ReceptorHumansImmunohistochemistryMaleMCF-7 CellsMiceAntibiotics, Antineoplasticbeta-CyclodextrinsDoxorubicinDrug CarriersFas Ligand Proteinfas Receptormethyl-beta-cyclodextrinRNA, Small InterferingTumor Suppressor Protein p53

Identifiers

PMID26149967
PMCPMC4493576
OpenAlexW2256666377

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LicenceCC BY
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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.