Evidence map›Paper›PMID 27922047›Full record

ArticleScientific reports2016

New arylated benzo[h]quinolines induce anti-cancer activity by oxidative stress-mediated DNA damage.

Dharmendra K Yadav, Reeta Rai, Naresh Kumar, Surjeet Singh, Sanjeev Misra, Praveen Sharma, Priyanka Shaw, Horacio Pérez-Sánchez, Ricardo L Mancera, Eun Ha Choi and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 63 citations in OpenAlex.

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  16. Molecular interaction of tea catechin with bovine β-lactoglobulin: A spectroscopic and in silico studies.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2020
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  20. Surfen-mediated blockade of extratumoral chondroitin sulfate glycosaminoglycans inhibits glioblastoma invasion.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
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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

12 authors at 7 institutions in 4 countries.

Dharmendra K YadavDepartment of Biochemistry, All India Institute of Medical Sciences, Jodhpur-342005, India.
Reeta RaiDepartment of Biochemistry, All India Institute of Medical Sciences, New Delhi-110029, India.
Naresh KumarPlasma Bioscience Research Center, Kwangwoon University, Nowon-Gu, Seoul 139-701, Korea.
Surjeet SinghDepartment of Chemistry, University of Delhi-110007 India.
Sanjeev MisraDepartment of Biochemistry, All India Institute of Medical Sciences, Jodhpur-342005, India.
Praveen SharmaDepartment of Biochemistry, All India Institute of Medical Sciences, Jodhpur-342005, India.
Priyanka ShawPlasma Bioscience Research Center, Kwangwoon University, Nowon-Gu, Seoul 139-701, Korea.
Horacio Pérez-SánchezComputer Science Department, Catholic University of Murcia (UCAM) E30107, Murcia, Spain.
Ricardo L ManceraSchool of Biomedical Sciences, Curtin Health Innovation Research Institute and Curtin Institute for Computation, Curtin University: GPO Box U1987, Perth WA 6845, Australia.
Eun Ha ChoiPlasma Bioscience Research Center, Kwangwoon University, Nowon-Gu, Seoul 139-701, Korea.
Mi-Hyun KimDepartment of Pharmacy, College of Pharmacy, Gachon University, 155 Gaetbeol-ro, Incheon, Korea.
Ramendra PratapDepartment of Chemistry, University of Delhi-110007 India.
All India Institute of Medical Sciences Jodhpur · INKwangwoon University · KRUniversity of Delhi · INAll India Institute of Medical Sciences · INCurtin University · AUGachon University · KRUniversidad Católica San Antonio de Murcia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The anti-cancer activity of the benzo[h]quinolines was evaluated on cultured human skin cancer (G361), lung cancer (H460), breast cancer (MCF7) and colon cancer (HCT116) cell lines. The inhibitory effect of these compounds on the cell growth was determined by the MTT assay. The compounds 3e, 3f, 3h and 3j showed potential cytotoxicity against these human cancer cell lines. Effect of active compounds on DNA oxidation and expression of apoptosis related gene was studied. We also developed a quantitative method to measure the activity of cyclin-dependent kinases-2 (CDK2) by western blotting in the presence of active compound. In addition, molecular docking revealed that benzo[h]quinolines can correctly dock into the hydrophobic pocket of the targets receptor protein aromatase and CDK2, while their bioavailability/drug-likeness was predicted to be acceptable but requires future optimization. These findings reveal that benzo[h]quinolines act as anti-cancer agents by inducing oxidative stress-mediated DNA damage.

Indexed as

Antineoplastic AgentsApoptosisCell Line, TumorCell ProliferationCyclin-Dependent KinasesDNA DamageHCT116 CellsHumansMCF-7 CellsMolecular Docking SimulationNeoplasmsOxidative StressQuinolinesAntineoplastic AgentsCyclin-Dependent KinasesQuinolines

Identifiers

PMID27922047
PMCPMC5138627
OpenAlexW2560455910

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.