Evidence map›Paper›PMID 27068577›Full record

ArticleScientific reports2016

Quercetin, a Natural Flavonoid Interacts with DNA, Arrests Cell Cycle and Causes Tumor Regression by Activating Mitochondrial Pathway of Apoptosis.

Shikha Srivastava, Ranganatha R Somasagara, Mahesh Hegde, Mayilaadumveettil Nishana, Satish Kumar Tadi, Mrinal Srivastava, Bibha Choudhary, Sathees C Raghavan

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 185 papers.

0numbers the graph read from it
0cells of the map it votes in
185citing papers in PubMed
36.2field-weighted citation impact, top 1% 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

185 citing papers in PubMed, 478 citations in OpenAlex.

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  19. Alaska's Flora as a Treatment for Cancer.International journal of biopharmaceutical sciences · 2024
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125 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

8 authors at 2 institutions in 1 country.

Shikha SrivastavaDepartment of Biochemistry, Indian Institute of Science, Bangalore-560 012, India.
Ranganatha R SomasagaraDepartment of Biochemistry, Indian Institute of Science, Bangalore-560 012, India.
Mahesh HegdeDepartment of Biochemistry, Indian Institute of Science, Bangalore-560 012, India.
Mayilaadumveettil NishanaDepartment of Biochemistry, Indian Institute of Science, Bangalore-560 012, India.
Satish Kumar TadiDepartment of Biochemistry, Indian Institute of Science, Bangalore-560 012, India.
Mrinal SrivastavaDepartment of Biochemistry, Indian Institute of Science, Bangalore-560 012, India.
Bibha ChoudharyInstitute of Bioinformatics and Applied Biotechnology, Electronics City, Bangalore 560 100, India.
Sathees C RaghavanDepartment of Biochemistry, Indian Institute of Science, Bangalore-560 012, India.
Indian Institute of Science Bangalore · INInstitute of Bioinformatics and Applied Biotechnology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Naturally occurring compounds are considered as attractive candidates for cancer treatment and prevention. Quercetin and ellagic acid are naturally occurring flavonoids abundantly seen in several fruits and vegetables. In the present study, we evaluate and compare antitumor efficacies of quercetin and ellagic acid in animal models and cancer cell lines in a comprehensive manner. We found that quercetin induced cytotoxicity in leukemic cells in a dose-dependent manner, while ellagic acid showed only limited toxicity. Besides leukemic cells, quercetin also induced cytotoxicity in breast cancer cells, however, its effect on normal cells was limited or none. Further, quercetin caused S phase arrest during cell cycle progression in tested cancer cells. Quercetin induced tumor regression in mice at a concentration 3-fold lower than ellagic acid. Importantly, administration of quercetin lead to ~5 fold increase in the life span in tumor bearing mice compared to that of untreated controls. Further, we found that quercetin interacts with DNA directly, and could be one of the mechanisms for inducing apoptosis in both, cancer cell lines and tumor tissues by activating the intrinsic pathway. Thus, our data suggests that quercetin can be further explored for its potential to be used in cancer therapeutics and combination therapy.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell CycleCell Cycle CheckpointsCell Line, TumorDisease Models, AnimalEllagic AcidMiceMitochondriaNeoplasmsQuercetinSurvival AnalysisTreatment OutcomeAntineoplastic AgentsEllagic AcidQuercetin

Identifiers

PMID27068577
PMCPMC4828642
OpenAlexW2339667234

What OpenQuestion holds

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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.