Evidence map›Paper›PMID 28881718›Full record

ArticleOncotarget2017

Quercetin inhibits Cr(VI)-induced malignant cell transformation by targeting miR-21-PDCD4 signaling pathway.

Poyil Pratheeshkumar, Young-Ok Son, Sasidharan Padmaja Divya, Lei Wang, Lilia Turcios, Ram Vinod Roy, John Andrew Hitron, Donghern Kim, Jin Dai, Padmaja Asha and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.0field-weighted citation impact, top 4% 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

34 citing papers in PubMed, 73 citations in OpenAlex.

  1. Review
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  8. Article
  9. Recent Advances in Potential Health Benefits of Quercetin.Pharmaceuticals (Basel, Switzerland) · 2023
    Review
  10. Review
  11. Epigenetic and epitranscriptomic mechanisms of chromium carcinogenesis.Advances in pharmacology (San Diego, Calif.) · 2023
    Article
  12. Review
  13. Review
  14. Article
  15. 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

12 authors at 2 institutions in 2 countries.

Poyil Pratheeshkumar *Center for Research on Environmental Disease, University of Kentucky, Lexington, KY, USA.
Young-Ok Son *Center for Research on Environmental Disease, University of Kentucky, Lexington, KY, USA.
Sasidharan Padmaja DivyaCenter for Research on Environmental Disease, University of Kentucky, Lexington, KY, USA.
Lei WangCenter for Research on Environmental Disease, University of Kentucky, Lexington, KY, USA.
Lilia TurciosDepartment of Surgery, University of Kentucky, College of Medicine, Lexington, KY, USA.
Ram Vinod RoyCenter for Research on Environmental Disease, University of Kentucky, Lexington, KY, USA.
John Andrew HitronCenter for Research on Environmental Disease, University of Kentucky, Lexington, KY, USA.
Donghern KimDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, USA.
Jin DaiDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, USA.
Padmaja AshaNational Centre for Aquatic Animal Health, Cochin University of Science and Technology, Cochin, India.
Zhuo ZhangDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, USA.
Xianglin ShiCenter for Research on Environmental Disease, University of Kentucky, Lexington, KY, USA.
University of Kentucky · USCochin University of Science and Technology · IN

Funding

TRAINING GRANT IN MOLECULAR MECHANISMS OF TOXICITY.T32ES007266 · NIEHS · UNIVERSITY OF KENTUCKY · PI LIU, XIAOQI, MELLON, ISABEL W · 1990 to 2020
$3.7M
Oxidative stress, Cr(VI) carcinogenesis, and preventionR01ES025515 · NIEHS · UNIVERSITY OF KENTUCKY · PI SHI, XIANGLIN, ZHANG, ZHUO · 2015 to 2019
$2.9M
Prevention of UV-induced carcinogenesis by cyanidin-3-glucosideR01ES017244 · NIEHS · UNIVERSITY OF KENTUCKY · PI SHI, XIANGLIN · 2011 to 2015
$1.7M
NIEHS NIH HHS R01 ES017244NIEHS NIH HHS R01 ES025515NIEHS NIH HHS T32 ES007266
6 · The paper itself

Abstract

Hexavalent chromium [Cr(VI)] is an important human carcinogen associated with pulmonary diseases and lung cancer. Inhibition of Cr(VI)-induced carcinogenesis by a dietary antioxidant is a novel approach. Quercetin is one of the most abundant dietary flavonoids widely present in many fruits and vegetables, possesses potent antioxidant and anticancer properties. MicroRNA-21 (miR-21) is a key oncomiR significantly elevated in the majority of human cancers that exerts its oncogenic activity by targeting the tumor suppressor gene programmed cell death 4 (PDCD4). The present study examined the effect of quercetin on the inhibition of Cr(VI)-induced malignant cell transformation and the role of miR-21-PDCD4 signaling involved. Our results showed that quercetin decreased ROS generation induced by Cr(VI) exposure in BEAS-2B cells. Chronic Cr(VI) exposure induced malignant cell transformation, increased miR-21 expression and caused inhibition of PDCD4, which were significantly inhibited by the treatment of quercetin in a dose dependent manner. Nude mice injected with BEAS-2B cells chronically exposed to Cr(VI) in the presence of quercetin showed reduced tumor incidence compared to Cr(VI) alone treated group. Stable knockdown of miR-21 and overexpression of PDCD4 or catalase in BEAS-2B cells suppressed Cr(VI)-induced malignant transformation and tumorigenesis. Taken together, these results demonstrate that quercetin is able to protect BEAS-2B cells from Cr(VI)-induced carcinogenesis by targeting miR-21-PDCD4 signaling.

Indexed as

hexavalent chromiummalignant cell transformationmiR-21-PDCD4 signalingquercetinROS

Identifiers

PMID28881718
PMCPMC5581017
OpenAlexW2438335097

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.