Evidence map›Paper›PMID 32717274›Full record

ArticleCancer letters2020

Emerging crosstalk between long non-coding RNAs and Nrf2 signaling.

Shamee Bhattacharjee, Jia Li, Roderick H Dashwood

Open access · hybridAbstract read
In one paragraph

Article in Cancer letters, 2020. 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
2.2field-weighted citation impact, top 11% 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, 33 citations in OpenAlex.

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  16. Epigenetic Regulation of NRF2/KEAP1 by Phytochemicals.Antioxidants (Basel, Switzerland) · 2020
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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

3 authors at 1 institution in 2 countries.

Shamee BhattacharjeeWest Bengal State University, Department of Zoology, Kolkata, India; Center for Epigenetics & Disease Prevention, Texas A&M Health Science Center, Houston, TX, USA. Electronic address: shamee.zoology@wbsu.ac.in.
Jia LiCenter for Epigenetics & Disease Prevention, Texas A&M Health Science Center, Houston, TX, USA. Electronic address: jiali@tamu.edu.
Roderick H DashwoodCenter for Epigenetics & Disease Prevention, Texas A&M Health Science Center, Houston, TX, USA; Department of Translational Medical Sciences, Texas A&M College of Medicine, Texas A&M AgriLife, College Station, TX, USA; Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. Electronic address: dashwood@tamu.edu.
Texas A&M Health Science Center · US

Funding

Transplacental Chemoprevention of Lung Tumors and LymphomasP01CA090890 · NCI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI DASHWOOD, RODERICK H · 2003 to 2014
$14.2M
Dietary HDAC Inhibitors in Colon Cancer PreventionR01CA122959 · NCI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI DASHWOOD, RODERICK H · 2008 to 2023
$4.3M
Immunoepigenetic targeting of MHC regulators in FAPR01CA257559 · NCI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI Roderick H Dashwood, Eduardo Vilar Sanchez · 2023 to 2026
$2.3M
NCI NIH HHS P01 CA090890NCI NIH HHS R01 CA122959NCI NIH HHS R01 CA257559
6 · The paper itself

Abstract

Diverse stimuli trigger Nrf2 signaling, which in turn transcriptionally regulates an array of downstream targets, providing for multiple layers of control. While Nrf2 activity largely is governed by posttranslational modification of critical thiol residues in the protein partner and redox sensor Keap1, fine-tuning is provided by additional mechanisms - including epigenetic regulation. Herein, we review the emerging significance of long non-coding RNAs (lncRNA) as downstream targets and upstream regulators of the Nrf2 signaling pathway. Among the ~16000 lncRNAs in GENCODE, some have been validated as transcriptionally regulated by Nrf2 (e.g., LUCAT1, NMRAL2P, ODRUL, ROR and TUG1), and others have been identified as upstream regulators of Nrf2 expression (e.g., HOTAIR, MALAT1, MEG1, NRAL and UCA1). Bioinformatic analyses of annotated human lncRNAs identified putative Nrf2 binding sites in the promoter regions of 13,285 lncRNAs. Further investigation is warranted to validate the many novel lncRNAs as bona fide Nrf2-regulated targets, and their roles in Nrf2 signaling. Nrf2 is considered a promising therapeutic candidate for cancer and other chronic diseases; thus, targeting the associated lncRNAs might provide for a more refined fine-tuning of the system, depending on cellular and pathophysiological context.

Indexed as

Gene Expression RegulationHumansNF-E2-Related Factor 2RNA, Long NoncodingSignal TransductionNFE2L2 protein, humanNF-E2-Related Factor 2RNA, Long NoncodingHOTAIRHypoxiaKeap1MALAT1MEG3Oxidative stress

Identifiers

PMID32717274
PMCPMC12991830
OpenAlexW3044724221

What OpenQuestion holds

Textmetadata
LicenceTDM
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.