Evidence map›Paper›PMID 21357384›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2011

Polymorphisms in the TNF-α and IL10 gene promoters and risk of arsenic-induced skin lesions and other nondermatological health effects.

Nilanjana Banerjee, Sujay Nandy, James K Kearns, Apurba K Bandyopadhyay, Jayanta K Das, Papiya Majumder, Santanu Basu, Saptarshi Banerjee, Tanmoy Jyoti Sau, J Christopher States and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2011. 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
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

16 citing papers in PubMed, 63 citations in OpenAlex.

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  7. Individual susceptibility to arsenic-induced diseases: the role of host genetics, nutritional status, and the gut microbiome.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Review
  8. Article
  9. Genetic susceptibility to arsenic-induced skin lesions and health effects: a review.Genes and environment : the official journal of the Japanese Environmental Mutagen Society · 2015
    Review
  10. Article
  11. Article
  12. 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

11 authors at 7 institutions in 2 countries.

Nilanjana BanerjeeMolecular and Human Genetics Division, Indian Institute of Chemical Biology (Unit of Council of Scientific and Industrial Research), West Bengal, Kolkata 700032, India.
Sujay Nandy
James K Kearns
Apurba K Bandyopadhyay
Jayanta K Das
Papiya Majumder
Santanu Basu
Saptarshi Banerjee
Tanmoy Jyoti Sau
J Christopher States
Ashok K Giri
Council of Scientific and Industrial Research · INCalcutta National Medical College and Hospital · INMedical College and Hospital, Kolkata · INRamakrishna Mission Vidyamandira · INUniversity of Louisville · USUniversity of Massachusetts Amherst · USWest Bengal University of Health Sciences · IN

Funding

Strategic Vision & Impact on Environmental HealthP30ES014443 · NIEHS · UNIVERSITY OF LOUISVILLE · PI RAMOS, KENNETH S. · 2007 to 2010
$4.4M
RESEARCH/TRAINING IN ENVIRONMENTAL/OCCUPATIONAL HEALTHD43TW000815 · FIC · UNIVERSITY OF CALIFORNIA BERKELEY · PI SMITH, ALLAN H · 1996 to 2011
$2.3M
Arsenic Induced Miotic Arrest Associated ApoptosisR01ES011314 · NIEHS · UNIVERSITY OF LOUISVILLE · PI STATES, J CHRISTOPHER · 2003 to 2009
$1.4M
FIC NIH HHS D43 TW000815NIEHS NIH HHS ES011314NIEHS NIH HHS ES014443
6 · The paper itself

Abstract

In West Bengal, India, at present, more than 26 million people are exposed to arsenic through drinking water. Among them, only 15-20% manifest arsenic-induced noncancerous, precancerous, and cancerous skin lesions, indicating that genetic variants play important role in arsenic susceptibility. Chronic arsenic exposure has been associated with impairment of immune systems in the exposed individuals. Because cytokines are important immune mediators, alteration in expression of these gene products may lead to arsenic-specific disease manifestations. The aim of the present work was to investigate the association between the TNF-α-308G>A (rs1800629) and IL10 -3575T>A (rs1800890) polymorphisms and arsenic-induced dermatological and nondermatological health outcomes. A case-control study was conducted in West Bengal, India, involving 207 cases with arsenic-induced skin lesions and 190 controls without skin lesions having similar arsenic exposure. The polymorphisms were determined using conventional PCR-sequencing method. ELISA was done to determine the serum levels of the two cytokines tumor necrosis factor α (TNF-α) and interleukin 10 (IL10). Associations between the polymorphisms studied and nondermatological health effects in the study subjects were determined from our epidemiological survey data. Individuals with GA/AA (-308 TNF-α) and TA/AA (-3575 IL10) genotypes were at higher risk of developing arsenic-induced skin lesions, ocular, and respiratory diseases. Also the -308 TNF A allele corresponded to a higher production of TNF-α, and -3575 IL10 A allele corresponded to a lower production of IL10. Thus, the polymorphisms studied impart significant risk toward development of arsenic-induced dermatological and nondermatological health effects in the chronically exposed population of West Bengal, India.

Indexed as

Polymorphism, GeneticPromoter Regions, GeneticAdolescentAdultAgedArsenicBase SequenceDNA PrimersEnzyme-Linked Immunosorbent AssayFemaleHumansInterleukin-10MaleMiddle AgedPolymerase Chain ReactionSkin DiseasesArsenicDNA PrimersInterleukin-10Tumor Necrosis Factor-alpha

Identifiers

PMID21357384
PMCPMC3115675
OpenAlexW2100266340

What OpenQuestion holds

Textmetadata
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.