Evidence map›Paper›PMID 33340130›Full record

ArticleJournal of applied toxicology : JAT2021

Association between the polymorphism of three genes involved in the methylation and efflux of arsenic (As3MT, MRP1, and P-gp) with lung cancer in a Mexican cohort.

Rogelio Recio-Vega, Sandra Hernandez-Gonzalez, Gladis Michel-Ramirez, Edgar Olivas-Calderón, R Clark Lantz, A Jay Gandolfi, Mary Kay Amistadi

Open access · greenAbstract read
In one paragraph

Article in Journal of applied toxicology : JAT, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
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

7 authors at 3 institutions in 2 countries.

Rogelio Recio-VegaDepartment of Environmental Health, Biomedical Research Center, School of Medicine, University of Coahuila, Torreon, Coahuila, Mexico.ORCID 0000-0002-5976-6516
Sandra Hernandez-GonzalezSchool of Chemical Sciences, University Juarez of Durango, Gomez Palacio, Durango, Mexico.
Gladis Michel-RamirezDepartment of Environmental Health, Biomedical Research Center, School of Medicine, University of Coahuila, Torreon, Coahuila, Mexico.
Edgar Olivas-CalderónDepartment of Environmental Health, Biomedical Research Center, School of Medicine, University of Coahuila, Torreon, Coahuila, Mexico.
R Clark LantzSouthwest Environmental Health Science Center, University of Arizona, Tucson, Arizona, USA.
A Jay GandolfiSouthwest Environmental Health Science Center, University of Arizona, Tucson, Arizona, USA.
Mary Kay AmistadiDepartment of Soil, Water and Environmental Science, University of Arizona, Tucson, Arizona, USA.
Universidad Autónoma de Coahuila · MXUniversity of Arizona · USUniversidad Juárez del Estado de Durango · MX

Funding

TRANSPORT OF TRACE METALS IN A POLLUTED AQUIFERP42ES004940 · NIEHS · UNIVERSITY OF ARIZONA · PI Jon D Chorover · 1990 to 2026
$68.1M
SOUTHWEST ENVIRONMENTAL HEALTH SCIENCES CENTERP30ES006694 · NIEHS · UNIVERSITY OF ARIZONA · PI DEAN BILLHEIMER · 1994 to 2026
$36.7M
NIEHS NIH HHS P30 ES006694NIEHS NIH HHS P42 ES004940
6 · The paper itself

Abstract

Lung cancer is the most common neoplasm and the primary cause-related mortality in developed and in most of nondeveloped countries. Epidemiological studies have demonstrated that even at low arsenic doses, the lungs are one of the main target organs and that chronic arsenic exposure has been associated with an increase in lung cancer development. Among the risk factors for cancer, arsenic methylation efficiency (As3MT) and the clearance of arsenic from cells by two members of the ATP-binding cassette (ABC) transporter family (multidrug resistance protein 1 [MRP1] and P-glycoprotein [P-gp]) play an important role in processing of arsenic and decreasing its intracellular levels. This study aimed to evaluate the association between chronic exposure to arsenic with polymorphism of three proteins involved in arsenic metabolism and efflux of the metalloid in subjects with lung cancer. Polymorphism in As3MT, MRP1, and P-gp modified the arsenic metabolism increasing significantly the As

Indexed as

AdultAgedAged, 80 and overArsenicATP-Binding Cassette, Sub-Family C ProteinsATP Binding Cassette Transporter, Subfamily B, Member 1Cohort StudiesCross-Sectional StudiesDrinking WaterEnvironmental ExposureFemaleGenotypeHumansLung NeoplasmsMaleMethylationArsenicAS3MT protein, humanATP-Binding Cassette, Sub-Family C ProteinsATP Binding Cassette Transporter, Subfamily B, Member 1Drinking WaterMethyltransferasesmultidrug resistance-associated protein 1arsenicAs3MTlung cancerMRP1P-gppolymorphism

Identifiers

PMID33340130
PMCPMC8626135
OpenAlexW3114944141

What OpenQuestion holds

Textmetadata
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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.