Evidence map›Paper›PMID 39995157›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2025

Solvent Exposure, Genetic Susceptibility, and Risk of Bladder Cancer.

Deborah A Tadesse, Nathaniel Rothman, Shuai Xie, Lauren M Hurwitz, Melissa C Friesen, Dalsu Baris, Molly Schwenn, Alison Johnson, Margaret R Karagas, Debra T Silverman and 1 more

Abstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Deborah A TadesseDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.ORCID 0009-0001-2781-1415
Nathaniel RothmanDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.ORCID 0000-0001-6924-0895
Shuai XieDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.ORCID 0000-0002-0426-7613
Lauren M HurwitzDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.ORCID 0000-0001-8932-5028
Melissa C FriesenDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.ORCID 0000-0002-1695-3282
Dalsu BarisDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.ORCID 0009-0001-6520-9249
Molly SchwennRetired, Formerly Maine Cancer Registry, Augusta, Maine.ORCID 0000-0002-9395-4887
Alison JohnsonRetired, Formerly Vermont Department of Health, Burlington, Vermont.ORCID 0000-0002-1113-1191
Margaret R KaragasGeisel School of Medicine at Dartmouth, Hanover, New Hampshire.ORCID 0000-0002-6398-7362
Debra T SilvermanDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.ORCID 0000-0001-8894-0301
Stella KoutrosDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.ORCID 0000-0001-5294-5485

Funding

Cancer Risk and Environmental ExposuresZIACP010125 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI PURDUE, MARK · 2009 to 2025
$41.3M
Intramural NIH HHS Z99 CA999999Intramural NIH HHS ZIA CP010125
6 · The paper itself

Abstract

The New England Bladder Cancer Study has recently reported an increased bladder cancer risk with occupational exposure to mononuclear aromatic organic solvents, including exposure to benzene, toluene, and xylene and their combination BTX. However, the mechanisms by which BTX influence bladder cancer are unclear. In this study, we evaluated the interaction between BTX and genetic markers in known bladder cancer susceptibility loci and in variants shown to impact the metabolism of these solvents. We used multivariate logistic regression to calculate the ORs, 95% confidence intervals, and P values for multiplicative interaction in 1,182 cases and 1,408 controls from a population-based case-control study from New England. Lifetime occupational exposure to benzene, toluene, xylene, and BTX were assessed using occupational histories and exposure-oriented modules in conjunction with a job-exposure matrix. Buccal cells from mouthwash samples were used to conduct genotyping. Subjects with the highest cumulative exposure to benzene and who carried a risk allele in rs72826305 (CASC15) had an increased risk of bladder cancer (OR = 2.56, 95% confidence interval, 1.28-5.12) compared with those never exposed with no risk alleles (P interaction = 0.03). Additional suggestive joint effects with benzene were evident for those carrying genetic risk variants in FGFR3 (P value = 0.01) and GSTT1 (P interaction = 0.007). Bladder cancer risk is higher among those exposed to BTX-containing solvents who also harbor common variants in CASC15, FGFR3, and GSTT1, adding to the evidence of a plausible link between these exposures and bladder cancer risk. Prevention Relevance: Our findings suggest that bladder cancer risk is higher among those exposed to BTX-containing solvents who also harbor common genetic polymorphisms associated with bladder cancer. The joint contribution of genetics and occupational exposures may play an important role in the etiology of bladder cancer.

Indexed as

Genetic Predisposition to DiseaseOccupational ExposureSolventsUrinary Bladder NeoplasmsAdultAgedBenzeneCase-Control StudiesFemaleGenotypeGlutathione TransferaseHumansMaleMiddle AgedPolymorphism, Single NucleotideRisk FactorsBenzeneglutathione S-transferase T1Glutathione TransferaseSolventsToluene

Identifiers

PMID39995157
PMCPMC12045719

What Socratic holds

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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 Socratic graph.