Matches in SemOpenAlex for { <https://semopenalex.org/work/W2912777592> ?p ?o ?g. }
- W2912777592 endingPage "36" @default.
- W2912777592 startingPage "24" @default.
- W2912777592 abstract "To characterize the impact of PCB exposure on DNA methylation in peripheral blood leucocytes and to evaluate the corresponding changes in relation to possible health effects, with a focus on B-cell lymphoma.We conducted an epigenome-wide association study on 611 adults free of diagnosed disease, living in Italy and Sweden, in whom we also measured plasma concentrations of 6 PCB congeners, DDE and hexachlorobenzene.We identified 650 CpG sites whose methylation correlates strongly (FDR < 0.01) with plasma concentrations of at least one PCB congener. Stronger effects were observed in males and in Sweden. This epigenetic exposure profile shows extensive and highly statistically significant overlaps with published profiles associated with the risk of future B-cell chronic lymphocytic leukemia (CLL) as well as with clinical CLL (38 and 28 CpG sites, respectively). For all these sites, the methylation changes were in the same direction for increasing exposure and for higher disease risk or clinical disease status, suggesting an etiological link between exposure and CLL. Mediation analysis reinforced the suggestion of a causal link between exposure, changes in DNA methylation and disease. Disease connectivity analysis identified multiple additional diseases associated with differentially methylated genes, including melanoma for which an etiological link with PCB exposure is established, as well as developmental and neurological diseases for which there is corresponding epidemiological evidence. Differentially methylated genes include many homeobox genes, suggesting that PCBs target stem cells. Furthermore, numerous polycomb protein target genes were hypermethylated with increasing exposure, an effect known to constitute an early marker of carcinogenesis.This study provides mechanistic evidence in support of a link between exposure to PCBs and the etiology of CLL and underlines the utility of omic profiling in the evaluation of the potential toxicity of environmental chemicals." @default.
- W2912777592 created "2019-02-21" @default.
- W2912777592 creator A5013532520 @default.
- W2912777592 creator A5018186238 @default.
- W2912777592 creator A5026704231 @default.
- W2912777592 creator A5031468653 @default.
- W2912777592 creator A5038579481 @default.
- W2912777592 creator A5045120834 @default.
- W2912777592 creator A5054577207 @default.
- W2912777592 creator A5055284074 @default.
- W2912777592 creator A5057049990 @default.
- W2912777592 creator A5064532620 @default.
- W2912777592 creator A5071637943 @default.
- W2912777592 creator A5076619800 @default.
- W2912777592 creator A5081219595 @default.
- W2912777592 creator A5083218466 @default.
- W2912777592 creator A5085715708 @default.
- W2912777592 creator A5089625312 @default.
- W2912777592 date "2019-05-01" @default.
- W2912777592 modified "2023-09-27" @default.
- W2912777592 title "DNA methylation profiling implicates exposure to PCBs in the pathogenesis of B-cell chronic lymphocytic leukemia" @default.
- W2912777592 cites W1605195795 @default.
- W2912777592 cites W1728875604 @default.
- W2912777592 cites W1908991493 @default.
- W2912777592 cites W1978295003 @default.
- W2912777592 cites W1979073669 @default.
- W2912777592 cites W1979187574 @default.
- W2912777592 cites W1983262171 @default.
- W2912777592 cites W1986560938 @default.
- W2912777592 cites W1992081826 @default.
- W2912777592 cites W1992770688 @default.
- W2912777592 cites W2012480853 @default.
- W2912777592 cites W2022115167 @default.
- W2912777592 cites W2026252313 @default.
- W2912777592 cites W2028029749 @default.
- W2912777592 cites W2029634407 @default.
- W2912777592 cites W2029742174 @default.
- W2912777592 cites W2030545670 @default.
- W2912777592 cites W2031319416 @default.
- W2912777592 cites W2042087070 @default.
- W2912777592 cites W2043422388 @default.
- W2912777592 cites W2046746600 @default.
- W2912777592 cites W2049422251 @default.
- W2912777592 cites W2073449334 @default.
- W2912777592 cites W2074932610 @default.
- W2912777592 cites W2077502047 @default.
- W2912777592 cites W2084599100 @default.
- W2912777592 cites W2086232624 @default.
- W2912777592 cites W2086603645 @default.
- W2912777592 cites W2087008478 @default.
- W2912777592 cites W2094065712 @default.
- W2912777592 cites W2099892743 @default.
- W2912777592 cites W2100519706 @default.
- W2912777592 cites W2115715088 @default.
- W2912777592 cites W2138737838 @default.
- W2912777592 cites W2139565721 @default.
- W2912777592 cites W2152633679 @default.
- W2912777592 cites W2153424791 @default.
- W2912777592 cites W2158532144 @default.
- W2912777592 cites W2161841622 @default.
- W2912777592 cites W2167021978 @default.
- W2912777592 cites W2169556367 @default.
- W2912777592 cites W2189866696 @default.
- W2912777592 cites W2192064401 @default.
- W2912777592 cites W2221346445 @default.
- W2912777592 cites W2299377942 @default.
- W2912777592 cites W2363899809 @default.
- W2912777592 cites W2398852852 @default.
- W2912777592 cites W2437450654 @default.
- W2912777592 cites W2503385401 @default.
- W2912777592 cites W2529448842 @default.
- W2912777592 cites W2543905218 @default.
- W2912777592 cites W2546844804 @default.
- W2912777592 cites W2553776432 @default.
- W2912777592 cites W2586380847 @default.
- W2912777592 cites W2590278769 @default.
- W2912777592 cites W2593892347 @default.
- W2912777592 cites W2601117488 @default.
- W2912777592 cites W2608446199 @default.
- W2912777592 cites W2612120761 @default.
- W2912777592 cites W2613929178 @default.
- W2912777592 cites W2724632208 @default.
- W2912777592 cites W2748253088 @default.
- W2912777592 cites W2755260711 @default.
- W2912777592 cites W2762864566 @default.
- W2912777592 cites W2769208514 @default.
- W2912777592 cites W2789727733 @default.
- W2912777592 cites W2790275459 @default.
- W2912777592 cites W4232037809 @default.
- W2912777592 doi "https://doi.org/10.1016/j.envint.2019.01.068" @default.
- W2912777592 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7063446" @default.
- W2912777592 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30776747" @default.
- W2912777592 hasPublicationYear "2019" @default.
- W2912777592 type Work @default.
- W2912777592 sameAs 2912777592 @default.
- W2912777592 citedByCount "21" @default.
- W2912777592 countsByYear W29127775922019 @default.
- W2912777592 countsByYear W29127775922020 @default.