Chromosome-wide aneuploidy study of cultured circulating myeloid progenitor cells from workers occupationally exposed to formaldehyde
Formaldehyde (FA) is an economically important industrial chemical to which millions of people worldwide are exposed environmentally and occupationally. Recently, the International Agency for Cancer Research concluded that there is sufficient evidence that FA causes leukemia, particularly myeloid le...
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Veröffentlicht in: | Carcinogenesis (New York) 2015-01, Vol.36 (1), p.160-167 |
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creator | Lan, Qing Smith, Martyn T Tang, Xiaojiang Guo, Weihong Vermeulen, Roel Ji, Zhiying Hu, Wei Hubbard, Alan E Shen, Min McHale, Cliona M Qiu, Chuangyi Liu, Songwang Reiss, Boris Beane-Freeman, Laura Blair, Aaron Ge, Yichen Xiong, Jun Li, Laiyu Rappaport, Stephen M Huang, Hanlin Rothman, Nathaniel Zhang, Luoping |
description | Formaldehyde (FA) is an economically important industrial chemical to which millions of people worldwide are exposed environmentally and occupationally. Recently, the International Agency for Cancer Research concluded that there is sufficient evidence that FA causes leukemia, particularly myeloid leukemia. To evaluate the biological plausibility of this association, we employed a chromosome-wide aneuploidy study approach, which allows the evaluation of aneuploidy and structural chromosome aberrations (SCAs) of all 24 chromosomes simultaneously, to analyze cultured myeloid progenitor cells from 29 workers exposed to relatively high levels of FA and 23 unexposed controls. We found statistically significant increases in the frequencies of monosomy, trisomy, tetrasomy and SCAs of multiple chromosomes in exposed workers compared with controls, with particularly notable effects for monosomy 1 [P = 6.02E-06, incidence rate ratio (IRR) = 2.31], monosomy 5 (P = 9.01E-06; IRR = 2.24), monosomy 7 (P = 1.57E-05; IRR = 2.17), trisomy 5 (P = 1.98E-05; IRR = 3.40) and SCAs of chromosome 5 (P = 0.024; IRR = 4.15). The detection of increased levels of monosomy 7 and SCAs of chromosome 5 is particularly relevant as they are frequently observed in acute myeloid leukemia. Our findings provide further evidence that leukemia-related cytogenetic changes can occur in the circulating myeloid progenitor cells of healthy workers exposed to FA, which may be a potential mechanism underlying FA-induced leukemogenesis. |
doi_str_mv | 10.1093/carcin/bgu229 |
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Recently, the International Agency for Cancer Research concluded that there is sufficient evidence that FA causes leukemia, particularly myeloid leukemia. To evaluate the biological plausibility of this association, we employed a chromosome-wide aneuploidy study approach, which allows the evaluation of aneuploidy and structural chromosome aberrations (SCAs) of all 24 chromosomes simultaneously, to analyze cultured myeloid progenitor cells from 29 workers exposed to relatively high levels of FA and 23 unexposed controls. We found statistically significant increases in the frequencies of monosomy, trisomy, tetrasomy and SCAs of multiple chromosomes in exposed workers compared with controls, with particularly notable effects for monosomy 1 [P = 6.02E-06, incidence rate ratio (IRR) = 2.31], monosomy 5 (P = 9.01E-06; IRR = 2.24), monosomy 7 (P = 1.57E-05; IRR = 2.17), trisomy 5 (P = 1.98E-05; IRR = 3.40) and SCAs of chromosome 5 (P = 0.024; IRR = 4.15). The detection of increased levels of monosomy 7 and SCAs of chromosome 5 is particularly relevant as they are frequently observed in acute myeloid leukemia. Our findings provide further evidence that leukemia-related cytogenetic changes can occur in the circulating myeloid progenitor cells of healthy workers exposed to FA, which may be a potential mechanism underlying FA-induced leukemogenesis.</description><identifier>ISSN: 0143-3334</identifier><identifier>EISSN: 1460-2180</identifier><identifier>DOI: 10.1093/carcin/bgu229</identifier><identifier>PMID: 25391402</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Adult ; Aneuploidy ; Case-Control Studies ; Cells, Cultured ; Chromosomes, Human - drug effects ; Cross-Sectional Studies ; Disinfectants - adverse effects ; Female ; Follow-Up Studies ; Formaldehyde - adverse effects ; Humans ; In Situ Hybridization, Fluorescence ; Male ; Myeloid Progenitor Cells - drug effects ; Myeloid Progenitor Cells - metabolism ; Myeloid Progenitor Cells - pathology ; Occupational Exposure - adverse effects ; Original Manuscript ; Prognosis</subject><ispartof>Carcinogenesis (New York), 2015-01, Vol.36 (1), p.160-167</ispartof><rights>Published by Oxford University Press 2014.</rights><rights>Published by Oxford University Press 2014. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c453t-a6297cec48309dbcc73e89a932cd9fba1239a99ab4de9cc7a6d9816802f9c7b73</citedby><cites>FETCH-LOGICAL-c453t-a6297cec48309dbcc73e89a932cd9fba1239a99ab4de9cc7a6d9816802f9c7b73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25391402$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lan, Qing</creatorcontrib><creatorcontrib>Smith, Martyn T</creatorcontrib><creatorcontrib>Tang, Xiaojiang</creatorcontrib><creatorcontrib>Guo, Weihong</creatorcontrib><creatorcontrib>Vermeulen, Roel</creatorcontrib><creatorcontrib>Ji, Zhiying</creatorcontrib><creatorcontrib>Hu, Wei</creatorcontrib><creatorcontrib>Hubbard, Alan E</creatorcontrib><creatorcontrib>Shen, Min</creatorcontrib><creatorcontrib>McHale, Cliona M</creatorcontrib><creatorcontrib>Qiu, Chuangyi</creatorcontrib><creatorcontrib>Liu, Songwang</creatorcontrib><creatorcontrib>Reiss, Boris</creatorcontrib><creatorcontrib>Beane-Freeman, Laura</creatorcontrib><creatorcontrib>Blair, Aaron</creatorcontrib><creatorcontrib>Ge, Yichen</creatorcontrib><creatorcontrib>Xiong, Jun</creatorcontrib><creatorcontrib>Li, Laiyu</creatorcontrib><creatorcontrib>Rappaport, Stephen M</creatorcontrib><creatorcontrib>Huang, Hanlin</creatorcontrib><creatorcontrib>Rothman, Nathaniel</creatorcontrib><creatorcontrib>Zhang, Luoping</creatorcontrib><title>Chromosome-wide aneuploidy study of cultured circulating myeloid progenitor cells from workers occupationally exposed to formaldehyde</title><title>Carcinogenesis (New York)</title><addtitle>Carcinogenesis</addtitle><description>Formaldehyde (FA) is an economically important industrial chemical to which millions of people worldwide are exposed environmentally and occupationally. Recently, the International Agency for Cancer Research concluded that there is sufficient evidence that FA causes leukemia, particularly myeloid leukemia. To evaluate the biological plausibility of this association, we employed a chromosome-wide aneuploidy study approach, which allows the evaluation of aneuploidy and structural chromosome aberrations (SCAs) of all 24 chromosomes simultaneously, to analyze cultured myeloid progenitor cells from 29 workers exposed to relatively high levels of FA and 23 unexposed controls. We found statistically significant increases in the frequencies of monosomy, trisomy, tetrasomy and SCAs of multiple chromosomes in exposed workers compared with controls, with particularly notable effects for monosomy 1 [P = 6.02E-06, incidence rate ratio (IRR) = 2.31], monosomy 5 (P = 9.01E-06; IRR = 2.24), monosomy 7 (P = 1.57E-05; IRR = 2.17), trisomy 5 (P = 1.98E-05; IRR = 3.40) and SCAs of chromosome 5 (P = 0.024; IRR = 4.15). The detection of increased levels of monosomy 7 and SCAs of chromosome 5 is particularly relevant as they are frequently observed in acute myeloid leukemia. Our findings provide further evidence that leukemia-related cytogenetic changes can occur in the circulating myeloid progenitor cells of healthy workers exposed to FA, which may be a potential mechanism underlying FA-induced leukemogenesis.</description><subject>Adult</subject><subject>Aneuploidy</subject><subject>Case-Control Studies</subject><subject>Cells, Cultured</subject><subject>Chromosomes, Human - drug effects</subject><subject>Cross-Sectional Studies</subject><subject>Disinfectants - adverse effects</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Formaldehyde - adverse effects</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Male</subject><subject>Myeloid Progenitor Cells - drug effects</subject><subject>Myeloid Progenitor Cells - metabolism</subject><subject>Myeloid Progenitor Cells - pathology</subject><subject>Occupational Exposure - adverse effects</subject><subject>Original Manuscript</subject><subject>Prognosis</subject><issn>0143-3334</issn><issn>1460-2180</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkctOwzAQRS0EglJYskX-gYBfTeMNEqp4SZXYwDpy7ElrcOLITij5AP4bV4UKNvPQvXNmcRG6oOSKEsmvtQrattfVamBMHqAJFTnJGC3IIZoQKnjGORcn6DTGN0JozmfyGJ2wGZdUEDZBX4t18I2PvoFsYw1g1cLQOW_NiGM_pOprrAfXDwEM1jakWfW2XeFmhK0Nd8GvoLW9D1iDcxHXCYg3PrxDiNhrPXTpwLfKuRHDZ-djAvUe1z40yhlYjwbO0FGtXITznz5Fr_d3L4vHbPn88LS4XWZazHifqZzJuQYtCk6kqbSecyikkpxpI-tKUcbTJlUlDMikqtzIguYFYbXU82rOp-hmx-2GqgGjoe2DcmUXbKPCWHply_9Ka9flyn-UgklKhEyAbAfQwccYoN7fUlJu8yh3eZS7PJL_8u_Dvfs3AP4Nu-mPsw</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Lan, Qing</creator><creator>Smith, Martyn T</creator><creator>Tang, Xiaojiang</creator><creator>Guo, Weihong</creator><creator>Vermeulen, Roel</creator><creator>Ji, Zhiying</creator><creator>Hu, Wei</creator><creator>Hubbard, Alan E</creator><creator>Shen, Min</creator><creator>McHale, Cliona M</creator><creator>Qiu, Chuangyi</creator><creator>Liu, Songwang</creator><creator>Reiss, Boris</creator><creator>Beane-Freeman, Laura</creator><creator>Blair, Aaron</creator><creator>Ge, Yichen</creator><creator>Xiong, Jun</creator><creator>Li, Laiyu</creator><creator>Rappaport, Stephen M</creator><creator>Huang, Hanlin</creator><creator>Rothman, Nathaniel</creator><creator>Zhang, Luoping</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20150101</creationdate><title>Chromosome-wide aneuploidy study of cultured circulating myeloid progenitor cells from workers occupationally exposed to formaldehyde</title><author>Lan, Qing ; Smith, Martyn T ; Tang, Xiaojiang ; Guo, Weihong ; Vermeulen, Roel ; Ji, Zhiying ; Hu, Wei ; Hubbard, Alan E ; Shen, Min ; McHale, Cliona M ; Qiu, Chuangyi ; Liu, Songwang ; Reiss, Boris ; Beane-Freeman, Laura ; Blair, Aaron ; Ge, Yichen ; Xiong, Jun ; Li, Laiyu ; Rappaport, Stephen M ; Huang, Hanlin ; Rothman, Nathaniel ; Zhang, Luoping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c453t-a6297cec48309dbcc73e89a932cd9fba1239a99ab4de9cc7a6d9816802f9c7b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Aneuploidy</topic><topic>Case-Control Studies</topic><topic>Cells, Cultured</topic><topic>Chromosomes, Human - drug effects</topic><topic>Cross-Sectional Studies</topic><topic>Disinfectants - adverse effects</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Formaldehyde - adverse effects</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Male</topic><topic>Myeloid Progenitor Cells - drug effects</topic><topic>Myeloid Progenitor Cells - metabolism</topic><topic>Myeloid Progenitor Cells - pathology</topic><topic>Occupational Exposure - adverse effects</topic><topic>Original Manuscript</topic><topic>Prognosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lan, Qing</creatorcontrib><creatorcontrib>Smith, Martyn T</creatorcontrib><creatorcontrib>Tang, Xiaojiang</creatorcontrib><creatorcontrib>Guo, Weihong</creatorcontrib><creatorcontrib>Vermeulen, Roel</creatorcontrib><creatorcontrib>Ji, Zhiying</creatorcontrib><creatorcontrib>Hu, Wei</creatorcontrib><creatorcontrib>Hubbard, Alan E</creatorcontrib><creatorcontrib>Shen, Min</creatorcontrib><creatorcontrib>McHale, Cliona M</creatorcontrib><creatorcontrib>Qiu, Chuangyi</creatorcontrib><creatorcontrib>Liu, Songwang</creatorcontrib><creatorcontrib>Reiss, Boris</creatorcontrib><creatorcontrib>Beane-Freeman, Laura</creatorcontrib><creatorcontrib>Blair, Aaron</creatorcontrib><creatorcontrib>Ge, Yichen</creatorcontrib><creatorcontrib>Xiong, Jun</creatorcontrib><creatorcontrib>Li, Laiyu</creatorcontrib><creatorcontrib>Rappaport, Stephen M</creatorcontrib><creatorcontrib>Huang, Hanlin</creatorcontrib><creatorcontrib>Rothman, Nathaniel</creatorcontrib><creatorcontrib>Zhang, Luoping</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Carcinogenesis (New York)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lan, Qing</au><au>Smith, Martyn T</au><au>Tang, Xiaojiang</au><au>Guo, Weihong</au><au>Vermeulen, Roel</au><au>Ji, Zhiying</au><au>Hu, Wei</au><au>Hubbard, Alan E</au><au>Shen, Min</au><au>McHale, Cliona M</au><au>Qiu, Chuangyi</au><au>Liu, Songwang</au><au>Reiss, Boris</au><au>Beane-Freeman, Laura</au><au>Blair, Aaron</au><au>Ge, Yichen</au><au>Xiong, Jun</au><au>Li, Laiyu</au><au>Rappaport, Stephen M</au><au>Huang, Hanlin</au><au>Rothman, Nathaniel</au><au>Zhang, Luoping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chromosome-wide aneuploidy study of cultured circulating myeloid progenitor cells from workers occupationally exposed to formaldehyde</atitle><jtitle>Carcinogenesis (New York)</jtitle><addtitle>Carcinogenesis</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>36</volume><issue>1</issue><spage>160</spage><epage>167</epage><pages>160-167</pages><issn>0143-3334</issn><eissn>1460-2180</eissn><abstract>Formaldehyde (FA) is an economically important industrial chemical to which millions of people worldwide are exposed environmentally and occupationally. Recently, the International Agency for Cancer Research concluded that there is sufficient evidence that FA causes leukemia, particularly myeloid leukemia. To evaluate the biological plausibility of this association, we employed a chromosome-wide aneuploidy study approach, which allows the evaluation of aneuploidy and structural chromosome aberrations (SCAs) of all 24 chromosomes simultaneously, to analyze cultured myeloid progenitor cells from 29 workers exposed to relatively high levels of FA and 23 unexposed controls. We found statistically significant increases in the frequencies of monosomy, trisomy, tetrasomy and SCAs of multiple chromosomes in exposed workers compared with controls, with particularly notable effects for monosomy 1 [P = 6.02E-06, incidence rate ratio (IRR) = 2.31], monosomy 5 (P = 9.01E-06; IRR = 2.24), monosomy 7 (P = 1.57E-05; IRR = 2.17), trisomy 5 (P = 1.98E-05; IRR = 3.40) and SCAs of chromosome 5 (P = 0.024; IRR = 4.15). The detection of increased levels of monosomy 7 and SCAs of chromosome 5 is particularly relevant as they are frequently observed in acute myeloid leukemia. Our findings provide further evidence that leukemia-related cytogenetic changes can occur in the circulating myeloid progenitor cells of healthy workers exposed to FA, which may be a potential mechanism underlying FA-induced leukemogenesis.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>25391402</pmid><doi>10.1093/carcin/bgu229</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Adult Aneuploidy Case-Control Studies Cells, Cultured Chromosomes, Human - drug effects Cross-Sectional Studies Disinfectants - adverse effects Female Follow-Up Studies Formaldehyde - adverse effects Humans In Situ Hybridization, Fluorescence Male Myeloid Progenitor Cells - drug effects Myeloid Progenitor Cells - metabolism Myeloid Progenitor Cells - pathology Occupational Exposure - adverse effects Original Manuscript Prognosis |
title | Chromosome-wide aneuploidy study of cultured circulating myeloid progenitor cells from workers occupationally exposed to formaldehyde |
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