Combined effects of serum trace metals and polymorphisms of CYP1A1 or GSTM1 on non-small cell lung cancer: A hospital based case–control study in China

Abstract Introduction : The limited information for effects of serum trace elements and genetic polymorphisms on lung cancer is available. Based on a hospital based case–control study, the epidemiological questionnaires were completed by face to face interview, and the gene polymorphisms were tested...

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Veröffentlicht in:Cancer epidemiology 2011-04, Vol.35 (2), p.182-187
Hauptverfasser: Jin, Yongtang, Zhang, Chenye, Xu, Heyun, Xue, Shaoli, Wang, Yasong, Hou, Yong, Kong, Yunming, Xu, Yingchun
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container_end_page 187
container_issue 2
container_start_page 182
container_title Cancer epidemiology
container_volume 35
creator Jin, Yongtang
Zhang, Chenye
Xu, Heyun
Xue, Shaoli
Wang, Yasong
Hou, Yong
Kong, Yunming
Xu, Yingchun
description Abstract Introduction : The limited information for effects of serum trace elements and genetic polymorphisms on lung cancer is available. Based on a hospital based case–control study, the epidemiological questionnaires were completed by face to face interview, and the gene polymorphisms were tested by RFLP–PCR, and serum trace metals were measured by atomic absorption spectrophotometer, and the data was analyzed by the logistic regressive models. Results : The high serum copper level (>1500 ng/ml) or serum copper/zinc ratio (>1) was the risk factors of NSCLC (OR = 3.10, 11.03, respectively), but the ORs of the higher serum Zn (>1200 ng/ml), Se (>50 ng/ml) or Cr3+ (>600 ng/ml) for NSCLC were all significantly less than 0.20 (all p < 0.01) indicating strong protection against NSCLC. While the OR of CYP 1A1 variants carriers with a higher serum Cu or Cu/Zn ratio level was around 3.38 and 12.59, respectively, the risk of CYP1A1 variants carriers with a higher serum Zn is 0.18, Se 0.04 or Cr3+ 0.28. Similarly, compared with the carriers of GSTM1 power with a lower serum Zn, Se or Cr3+ , the OR of the carriers of GSTM1 null with a higher serum Zn, Se and Cr3+ was separately 0.16, 0.07 and 0.26, highlighting the protection against NSCLC. Conclusions : Our findings suggested that CYP1A1 or GSTM1 variants may significantly modify the associations between level of serum trace metals (Cu, Zn, Se or Cr) and NSCLC, indicating the intriguing pathogenesis of lung cancer.
doi_str_mv 10.1016/j.canep.2010.06.004
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Based on a hospital based case–control study, the epidemiological questionnaires were completed by face to face interview, and the gene polymorphisms were tested by RFLP–PCR, and serum trace metals were measured by atomic absorption spectrophotometer, and the data was analyzed by the logistic regressive models. Results : The high serum copper level (&gt;1500 ng/ml) or serum copper/zinc ratio (&gt;1) was the risk factors of NSCLC (OR = 3.10, 11.03, respectively), but the ORs of the higher serum Zn (&gt;1200 ng/ml), Se (&gt;50 ng/ml) or Cr3+ (&gt;600 ng/ml) for NSCLC were all significantly less than 0.20 (all p &lt; 0.01) indicating strong protection against NSCLC. While the OR of CYP 1A1 variants carriers with a higher serum Cu or Cu/Zn ratio level was around 3.38 and 12.59, respectively, the risk of CYP1A1 variants carriers with a higher serum Zn is 0.18, Se 0.04 or Cr3+ 0.28. Similarly, compared with the carriers of GSTM1 power with a lower serum Zn, Se or Cr3+ , the OR of the carriers of GSTM1 null with a higher serum Zn, Se and Cr3+ was separately 0.16, 0.07 and 0.26, highlighting the protection against NSCLC. Conclusions : Our findings suggested that CYP1A1 or GSTM1 variants may significantly modify the associations between level of serum trace metals (Cu, Zn, Se or Cr) and NSCLC, indicating the intriguing pathogenesis of lung cancer.</description><identifier>ISSN: 1877-7821</identifier><identifier>EISSN: 1877-783X</identifier><identifier>DOI: 10.1016/j.canep.2010.06.004</identifier><identifier>PMID: 20638923</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Cancer ; Carcinoma, Non-Small-Cell Lung - blood ; Carcinoma, Non-Small-Cell Lung - enzymology ; Carcinoma, Non-Small-Cell Lung - genetics ; Case-Control Studies ; China - epidemiology ; Combined effect ; Cytochrome P-450 CYP1A1 - genetics ; Epidemiology ; Female ; Gene polymorphism ; Genetic Predisposition to Disease ; Glutathione Transferase - genetics ; Hematology, Oncology and Palliative Medicine ; Humans ; Internal Medicine ; Lung cancer ; Male ; Metals ; Middle Aged ; Non-small cell lung cancer (NSCLC) ; Risk Factors ; Serum trace metal ; Smoking ; Studies ; Trace elements ; Trace Elements - blood</subject><ispartof>Cancer epidemiology, 2011-04, Vol.35 (2), p.182-187</ispartof><rights>2010</rights><rights>Crown Copyright © 2010. 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All rights reserved.</rights><rights>Copyright Elsevier Limited 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-26f8b441385a55f6968130701fa3bc4507d2ff3f305b0281696a6948015523373</citedby><cites>FETCH-LOGICAL-c441t-26f8b441385a55f6968130701fa3bc4507d2ff3f305b0281696a6948015523373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1032598592?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995,64385,64387,64389,72469</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20638923$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jin, Yongtang</creatorcontrib><creatorcontrib>Zhang, Chenye</creatorcontrib><creatorcontrib>Xu, Heyun</creatorcontrib><creatorcontrib>Xue, Shaoli</creatorcontrib><creatorcontrib>Wang, Yasong</creatorcontrib><creatorcontrib>Hou, Yong</creatorcontrib><creatorcontrib>Kong, Yunming</creatorcontrib><creatorcontrib>Xu, Yingchun</creatorcontrib><title>Combined effects of serum trace metals and polymorphisms of CYP1A1 or GSTM1 on non-small cell lung cancer: A hospital based case–control study in China</title><title>Cancer epidemiology</title><addtitle>Cancer Epidemiol</addtitle><description>Abstract Introduction : The limited information for effects of serum trace elements and genetic polymorphisms on lung cancer is available. Based on a hospital based case–control study, the epidemiological questionnaires were completed by face to face interview, and the gene polymorphisms were tested by RFLP–PCR, and serum trace metals were measured by atomic absorption spectrophotometer, and the data was analyzed by the logistic regressive models. Results : The high serum copper level (&gt;1500 ng/ml) or serum copper/zinc ratio (&gt;1) was the risk factors of NSCLC (OR = 3.10, 11.03, respectively), but the ORs of the higher serum Zn (&gt;1200 ng/ml), Se (&gt;50 ng/ml) or Cr3+ (&gt;600 ng/ml) for NSCLC were all significantly less than 0.20 (all p &lt; 0.01) indicating strong protection against NSCLC. While the OR of CYP 1A1 variants carriers with a higher serum Cu or Cu/Zn ratio level was around 3.38 and 12.59, respectively, the risk of CYP1A1 variants carriers with a higher serum Zn is 0.18, Se 0.04 or Cr3+ 0.28. Similarly, compared with the carriers of GSTM1 power with a lower serum Zn, Se or Cr3+ , the OR of the carriers of GSTM1 null with a higher serum Zn, Se and Cr3+ was separately 0.16, 0.07 and 0.26, highlighting the protection against NSCLC. 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Based on a hospital based case–control study, the epidemiological questionnaires were completed by face to face interview, and the gene polymorphisms were tested by RFLP–PCR, and serum trace metals were measured by atomic absorption spectrophotometer, and the data was analyzed by the logistic regressive models. Results : The high serum copper level (&gt;1500 ng/ml) or serum copper/zinc ratio (&gt;1) was the risk factors of NSCLC (OR = 3.10, 11.03, respectively), but the ORs of the higher serum Zn (&gt;1200 ng/ml), Se (&gt;50 ng/ml) or Cr3+ (&gt;600 ng/ml) for NSCLC were all significantly less than 0.20 (all p &lt; 0.01) indicating strong protection against NSCLC. While the OR of CYP 1A1 variants carriers with a higher serum Cu or Cu/Zn ratio level was around 3.38 and 12.59, respectively, the risk of CYP1A1 variants carriers with a higher serum Zn is 0.18, Se 0.04 or Cr3+ 0.28. Similarly, compared with the carriers of GSTM1 power with a lower serum Zn, Se or Cr3+ , the OR of the carriers of GSTM1 null with a higher serum Zn, Se and Cr3+ was separately 0.16, 0.07 and 0.26, highlighting the protection against NSCLC. Conclusions : Our findings suggested that CYP1A1 or GSTM1 variants may significantly modify the associations between level of serum trace metals (Cu, Zn, Se or Cr) and NSCLC, indicating the intriguing pathogenesis of lung cancer.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>20638923</pmid><doi>10.1016/j.canep.2010.06.004</doi><tpages>6</tpages></addata></record>
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subjects Cancer
Carcinoma, Non-Small-Cell Lung - blood
Carcinoma, Non-Small-Cell Lung - enzymology
Carcinoma, Non-Small-Cell Lung - genetics
Case-Control Studies
China - epidemiology
Combined effect
Cytochrome P-450 CYP1A1 - genetics
Epidemiology
Female
Gene polymorphism
Genetic Predisposition to Disease
Glutathione Transferase - genetics
Hematology, Oncology and Palliative Medicine
Humans
Internal Medicine
Lung cancer
Male
Metals
Middle Aged
Non-small cell lung cancer (NSCLC)
Risk Factors
Serum trace metal
Smoking
Studies
Trace elements
Trace Elements - blood
title Combined effects of serum trace metals and polymorphisms of CYP1A1 or GSTM1 on non-small cell lung cancer: A hospital based case–control study in China
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