Expression of CYP1A1 Gene in Patients With Lung Cancer: Evidence for Cigarette Smoke-Induced Gene Expression in Normal Lung Tissue and for Altered Gene Regulation in Primary Pulmonary Carcinomas
The major polycyclic aromatic hydrocarbon inducible-cy-tochrome P4501A1 gene (CYP1A1) is presumed to be important in pulmonary carcinogenesis and toxicology because its product, the cytochrome P4501Al-dependent (CYPlAl-de-pendent) monooxygenase, transforms selected xenobiotics (including polycyclic...
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creator | McLemore, Theodore L. Adelberg, Steven Liu, Mark C. McMahon, Noreen A. Yu, Sha Jin Hubbard, Walter C. Czerwinski, Maciej Wood, Thomas G. Storeng, Ritsa Lubet, Ronald A. Eggleston, Joseph C. Boyd, Michael R. Hines, Ronald N. |
description | The major polycyclic aromatic hydrocarbon inducible-cy-tochrome P4501A1 gene (CYP1A1) is presumed to be important in pulmonary carcinogenesis and toxicology because its product, the cytochrome P4501Al-dependent (CYPlAl-de-pendent) monooxygenase, transforms selected xenobiotics (including polycyclic aromatic hydrocarbon procarcinogens in cigarette smoke) to potent carcinogenic metabolites. CYPIAI messenger RNA (mRNA) expression has not, however, been previously demonstrated in human pulmonary tissue. This report defines CYP1A1 gene expression in normal lung tissue and primary pulmonary carcinoma tissue obtained at thoracotomy from 56 patients with lung cancer. When Northern blot hybridization analyses were performed, 17 of 19 (89%) and zero of five (0%) samples of normal lung tissue from active cigarette smokers and nonsmokers, respectively, expressed the normal 2.8-kilobase CYPIAI mRNA. In addition, a time-dependent decrease in expression of the CYPIAI gene was noted in normal lung tissue from individuals who were former smokers, with a decrease in expression occurring as early as 2 weeks following cessation of cigarette smoking. Expression became undetectable in all patients who had stopped smoking more than 6 weeks prior to study. When CYPIAI gene expression was evaluated in lung cancers, mRNA levels were detectable in one of four (25%) tumors from nonsmokers; two of 24 (8%) tumors from former smokers; and seven of 15 (47%) tumors from cigarette smokers. In addition, an approximately 10-kilobase CYPIAI RNA species, which was not detectable in normal lung tissue, was observed in five of ten (50%) of the lung cancers that expressed the CYPIAI gene. There was no positive association between CYPIAI expression and lung cancer histologic cell type nor between CYPIAI mRNA levels in matched normal lung tissue and tumor tissue from patients with lung cancer. These results demonstrate a positive association between active cigarette smoking and CYPIAI gene expression in normal human lung tissue. Moreover, CYPIAI gene expression was documented in many pulmonary carcinomas, and altered regulation of the gene was also observed in several lung tumors. [J Natl Cancer Inst 82: 1333–1339, 1990] |
doi_str_mv | 10.1093/jnci/82.16.1333 |
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CYPIAI messenger RNA (mRNA) expression has not, however, been previously demonstrated in human pulmonary tissue. This report defines CYP1A1 gene expression in normal lung tissue and primary pulmonary carcinoma tissue obtained at thoracotomy from 56 patients with lung cancer. When Northern blot hybridization analyses were performed, 17 of 19 (89%) and zero of five (0%) samples of normal lung tissue from active cigarette smokers and nonsmokers, respectively, expressed the normal 2.8-kilobase CYPIAI mRNA. In addition, a time-dependent decrease in expression of the CYPIAI gene was noted in normal lung tissue from individuals who were former smokers, with a decrease in expression occurring as early as 2 weeks following cessation of cigarette smoking. Expression became undetectable in all patients who had stopped smoking more than 6 weeks prior to study. When CYPIAI gene expression was evaluated in lung cancers, mRNA levels were detectable in one of four (25%) tumors from nonsmokers; two of 24 (8%) tumors from former smokers; and seven of 15 (47%) tumors from cigarette smokers. In addition, an approximately 10-kilobase CYPIAI RNA species, which was not detectable in normal lung tissue, was observed in five of ten (50%) of the lung cancers that expressed the CYPIAI gene. There was no positive association between CYPIAI expression and lung cancer histologic cell type nor between CYPIAI mRNA levels in matched normal lung tissue and tumor tissue from patients with lung cancer. These results demonstrate a positive association between active cigarette smoking and CYPIAI gene expression in normal human lung tissue. Moreover, CYPIAI gene expression was documented in many pulmonary carcinomas, and altered regulation of the gene was also observed in several lung tumors. [J Natl Cancer Inst 82: 1333–1339, 1990]</description><identifier>ISSN: 0027-8874</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/82.16.1333</identifier><identifier>PMID: 2380990</identifier><language>eng</language><publisher>Cary, NC: Oxford University Press</publisher><subject>Biological and medical sciences ; cigarettes ; Cytochrome P-450 CYP1A1 ; Cytochrome P-450 Enzyme System - biosynthesis ; Cytochrome P-450 Enzyme System - genetics ; Cytochrome P-450 Enzyme System - metabolism ; cytochrome P4501A1 ; Female ; Gene Expression Regulation, Neoplastic ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Isoenzymes - biosynthesis ; Isoenzymes - genetics ; Lung - metabolism ; Lung Neoplasms - genetics ; Lung Neoplasms - metabolism ; Male ; Medical sciences ; Middle Aged ; Oxidoreductases - metabolism ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; RNA, Messenger - analysis ; RNA, Neoplasm - analysis ; smoking ; Smoking - adverse effects</subject><ispartof>JNCI : Journal of the National Cancer Institute, 1990-08, Vol.82 (16), p.1333-1339</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-ada0a61d36ab23dc6f9b7aeac1150fb0e37ef154ccf31bbc13542bfbf933c553</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4615293$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2380990$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McLemore, Theodore L.</creatorcontrib><creatorcontrib>Adelberg, Steven</creatorcontrib><creatorcontrib>Liu, Mark C.</creatorcontrib><creatorcontrib>McMahon, Noreen A.</creatorcontrib><creatorcontrib>Yu, Sha Jin</creatorcontrib><creatorcontrib>Hubbard, Walter C.</creatorcontrib><creatorcontrib>Czerwinski, Maciej</creatorcontrib><creatorcontrib>Wood, Thomas G.</creatorcontrib><creatorcontrib>Storeng, Ritsa</creatorcontrib><creatorcontrib>Lubet, Ronald A.</creatorcontrib><creatorcontrib>Eggleston, Joseph C.</creatorcontrib><creatorcontrib>Boyd, Michael R.</creatorcontrib><creatorcontrib>Hines, Ronald N.</creatorcontrib><title>Expression of CYP1A1 Gene in Patients With Lung Cancer: Evidence for Cigarette Smoke-Induced Gene Expression in Normal Lung Tissue and for Altered Gene Regulation in Primary Pulmonary Carcinomas</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>J Natl Cancer Inst</addtitle><description>The major polycyclic aromatic hydrocarbon inducible-cy-tochrome P4501A1 gene (CYP1A1) is presumed to be important in pulmonary carcinogenesis and toxicology because its product, the cytochrome P4501Al-dependent (CYPlAl-de-pendent) monooxygenase, transforms selected xenobiotics (including polycyclic aromatic hydrocarbon procarcinogens in cigarette smoke) to potent carcinogenic metabolites. CYPIAI messenger RNA (mRNA) expression has not, however, been previously demonstrated in human pulmonary tissue. This report defines CYP1A1 gene expression in normal lung tissue and primary pulmonary carcinoma tissue obtained at thoracotomy from 56 patients with lung cancer. When Northern blot hybridization analyses were performed, 17 of 19 (89%) and zero of five (0%) samples of normal lung tissue from active cigarette smokers and nonsmokers, respectively, expressed the normal 2.8-kilobase CYPIAI mRNA. In addition, a time-dependent decrease in expression of the CYPIAI gene was noted in normal lung tissue from individuals who were former smokers, with a decrease in expression occurring as early as 2 weeks following cessation of cigarette smoking. Expression became undetectable in all patients who had stopped smoking more than 6 weeks prior to study. When CYPIAI gene expression was evaluated in lung cancers, mRNA levels were detectable in one of four (25%) tumors from nonsmokers; two of 24 (8%) tumors from former smokers; and seven of 15 (47%) tumors from cigarette smokers. In addition, an approximately 10-kilobase CYPIAI RNA species, which was not detectable in normal lung tissue, was observed in five of ten (50%) of the lung cancers that expressed the CYPIAI gene. There was no positive association between CYPIAI expression and lung cancer histologic cell type nor between CYPIAI mRNA levels in matched normal lung tissue and tumor tissue from patients with lung cancer. These results demonstrate a positive association between active cigarette smoking and CYPIAI gene expression in normal human lung tissue. Moreover, CYPIAI gene expression was documented in many pulmonary carcinomas, and altered regulation of the gene was also observed in several lung tumors. [J Natl Cancer Inst 82: 1333–1339, 1990]</description><subject>Biological and medical sciences</subject><subject>cigarettes</subject><subject>Cytochrome P-450 CYP1A1</subject><subject>Cytochrome P-450 Enzyme System - biosynthesis</subject><subject>Cytochrome P-450 Enzyme System - genetics</subject><subject>Cytochrome P-450 Enzyme System - metabolism</subject><subject>cytochrome P4501A1</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Isoenzymes - biosynthesis</subject><subject>Isoenzymes - genetics</subject><subject>Lung - metabolism</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Oxidoreductases - metabolism</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Neoplasm - analysis</subject><subject>smoking</subject><subject>Smoking - adverse effects</subject><issn>0027-8874</issn><issn>1460-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkUGP0zAQhS0EWsrCmROSD4hbWjuO44RbNyrblQpUbEWBi-U44-LdxCl2gpa_xy8jIaXCF4_03vtmpIfQS0rmlORscee0XWTxnKZzyhh7hGY0SUkUU8IfoxkhsYiyTCRP0bMQ7sjw8ji5QBcxy0iekxn6vXo4egjBtg63Bhdft3RJ8TU4wNbhreosuC7gve2-403vDrhQToN_i1c_bQXDiE3rcWEPykPXAb5t2nuIblzVa6gmzn8bBuSH1jeqnlg7G0IPWLnqL2VZd-D_pT7Boa-H9VNq622j_C-87eumdeNUKK-taxsVnqMnRtUBXpz-S7R7t9oV62jz8fqmWG4izXLSRapSRKW0YqkqY1bp1OSlUKA0pZyYkgATYChPtDaMlqWmjCdxaUqTM6Y5Z5fozYQ9-vZHD6GTjQ0a6lo5aPsgKRckEVwMxsVk1L4NwYORx-l6SYkcS5NjaTKLJU3lWNqQeHVC92UD1dl_amnQX590FbSqjR86sOFsS1LK43zERJPNhg4ezrLy9zIVTHC5_vJNiv3V-vP-lsj37A-TAbJ-</recordid><startdate>19900815</startdate><enddate>19900815</enddate><creator>McLemore, Theodore L.</creator><creator>Adelberg, Steven</creator><creator>Liu, Mark C.</creator><creator>McMahon, Noreen A.</creator><creator>Yu, Sha Jin</creator><creator>Hubbard, Walter C.</creator><creator>Czerwinski, Maciej</creator><creator>Wood, Thomas G.</creator><creator>Storeng, Ritsa</creator><creator>Lubet, Ronald A.</creator><creator>Eggleston, Joseph C.</creator><creator>Boyd, Michael R.</creator><creator>Hines, Ronald N.</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</scope><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>7T3</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>19900815</creationdate><title>Expression of CYP1A1 Gene in Patients With Lung Cancer: Evidence for Cigarette Smoke-Induced Gene Expression in Normal Lung Tissue and for Altered Gene Regulation in Primary Pulmonary Carcinomas</title><author>McLemore, Theodore L. ; Adelberg, Steven ; Liu, Mark C. ; McMahon, Noreen A. ; Yu, Sha Jin ; Hubbard, Walter C. ; Czerwinski, Maciej ; Wood, Thomas G. ; Storeng, Ritsa ; Lubet, Ronald A. ; Eggleston, Joseph C. ; Boyd, Michael R. ; Hines, Ronald N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-ada0a61d36ab23dc6f9b7aeac1150fb0e37ef154ccf31bbc13542bfbf933c553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Biological and medical sciences</topic><topic>cigarettes</topic><topic>Cytochrome P-450 CYP1A1</topic><topic>Cytochrome P-450 Enzyme System - biosynthesis</topic><topic>Cytochrome P-450 Enzyme System - genetics</topic><topic>Cytochrome P-450 Enzyme System - metabolism</topic><topic>cytochrome P4501A1</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Isoenzymes - biosynthesis</topic><topic>Isoenzymes - genetics</topic><topic>Lung - metabolism</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Oxidoreductases - metabolism</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. 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CYPIAI messenger RNA (mRNA) expression has not, however, been previously demonstrated in human pulmonary tissue. This report defines CYP1A1 gene expression in normal lung tissue and primary pulmonary carcinoma tissue obtained at thoracotomy from 56 patients with lung cancer. When Northern blot hybridization analyses were performed, 17 of 19 (89%) and zero of five (0%) samples of normal lung tissue from active cigarette smokers and nonsmokers, respectively, expressed the normal 2.8-kilobase CYPIAI mRNA. In addition, a time-dependent decrease in expression of the CYPIAI gene was noted in normal lung tissue from individuals who were former smokers, with a decrease in expression occurring as early as 2 weeks following cessation of cigarette smoking. Expression became undetectable in all patients who had stopped smoking more than 6 weeks prior to study. When CYPIAI gene expression was evaluated in lung cancers, mRNA levels were detectable in one of four (25%) tumors from nonsmokers; two of 24 (8%) tumors from former smokers; and seven of 15 (47%) tumors from cigarette smokers. In addition, an approximately 10-kilobase CYPIAI RNA species, which was not detectable in normal lung tissue, was observed in five of ten (50%) of the lung cancers that expressed the CYPIAI gene. There was no positive association between CYPIAI expression and lung cancer histologic cell type nor between CYPIAI mRNA levels in matched normal lung tissue and tumor tissue from patients with lung cancer. These results demonstrate a positive association between active cigarette smoking and CYPIAI gene expression in normal human lung tissue. Moreover, CYPIAI gene expression was documented in many pulmonary carcinomas, and altered regulation of the gene was also observed in several lung tumors. [J Natl Cancer Inst 82: 1333–1339, 1990]</abstract><cop>Cary, NC</cop><pub>Oxford University Press</pub><pmid>2380990</pmid><doi>10.1093/jnci/82.16.1333</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences cigarettes Cytochrome P-450 CYP1A1 Cytochrome P-450 Enzyme System - biosynthesis Cytochrome P-450 Enzyme System - genetics Cytochrome P-450 Enzyme System - metabolism cytochrome P4501A1 Female Gene Expression Regulation, Neoplastic Humans Investigative techniques, diagnostic techniques (general aspects) Isoenzymes - biosynthesis Isoenzymes - genetics Lung - metabolism Lung Neoplasms - genetics Lung Neoplasms - metabolism Male Medical sciences Middle Aged Oxidoreductases - metabolism Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques RNA, Messenger - analysis RNA, Neoplasm - analysis smoking Smoking - adverse effects |
title | Expression of CYP1A1 Gene in Patients With Lung Cancer: Evidence for Cigarette Smoke-Induced Gene Expression in Normal Lung Tissue and for Altered Gene Regulation in Primary Pulmonary Carcinomas |
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