Early Changes in Gene Expression Induced by Tobacco Smoke: Evidence for the Importance of Estrogen within Lung Tissue


Autoria(s): MEIRELES, Sibele I.; ESTEVES, Gustavo H.; HIRATA JR., Roberto; PERI, Suraj; DEVARAJAN, Karthik; SLIFKER, Michael; MOSIER, Stacy L.; PENG, Jing; VADHANAM, Manicka V.; HURST, Harrell E.; NEVES, E. Jordao; REIS, Luiz F.; GAIROLA, C. Gary; GUPTA, Ramesh C.; CLAPPER, Margie L.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Lung cancer is the leading cause of cancer deaths in the United States, surpassing breast cancer as the primary cause of cancer-related mortality in women. The goal of the present study was to identify early molecular changes in the lung induced by exposure to tobacco smoke and thus identify potential targets for chemoprevention. Female A/J mice were exposed to either tobacco smoke or HEPA-filtered air via a whole-body exposure chamber (6 h/d, 5 d/wk for 3, 8, and 20 weeks). Gene expression profiles of lung tissue from control and smoke-exposed animals were established using a 15K cDNA microarray. Cytochrome P450 1b1, a phase I enzyme involved in both the metabolism of xenobiotics and the 4-hydroxylation of 17 beta-estradiol (E(2)), was modulated to the greatest extent following smoke exposure. A panel of 10 genes were found to be differentially expressed in control and smoke-exposed lung tissues at 3, 8, and 20 weeks (P < 0.001). The interaction network of these differentially expressed genes revealed new pathways modulated by short-term smoke exposure, including estrogen metabolism. In addition, E(2) was detected within murine lung tissue by gas chromatography-coupled mass spectrometry and immunohistochemistry. Identification of the early molecular events that contribute to lung tumor formation is anticipated to lead to the development of promising targeted chemopreventive therapies. In conclusion, the presence of E2 within lung tissue when combined with the modulation of cytochrome P450 1b1 and other estrogen metabolism genes by tobacco smoke provides novel insight into a possible role for estrogens in lung cancer. Cancer Prev Res; 3(6); 707-17. (C) 2010 AACR.

National Cancer Institute (NCI/NIH)[CA-06927]

National Cancer Institute (NCI/NIH)

National Cancer Institute[CA-96310]

National Cancer Institute

National Cancer Institute (NCI/NIH)

National Cancer Institute (NCI/NIH)[CA-118114]

National Cancer Institute (NCI/NIH)[CA-125152]

National Cancer Institute (NCI/NIH)

Commonwealth of Pennsylvania

Commonwealth of Pennsylvania

PA Department of Health

PA Department of Health

Jerome M. Spencer and Arnold Zaslow Family Foundation

Jerome M. Spencer and Arnold Zaslow Family Foundation

University of Kentucky and University of Louisville

University of Kentucky and University of Louisville

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP Funda ao de Amparo a Pesquisa do Estado de Sao Paulo [Brazil][98/14335-2]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP Funda ao de Amparo a Pesquisa do Estado de Sao Paulo [99/11962-9]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP Funda ao de Amparo a Pesquisa do Estado de Sao Paulo [99/07390-0]

Identificador

CANCER PREVENTION RESEARCH, v.3, n.6, p.707-717, 2010

1940-6207

http://producao.usp.br/handle/BDPI/30371

10.1158/1940-6207.CAPR-09-0162

http://dx.doi.org/10.1158/1940-6207.CAPR-09-0162

Idioma(s)

eng

Publicador

AMER ASSOC CANCER RESEARCH

Relação

Cancer Prevention Research

Direitos

restrictedAccess

Copyright AMER ASSOC CANCER RESEARCH

Palavras-Chave #MAINSTREAM CIGARETTE-SMOKE #HISTIDINE-DECARBOXYLASE #CATECHOL ESTROGENS #CANCER #WOMEN #MOUSE #CARCINOGENICITY #SUSCEPTIBILITY #CARCINOMA #TUMORS #Oncology
Tipo

article

original article

publishedVersion