Frequent downregulation of the transcription factor Foxa2 in lung cancer through epigenetic silencing


Autoria(s): Bassères, Daniela Sanchez; D'Alò, Francesco; Yeap, Beow Y.; Loewenberg, Ester C.; Gonzalez, David A.; Yasuda, Hiroyuki; Dayaram, Tajhal; Kocher, Olivier N.; Godleski, John J.; Richards, William G.; Meyerson, Matthew; Kobayashi, Susumu; Tenen, Daniel G.; Halmos, Balázs; Silva, Bruno Daniel da Costa e
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

25/10/2013

25/10/2013

2012

Resumo

Purpose: We sought to determine the mechanisms of downregulation of the airway transcription factor Foxa2 in lung cancer and the expression status of Foxa2 in non-small-cell lung cancer (NSCLC). Methods: A series of 25 lung cancer cell lines were evaluated for Foxa2 protein expression, FOXA2 mRNA levels, FOXA2 mutations, FOXA2 copy number changes and for evidence of FOXA2 promoter hypermethylation. In addition, 32 NSCLCs were sequenced for FOXA2 mutations and 173 primary NSCLC tumors evaluated for Foxa2 expression using an immunohistochemical assay. Results: Out of the 25 cell lines, 13 (52%) had undetectable FOXA2 mRNA. The expression of FOXA2 mRNA and Foxa2 protein were congruent in 19/22 cells (p = 0.001). FOXA2 mutations were not identified in primary NSCLCs and were infrequent in cell lines. Focal or broad chromosomal deletions involving FOXA2 were not present. The promoter region of FOXA2 had evidence of hypermethylation, with an inverse correlation between FOXA2 mRNA expression and presence of CpG dinucleotide methylation (p < 0.0001). In primary NSCLC tumor specimens, there was a high frequency of either absence (42/173, 24.2%) or no/low expression (96/173,55.4%) of Foxa2. In 130 patients with stage I NSCLC there was a trend towards decreased survival in tumors with no/low expression of Foxa2 (HR of 1.6, 95%CI 0.9-3.1; p = 0.122). Conclusions: Loss of expression of Foxa2 is frequent in lung cancer cell lines and NSCLCs. The main mechanism of downregulation of Foxa2 is epigenetic silencing through promoter hypermethylation. Further elucidation of the involvement of Foxa2 and other airway transcription factors in the pathogenesis of lung cancer may identify novel therapeutic targets. (C) 2012 Elsevier Ireland Ltd. All rights reserved.

Pfizer

Pfizer

Roche

Roche

AstraZeneca

AstraZeneca

American Society of Clinical Oncology Conquer Cancer Foundation

American Society of Clinical Oncology Conquer Cancer Foundation

American Association for Cancer Research

American Association for Cancer Research

Clinical Investigator Training Program at Beth Israel Deaconess Medical Center

Clinical Investigator Training Program at Beth Israel Deaconess Medical Center

American Cancer Society [RSG 11-186]

American Cancer Society

FAMRI Young Clinical Scientist award

FAMRI Young Clinical Scientist award

National Institutes of Health

National Institutes of Health [CA090578]

Identificador

LUNG CANCER, CLARE, v. 77, n. 1, p. 31-37, JUL, 2012

0169-5002

http://www.producao.usp.br/handle/BDPI/36095

10.1016/j.lungcan.2012.01.011

http://dx.doi.org/10.1016/j.lungcan.2012.01.011

Idioma(s)

eng

Publicador

ELSEVIER IRELAND LTD

CLARE

Relação

Lung Cancer

Direitos

closedAccess

Copyright ELSEVIER IRELAND LTD

Palavras-Chave #LUNG CANCER #NON-SMALL-CELL LUNG CANCER #FOXA2 #METHYLATION #TRANSCRIPTION FACTORS #EPIGENETIC #DOWNREGULATION #ADENOCARCINOMA #MUTATION #PROGNOSIS #HEPATOCYTE NUCLEAR FACTOR-3 #C/EBP-ALPHA #GENE AMPLIFICATION #PROTEIN EXPRESSION #TUMOR-SUPPRESSOR #ADENOCARCINOMA #SOX2 #MORPHOGENESIS #TRANSITION #ONCOGENE #ONCOLOGY #RESPIRATORY SYSTEM
Tipo

article

original article

publishedVersion