Expression profile of apoptosis-related genes in childhood adrenocortical tumors: low level of expression of BCL2 and TNF genes suggests a poor prognosis


Autoria(s): Lorea, Cecília Fernandes; Moreno, Daniel Antunes; Borges, Kleiton Silva; Martinelli, Carlos Eduardo, Jr.; Antonini, Sonir Roberto Rauber; Castro, Margaret de; Tucci, Silvio, Jr.; Serafini, Luciano Neder; Ramalho, Leandra Naira Zambelli; Cardinalli, Izilda; Seidinger, Ana Luiza; Mastellaro, Maria Jose; Yunes, José Andrés; Brandalise, Silvia Regina; Tone, Luiz Gonzaga; Scrideli, Carlos Alberto
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

05/11/2013

05/11/2013

2012

Resumo

Background: Impaired apoptosis has been implicated in the development of childhood adrenocortical tumors (ACT), although the expression of apoptosis-related gene expression in such tumors has not been reported. Methods: The mRNA expression levels of the genes CASP3, CASP8, CASP9, FAS, TNF, NFKB, and BCL2 were analyzed by quantitative real-time PCR in consecutive tumor samples obtained at diagnosis from 60 children with a diagnosis of ACT and in 11 non-neoplastic adrenal samples. BCL2 and TNF protein expression was analyzed by immunohistochemistry. Results: A significant association was observed between tumor size >= 100 g and lower expression levels of the BCL2 (P=0.03) and TNF (P=0.05) genes; between stage IV and lower expression levels of CASP3 (P=0.008), CASP9 (P=0.02), BCL2 (P=0.002), TNF (P=0.05), and NFKB (P=0.03); Weiss score >= 3 and lower expression of TNF (P=0.01); unfavorable event and higher expression values of CASP9 (P=0.01) and lower values of TNF (P=0.02); and death and lower expression of BCL2 (P=0.04). Underexpression of TNF was associated with lower event-free survival in uni- and multivariate analyses (P<0.01). Similar results were observed when patients with Weiss score <3 were excluded. Conclusion: This study supports the participation of apoptosis-related genes in the biology and prognosis of childhood ACT and suggests the complex role of these genes in the pathogenesis of this tumor.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

FAEPA (Brazil)

FAEPA (Brazil)

Identificador

EUROPEAN JOURNAL OF ENDOCRINOLOGY, BRISTOL, v. 167, n. 2, pp. 199-208, AUG, 2012

0804-4643

http://www.producao.usp.br/handle/BDPI/41529

10.1530/EJE-12-0183

http://dx.doi.org/10.1530/EJE-12-0183

Idioma(s)

eng

Publicador

BIOSCIENTIFICA LTD

BRISTOL

Relação

EUROPEAN JOURNAL OF ENDOCRINOLOGY

Direitos

restrictedAccess

Copyright BIOSCIENTIFICA LTD

Palavras-Chave #NF-KAPPA-B #CANCER DEVELOPMENT #TREATMENT RESPONSE #ADRENAL-CORTEX #CARCINOMA #CHILDREN #P53 #PROGRESSION #GROWTH #FETAL #ENDOCRINOLOGY & METABOLISM
Tipo

article

original article

publishedVersion