Oral Oncology
Volume 48, Issue 2 , Pages 130-135, February 2012

A high HIF-1α expression genotype is associated with poor prognosis of upper aerodigestive tract carcinoma patients

  • Carlos Alberto de Carvalho Fraga

      Affiliations

    • Department of Dentistry, Universidade Estadual de Montes Claros, Montes Claros, Brazil
  • ,
  • Marcos Vinícius Macedo de Oliveira

      Affiliations

    • Department of Dentistry, Universidade Estadual de Montes Claros, Montes Claros, Brazil
  • ,
  • Érica Silva de Oliveira

      Affiliations

    • Department of Dentistry, Universidade Estadual de Montes Claros, Montes Claros, Brazil
  • ,
  • Lucas Oliveira Barros

      Affiliations

    • Department of Dentistry, Universidade Estadual de Montes Claros, Montes Claros, Brazil
  • ,
  • Francis Balduino Guimarães Santos

      Affiliations

    • Department of Medicine, Universidade Estadual de Montes Claros, Montes Claros, Brazil
  • ,
  • Ricardo Santiago Gomez

      Affiliations

    • Department of Clinical, Surgery and Oral Pathology, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil
  • ,
  • Alfredo Maurício Batista De-Paula

      Affiliations

    • Department of Dentistry, Universidade Estadual de Montes Claros, Montes Claros, Brazil
  • ,
  • André Luiz Sena Guimarães

      Affiliations

    • Department of Dentistry, Universidade Estadual de Montes Claros, Montes Claros, Brazil
    • Corresponding Author InformationCorresponding author. Address: Universidade Estadual de Montes Claros, Hospital Universitário Clemente de Faria, Laboratório de Pesquisa em Saúde, Avenida Cula Mangabeira, 562, Montes Claros, Minas Gerais, cep 39401-001, Brazil.

Received 23 May 2011; received in revised form 16 August 2011; accepted 28 August 2011. published online 26 September 2011.

Summary 

The aim of the present study was to evaluate the role of HIF-1α genetic polymorphisms and protein expression in the development of metastasis in upper aerodigestive tract cancer (UADTC) patients. The expression of pro-angiogenic markers was also evaluated. Protein expression was analysed using immunohistochemistry, and RFLP analysis was used to investigate HIF-1α C1779T and G1790A polymorphisms in 52 patients with UADTC. Primary lesions were divided into 2 groups according to the absence or presence of metastasis. Lymph node samples were divided into 3 groups: metastatic lymph nodes, non-metastatic lymph nodes (both derived from patients with metastatic disease), and control lymph nodes, which were obtained from patients without any metastasis. The allele T was more frequently found in patients with metastatic disease. HIF-1α protein expression in the lymph nodes was increased in the presence of the T allele. Metastatic lymph nodes showed lower levels of HIF-1α, VEGFR1, and MMP-9 proteins compared to lymph nodes without metastasis, while VEGFR2 protein levels were increased. In agreement, HIF-1α expression was correlated with MMP-9. Cox regression analysis demonstrated that higher HIF-1α and MMP-9 protein expression levels and GA and GG genotypes were associated with poor survival. Our findings show that the C1772T and G1790A polymorphisms of the HIF-1α gene are associated with increased expression of the HIF-1α protein in UADTC. The present data indicate that non-metastatic tissues express higher levels of HIF-1α, VEGFR1, and MMP-9, while in metastatic lymph nodes, VEGFR2 protein expression is elevated. The present study also shows that the HIF-1α G1790A polymorphism and its protein expression have an impact on the prognosis of UADTC patients.

Keywords: Metastasis, Angiogenesis, Hypoxia, HIF, Polymorphism, VEGFR1, Upper aerodigestive tract cancer

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S1368-8375(11)00812-8

doi:10.1016/j.oraloncology.2011.08.023

Oral Oncology
Volume 48, Issue 2 , Pages 130-135, February 2012