ARE HLA DQB1 ALLELES CORRELATED WITH BREAST CANCER HISTOPRONOSTIC PARAMETERS IN TUNISIA?

Authors

  • Amal Baccar Laboratoire de Génétique Immunologie et Pathologies Humaines. Faculté des sciences de Tunis
  • Besma Yacoubi Loueslati Laboratoire de Génétique Immunologie et Pathologies Humaines. Faculté des sciences de Tunis
  • Wafa Troudi Laboratoire de Génétique Immunologie et Pathologies Humaines. Faculté des sciences de Tunis.
  • Slama Hmida Service d'hémato-immunologie du centre national de transfusion sanguine de Tunis
  • Amel Dridi Service d'hémato-immunologie du centre national de transfusion sanguine de Tunis
  • Afef Jridi Service d'hémato-immunologie du centre national de transfusion sanguine de Tunis
  • Karima Mrad Institut de Carcinologie Salah AZAIZ
  • Khaled Ben Romdhane Institut de Carcinologie Salah AZAIZ
  • Amel Ben Ammar Elgaaied Laboratoire de Génétique Immunologie et Pathologies Humaines. Faculté des sciences de Tunis

Keywords:

DQB1, breast cancer, histoprognostical parameters

Abstract

Background: Tumor cells express surface structures different from normal cells. These structures may be recognized by the immune system, which ensure anti-tumoral surveillance. Antigenic presentation requires HLA molecules role. Since, these molecules are encoded by a high polymorphic system, immune response can be modulated according to HLA genotype. So, HLA polymorphism could be correlated with tumor escape from anti-tumor immunosurveillance.
Aim : We have aimed to search for possible associations between HLA DQB1 alleles and the histoprognostical parameters in breast cancer in the Tunisian population.
Methods: DQB1 alleles were determined by PCR-SSO molecular typing in 100 healthy matched and unrelated Tunisian female and 87 Tunisian women with breast cancer.
Results: Allelic distribution between the two studied groups showed no significant associations between this locus and the occurrence, the EE grade and the lymph node invasion of breast cancer in the Tunisian population.
Conclusion: This result may be explained by the fact that cancer is a multifactoral disease due to several interacting factors that might change from one population to another.

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References

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