The p53 mutationdeletion profile in a small cohort of the omani population with diffuse large B-cell lymphoma

Abstract EN

Objectives: Mutations/deletions affecting the TP53 gene are considered an independent marker predicting a poor prognosis for patients with diffuse large B-cell lymphoma (DLBCL).

A cohort within a genetically isolated population was investigated for p53 mutation/deletion status.

Methods: Deoxyribonucleic acid (DNA) samples were extracted from 23 paraffin-embedded blocks obtained from DLBCL patients, and subjected to polymerase chain reaction (PCR) amplification and sequencing of exons 4–9 of the p53 gene.

Results: While 35% of patients analysed displayed allelic deletions (P <0.01), immunohistochemical analysis revealed a mutation rate of 69.5%.

It is noteworthy that the rate of p53 mutations/deletions in this small cohort was found to be higher than that previously reported in the literature.

Interestingly, patients with p53 mutations displayed a better overall survival when compared to those without.

The survival of patients treated with rituximab-containing combination chemotherapy was significantly better than those who did not receive rituximab (P <0.05).

Furthermore, a modelling analysis of the deleted form of p53 revealed a huge structural change affecting the DNA-binding domain.

Conclusion: The TP53 mutation/deletion status plays a role in mechanism(s) ruling the pathogenesis of DLBCL and may be useful for stratifying patients into distinct prognostic subsets.