AI Article Synopsis

  • Lysosomal protein transmembrane 4β (TMEM4β) is identified as an oncogene that is overexpressed in various cancers, with a study investigating its polymorphisms related to diffuse large B-cell lymphoma (DLBCL) and patient prognosis.
  • The study analyzed genetic data from 164 DLBCL patients and 350 healthy individuals using polymerase chain reaction and logistic regression, revealing no significant differences in allele frequencies that would suggest TMEM4β increases DLBCL risk.
  • Although no strong associations were found between TMEM4β polymorphisms and overall survival or disease-free survival, patients with specific genotypes and higher International Prognostic Index scores showed a tendency for better prognostic outcomes.

Article Abstract

Lysosomal protein transmembrane 4β () is an oncogene that is overexpressed in a number of various types of human cancer. There are two known alleles of : and . The present study assessed the association between polymorphisms and the susceptibility to diffuse large B-cell lymphoma (DLBCL) and its prognosis. genotypes were determined using polymerase chain reaction analysis in 164 DLBCL and 350 healthy control cases. The association between polymorphisms and the risk of DLBCL was analyzed using unconditional logistic regression. Differences in patient survival were calculated using Kaplan-Meier analysis. The present study indicated no significant differences (P>0.05) in the frequency of alleles between DLBCL cases (26.5%) and controls (24.1%). The risk of DLBCL was slightly increased in cases with the genotype [odds ratio (OR)=1.160; 95% confidence interval (CI)=0.781-1.724] or the genotype (OR=1.446; 95% CI=0.648-3.227) compared with those with the genotype. There was no significant association between the presence of the allele and overall survival (OS) and disease-free survival (DFS) in patients with DLBCL (P=0.399 and 0.520, respectively). However, there was a tendency for patients with and International Prognostic Index (IPI) score 3-5 to have longer OS and DFS (P=0.126 and 0.109, respectively). These findings suggest that genetic polymorphisms of is not a risk factor for the development of DLBCL, but the allele may a better prognostic indicator in patients with IPI score 3-5 in DLBCL.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768069PMC
http://dx.doi.org/10.3892/ol.2017.7318DOI Listing

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