Analysis of Cancer-associated Mutations of POLB using Machine Learning and Bioinformatics

Razan Alkhanbouli, Amira Al-Aamri, Maher Maalouf, Kamal Taha, Andreas Henschel, Dirar Homouz

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

DNA damage is a critical factor in the onset and progression of cancer. When DNA is damaged, the number of genetic mutations increases, making it necessary to activate DNA repair mechanisms. A crucial factor in the base excision repair process, which helps maintain the stability of the genome, is an enzyme called DNA polymerase <inline-formula><tex-math notation="LaTeX">$\boldsymbol{\upbeta}$</tex-math></inline-formula> (Pol<inline-formula><tex-math notation="LaTeX">$\boldsymbol{\upbeta}$</tex-math></inline-formula>) encoded by the POLB gene. It plays a vital role in the repair of damaged DNA. Additionally, variations known as Single Nucleotide Polymorphisms (SNPs) in the POLB gene can potentially affect the ability to repair DNA. This study uses bioinformatics tools that extract important features from SNPs to construct a feature matrix, which is then used in combination with machine learning algorithms to predict the likelihood of developing cancer associated with a specific mutation. Eight different machine learning algorithms were used to investigate the relationship between POLB gene variations and their potential role in cancer onset. This study not only highlights the complex link between POLB gene SNPs and cancer, but also underscores the effectiveness of machine learning approaches in genomic studies, paving the way for advanced predictive models in genetic and cancer research.

Original languageBritish English
Pages (from-to)1-10
Number of pages10
JournalIEEE/ACM Transactions on Computational Biology and Bioinformatics
DOIs
StateAccepted/In press - 2024

Keywords

  • Bioinformatics
  • DNA Damage Repair
  • Machine Learning
  • POLB
  • SNPs

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