Molecular Profile of Important Genes for Radiogenomics in the Amazon Indigenous Population.
Milena Cardoso de LimaCinthia Costa de CastroKaio Evandro Cardoso AguiarNatasha MonteGiovanna Gilioli da Costa NunesAna Caroline Alves da CostaJuliana Carla Gomes RodriguesJoão Farias GuerreiroÂndrea Kely Campos Ribeiro Dos SantosPaulo Pimentel de AssumpçãoRommel Mario Rodríguez BurbanoMarianne Rodrigues FernandesSidney Emanuel Batista Dos SantosNey Pereira Carneiro Dos SantosPublished in: Journal of personalized medicine (2024)
Radiotherapy is focused on the tumor but also reaches healthy tissues, causing toxicities that are possibly related to genomic factors. In this context, radiogenomics can help reduce the toxicity, increase the effectiveness of radiotherapy, and personalize treatment. It is important to consider the genomic profiles of populations not yet studied in radiogenomics, such as the indigenous Amazonian population. Thus, our objective was to analyze important genes for radiogenomics, such as ATM , TGFB1 , RAD51 , AREG , XRCC4 , CDK1, MEG3 , PRKCE , TANC1 , and KDR , in indigenous people and draw a radiogenomic profile of this population. The NextSeq 500 ® platform was used for sequencing reactions; for differences in the allelic frequency between populations, Fisher's Exact Test was used. We identified 39 variants, 2 of which were high impact: 1 in KDR (rs41452948) and another in XRCC4 (rs1805377). We found four modifying variants not yet described in the literature in PRKCE . We did not find any variants in TANC1 -an important gene for personalized medicine in radiotherapy-that were associated with toxicities in previous cohorts, configuring a protective factor for indigenous people. We identified four SNVs (rs664143, rs1801516, rs1870377, rs1800470) that were associated with toxicity in previous studies. Knowing the radiogenomic profile of indigenous people can help personalize their radiotherapy.
Keyphrases
- copy number
- early stage
- dna repair
- locally advanced
- genome wide
- radiation therapy
- radiation induced
- systematic review
- dna damage
- gene expression
- oxidative stress
- randomized controlled trial
- genome wide identification
- dna methylation
- single cell
- cell proliferation
- transcription factor
- smoking cessation
- genome wide analysis
- genetic diversity