<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>56(3)</volume><submitter>Zubair H</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>AKT, also called protein kinase B, is a serine-threonine kinase that functions as a mediator of PI3K-Akt-mTOR signaling pathway and plays an important role in an array of cellular processes. Many single nucleotide polymorphisms (SNP) in &lt;i>AKT&lt;/i> gene have been observed to be associated with various types of cancers. In the current research the association of a functional SNP rs1130233 in &lt;i>AKT&lt;/i>, depicting G to A transition, was studied with AKT activation, DNA damage, an early response B-cell translocation gene 2 (Btg2) expression and risk of colorectal cancer (CRC) development.&lt;h4>Patients and methods&lt;/h4>A total 197 population-based controls and 200 CRC patients were genotyped for SNP rs1130233. AKT expression, activation and &lt;i>BTG2&lt;/i> expression were determine</pubmed_abstract><journal>Radiology and oncology</journal><pagination>336-345</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9400445</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Impact of &lt;i>AKT1&lt;/i> polymorphism on DNA damage, &lt;i>BTG2&lt;/i> expression, and risk of colorectal cancer development.</pubmed_title><pmcid>PMC9400445</pmcid><pubmed_authors>Imran M</pubmed_authors><pubmed_authors>Khan Z</pubmed_authors><pubmed_authors>Zubair H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of &lt;i>AKT1&lt;/i> polymorphism on DNA damage, &lt;i>BTG2&lt;/i> expression, and risk of colorectal cancer development.</name><description>&lt;h4>Background&lt;/h4>AKT, also called protein kinase B, is a serine-threonine kinase that functions as a mediator of PI3K-Akt-mTOR signaling pathway and plays an important role in an array of cellular processes. Many single nucleotide polymorphisms (SNP) in &lt;i>AKT&lt;/i> gene have been observed to be associated with various types of cancers. In the current research the association of a functional SNP rs1130233 in &lt;i>AKT&lt;/i>, depicting G to A transition, was studied with AKT activation, DNA damage, an early response B-cell translocation gene 2 (Btg2) expression and risk of colorectal cancer (CRC) development.&lt;h4>Patients and methods&lt;/h4>A total 197 population-based controls and 200 CRC patients were genotyped for SNP rs1130233. AKT expression, activation and &lt;i>BTG2&lt;/i> expression were determine</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-25T23:37:18.298Z</modification><creation>2024-11-06T18:45:58.304Z</creation></dates><accession>S-EPMC9400445</accession><cross_references><pubmed>35962953</pubmed><doi>10.2478/raon-2022-0031</doi></cross_references></HashMap>