<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(5)</volume><submitter>Wang L</submitter><pubmed_abstract>Throughout the world, numerous individuals are infected with &lt;i>Toxoplasma gondii&lt;/i>, which may improve immunity against cancer. Furthermore, microRNAs (miRs) may be differentially expressed in the host upon infection with &lt;i>T. gondii&lt;/i>. In the present study, RNA-sequencing analysis and reverse transcription-quantitative PCR revealed that miR-429-3p, miR-145a-5p, miR-211-5p, miR-31-3p and miR-135a-5p were determined to be downregulated, while miR-21a-3p, miR-135b-5p, miR-210-5p and miR-146-3p were upregulated in mice post-infection with &lt;i>T. gondii&lt;/i>. Antitumor genes [TNF receptor superfamily member 11b, large tumor suppressor kinase (Lats)2 and Lats1] were identified as targets of miR-429-3p, miR-145a-5p, miR-211-5p, miR-31-3p and miR-135a-5p with a luciferase reporter assay. In ad</pubmed_abstract><journal>Oncology letters</journal><pagination>149</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8941548</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&lt;i>Toxoplasma gondii&lt;/i> causes changes in the host's expression of cancer-associated miRNAs.</pubmed_title><pmcid>PMC8941548</pmcid><pubmed_authors>Wang N</pubmed_authors><pubmed_authors>Zhao YH</pubmed_authors><pubmed_authors>Lu G</pubmed_authors><pubmed_authors>Wang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;i>Toxoplasma gondii&lt;/i> causes changes in the host's expression of cancer-associated miRNAs.</name><description>Throughout the world, numerous individuals are infected with &lt;i>Toxoplasma gondii&lt;/i>, which may improve immunity against cancer. Furthermore, microRNAs (miRs) may be differentially expressed in the host upon infection with &lt;i>T. gondii&lt;/i>. In the present study, RNA-sequencing analysis and reverse transcription-quantitative PCR revealed that miR-429-3p, miR-145a-5p, miR-211-5p, miR-31-3p and miR-135a-5p were determined to be downregulated, while miR-21a-3p, miR-135b-5p, miR-210-5p and miR-146-3p were upregulated in mice post-infection with &lt;i>T. gondii&lt;/i>. Antitumor genes [TNF receptor superfamily member 11b, large tumor suppressor kinase (Lats)2 and Lats1] were identified as targets of miR-429-3p, miR-145a-5p, miR-211-5p, miR-31-3p and miR-135a-5p with a luciferase reporter assay. In ad</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-04-22T18:19:22.625Z</modification><creation>2025-04-06T02:23:11.541Z</creation></dates><accession>S-EPMC8941548</accession><cross_references><pubmed>35350589</pubmed><doi>10.3892/ol.2022.13267</doi></cross_references></HashMap>