<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nan FY</submitter><funding>Zhenjiang Clinical Research Center of Hematology</funding><funding>Medical Innovation Team of Jiangsu Province</funding><funding>Scientific Research Project of The Fifth 169 Project of Zhenjian</funding><funding>National Natural Science Foundation of China</funding><funding>Social Development Foundation of Zhenjiang</funding><pagination>5283-5296</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8335806</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(15)</volume><pubmed_abstract>It was previously reported that PRR34-AS1 was overexpressed in some solid tumors. PRR34-AS1 promoter was shown to have a differential methylation region (DMR), and was hypomethylated in acute myeloid leukemia (AML). Therefore, the present study used real-time quantitative PCR (RQ-PCR) to explore the expression characteristics of PRR34-AS1 in AML. In addition, the correlation between the expression of PRR34-AS1 and clinical prognosis of AML was determined. The findings of this study indicated that high PRR34-AS1 expression was bound up with shorter overall survival (OS) in AML patients (p = 0.002). Moreover, patients with high expression of PRR34-AS1 had significantly lower complete remission (CR) rate compared with those with low expression of PRR34-AS1 after induction chemotherapy. Furthe</pubmed_abstract><journal>Cancer medicine</journal><pubmed_title>Abnormal expression and methylation of PRR34-AS1 are associated with adverse outcomes in acute myeloid leukemia.</pubmed_title><pmcid>PMC8335806</pmcid><funding_grant_id>81900166</funding_grant_id><funding_grant_id>SH2019065</funding_grant_id><funding_grant_id>SH2019067</funding_grant_id><funding_grant_id>SS2018009</funding_grant_id><funding_grant_id>81970118</funding_grant_id><funding_grant_id>81900163</funding_grant_id><funding_grant_id>CXTDB2017002</funding_grant_id><pubmed_authors>Qian J</pubmed_authors><pubmed_authors>Gu Y</pubmed_authors><pubmed_authors>Nan FY</pubmed_authors><pubmed_authors>Lin J</pubmed_authors><pubmed_authors>Zhou JD</pubmed_authors><pubmed_authors>Ma JC</pubmed_authors><pubmed_authors>Sun GK</pubmed_authors><pubmed_authors>Leng JY</pubmed_authors><pubmed_authors>Xu ZJ</pubmed_authors><pubmed_authors>Zhang TJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Abnormal expression and methylation of PRR34-AS1 are associated with adverse outcomes in acute myeloid leukemia.</name><description>It was previously reported that PRR34-AS1 was overexpressed in some solid tumors. PRR34-AS1 promoter was shown to have a differential methylation region (DMR), and was hypomethylated in acute myeloid leukemia (AML). Therefore, the present study used real-time quantitative PCR (RQ-PCR) to explore the expression characteristics of PRR34-AS1 in AML. In addition, the correlation between the expression of PRR34-AS1 and clinical prognosis of AML was determined. The findings of this study indicated that high PRR34-AS1 expression was bound up with shorter overall survival (OS) in AML patients (p = 0.002). Moreover, patients with high expression of PRR34-AS1 had significantly lower complete remission (CR) rate compared with those with low expression of PRR34-AS1 after induction chemotherapy. Furthe</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Aug</publication><modification>2026-05-08T16:57:33.414Z</modification><creation>2022-02-11T06:05:04.27Z</creation></dates><accession>S-EPMC8335806</accession><cross_references><pubmed>34227248</pubmed><doi>10.1002/cam4.4085</doi></cross_references></HashMap>