<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(6)</volume><submitter>Narimani M</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Acute myelocytic leukemia (AML) is a clonal malignancy resulting from the accumulation of genetic abnormalities in the cells. Human baculoviral inhibitor of apoptosis repeat-containing 5 (BIRC5), encodes survivin, is one of only a handful of genes that is differentially over-expressed in numerous malignant diseases including AML.&lt;h4>Methods&lt;/h4>The BIRC5 was silenced permanently in two AML cell lines, HL‑60 and KG-1, via the CRISPR/Cas9n system. After transfection of CRISPR constructs, genomic DNA was extracted and amplified to assess mutation detection. To evaluate BIRC5 gene expression, quantitative real-time PCR was performed. Also, MTT cell viability and Annexin‑V/propidium iodide flowcytometric staining were performed, and the data were analyzed using the Kolmogorov</pubmed_abstract><journal>Iranian biomedical journal</journal><pagination>369-78</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6800533</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>BIRC5 Gene Disruption via CRISPR/Cas9n Platform Suppress Acute Myelocytic Leukemia Progression</pubmed_title><pmcid>PMC6800533</pmcid><pubmed_authors>Roshani D</pubmed_authors><pubmed_authors>Sharifi M</pubmed_authors><pubmed_authors>Hejazi SH</pubmed_authors><pubmed_authors>Narimani M</pubmed_authors><pubmed_authors>Jalili A</pubmed_authors><pubmed_authors>Kazemi M</pubmed_authors><pubmed_authors>Hakhamaneshi MS</pubmed_authors></additional><is_claimable>false</is_claimable><name>BIRC5 Gene Disruption via CRISPR/Cas9n Platform Suppress Acute Myelocytic Leukemia Progression</name><description>&lt;h4>Background&lt;/h4>Acute myelocytic leukemia (AML) is a clonal malignancy resulting from the accumulation of genetic abnormalities in the cells. Human baculoviral inhibitor of apoptosis repeat-containing 5 (BIRC5), encodes survivin, is one of only a handful of genes that is differentially over-expressed in numerous malignant diseases including AML.&lt;h4>Methods&lt;/h4>The BIRC5 was silenced permanently in two AML cell lines, HL‑60 and KG-1, via the CRISPR/Cas9n system. After transfection of CRISPR constructs, genomic DNA was extracted and amplified to assess mutation detection. To evaluate BIRC5 gene expression, quantitative real-time PCR was performed. Also, MTT cell viability and Annexin‑V/propidium iodide flowcytometric staining were performed, and the data were analyzed using the Kolmogorov</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Nov</publication><modification>2025-04-18T20:03:38.403Z</modification><creation>2025-04-07T07:49:21.315Z</creation></dates><accession>S-EPMC6800533</accession><cross_references><pubmed>31104397</pubmed></cross_references></HashMap>