<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8</volume><submitter>Chen J</submitter><pubmed_abstract>Metformin is a classic type II diabetes drug which possesses anti-tumor properties for various cancers. However, different cancers do not respond to metformin with the same effectiveness or acquire resistance. Thus, searching for vulnerabilities of metformin-resistant prostate cancer is a promising strategy to improve the therapeutic efficiency of the drug. A genome-scale CRISPR-Cas9 activation library search targeting 23,430 genes was conducted to identify the genes that confer resistance to metformin in prostate cancer cells. Candidate genes were selected by total reads of sgRNA and sgRNA diversity, and then a CCK8 assay was used to verify their resistance to metformin. Interestingly, we discovered that the activation of ECE1, ABCA12, BPY2, EEF1A1, RAD9A, and NIPSNAP1 contributed to &lt;i>i</pubmed_abstract><journal>Frontiers in cell and developmental biology</journal><pagination>616332</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7870801</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genome-Scale CRISPR-Cas9 Transcriptional Activation Screening in Metformin Resistance Related Gene of Prostate Cancer.</pubmed_title><pmcid>PMC7870801</pmcid><pubmed_authors>Liao J</pubmed_authors><pubmed_authors>Tang Z</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Ling X</pubmed_authors><pubmed_authors>Zhong W</pubmed_authors><pubmed_authors>Fang S</pubmed_authors><pubmed_authors>Yuan X</pubmed_authors><pubmed_authors>Zhou X</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Zhao H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome-Scale CRISPR-Cas9 Transcriptional Activation Screening in Metformin Resistance Related Gene of Prostate Cancer.</name><description>Metformin is a classic type II diabetes drug which possesses anti-tumor properties for various cancers. However, different cancers do not respond to metformin with the same effectiveness or acquire resistance. Thus, searching for vulnerabilities of metformin-resistant prostate cancer is a promising strategy to improve the therapeutic efficiency of the drug. A genome-scale CRISPR-Cas9 activation library search targeting 23,430 genes was conducted to identify the genes that confer resistance to metformin in prostate cancer cells. Candidate genes were selected by total reads of sgRNA and sgRNA diversity, and then a CCK8 assay was used to verify their resistance to metformin. Interestingly, we discovered that the activation of ECE1, ABCA12, BPY2, EEF1A1, RAD9A, and NIPSNAP1 contributed to &lt;i>i</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2025-04-21T17:47:59.013Z</modification><creation>2025-04-05T16:58:58.331Z</creation></dates><accession>S-EPMC7870801</accession><cross_references><pubmed>33575255</pubmed><doi>10.3389/fcell.2020.616332</doi></cross_references></HashMap>