<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(1)</volume><submitter>Tseng YH</submitter><pubmed_abstract>TP53 mutations are recognized to correlate with a worse prognosis in individuals with non-small cell lung cancer (NSCLC). There exists an immediate necessity to pinpoint selective treatment for patients carrying TP53 mutations. Potential drugs were identified by comparing drug sensitivity differences, represented by the half-maximal inhibitory concentration (IC50), between TP53 mutant and wild-type NSCLC cell lines using database analysis. In addition, clinical data from NSCLC patients were collected to evaluate both their TP53 status and their response to gemcitabine, thereby facilitating further validation. Subsequently, NSCLC cell lines with different TP53 status (A549 and H1299) were subjected to gemcitabine treatment to investigate the association between TP53 mutations and gemcitabin</pubmed_abstract><journal>Cell death discovery</journal><pagination>26</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11772833</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Utilizing TP53 hotspot mutations as effective predictors of gemcitabine treatment outcome in non-small-cell lung cancer.</pubmed_title><pmcid>PMC11772833</pmcid><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Chang IY</pubmed_authors><pubmed_authors>Hsieh HW</pubmed_authors><pubmed_authors>Nguyen AT</pubmed_authors><pubmed_authors>Huang CF</pubmed_authors><pubmed_authors>Huang TY</pubmed_authors><pubmed_authors>Chang YC</pubmed_authors><pubmed_authors>Chang PM</pubmed_authors><pubmed_authors>Tsai Chang J</pubmed_authors><pubmed_authors>Tran TTM</pubmed_authors><pubmed_authors>Tseng YH</pubmed_authors><pubmed_authors>Chen YT</pubmed_authors><pubmed_authors>Juang YL</pubmed_authors><pubmed_authors>Chen YM</pubmed_authors><pubmed_authors>Huang YT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Utilizing TP53 hotspot mutations as effective predictors of gemcitabine treatment outcome in non-small-cell lung cancer.</name><description>TP53 mutations are recognized to correlate with a worse prognosis in individuals with non-small cell lung cancer (NSCLC). There exists an immediate necessity to pinpoint selective treatment for patients carrying TP53 mutations. Potential drugs were identified by comparing drug sensitivity differences, represented by the half-maximal inhibitory concentration (IC50), between TP53 mutant and wild-type NSCLC cell lines using database analysis. In addition, clinical data from NSCLC patients were collected to evaluate both their TP53 status and their response to gemcitabine, thereby facilitating further validation. Subsequently, NSCLC cell lines with different TP53 status (A549 and H1299) were subjected to gemcitabine treatment to investigate the association between TP53 mutations and gemcitabin</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2025-07-10T03:08:57.396Z</modification><creation>2025-04-04T22:21:52.593Z</creation></dates><accession>S-EPMC11772833</accession><cross_references><pubmed>39870629</pubmed><doi>10.1038/s41420-025-02300-7</doi></cross_references></HashMap>