<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xiong Y</submitter><funding>National Natural Science Foundation of China</funding><funding>Special Funds for the Basic Research and Development Program in the Central Non-profit Research Institutesof China</funding><pagination>499</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10369768</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>Transcriptional programs are often dysregulated in cancers. A comprehensive investigation of potential regulons is critical to the understanding of tumorigeneses. We first constructed the regulatory networks from single-cell RNA sequencing data in human lung adenocarcinoma (LUAD). We next introduce LPRI (Lung Cancer Prognostic Regulon Index), a precision oncology framework to identify new biomarkers associated with prognosis by leveraging the single cell regulon atlas and bulk RNA sequencing or microarray datasets. We confirmed that LPRI could be a robust biomarker to guide prognosis stratification across lung adenocarcinoma cohorts. Finally, a multi-omics data analysis to characterize molecular alterations associated with LPRI was performed from The Cancer Genome Atlas (TCGA) dataset. Our</pubmed_abstract><journal>Journal of translational medicine</journal><pubmed_title>Integration of single-cell regulon atlas and multi-omics data for prognostic stratification and personalized treatment prediction in human lung adenocarcinoma.</pubmed_title><pmcid>PMC10369768</pmcid><funding_grant_id>81770781</funding_grant_id><funding_grant_id>82270825</funding_grant_id><funding_grant_id>2020SK2062</funding_grant_id><funding_grant_id>81472594</funding_grant_id><pubmed_authors>Xiong Y</pubmed_authors><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Xia Z</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Liu N</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Yang Q</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Wanggou S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Integration of single-cell regulon atlas and multi-omics data for prognostic stratification and personalized treatment prediction in human lung adenocarcinoma.</name><description>Transcriptional programs are often dysregulated in cancers. A comprehensive investigation of potential regulons is critical to the understanding of tumorigeneses. We first constructed the regulatory networks from single-cell RNA sequencing data in human lung adenocarcinoma (LUAD). We next introduce LPRI (Lung Cancer Prognostic Regulon Index), a precision oncology framework to identify new biomarkers associated with prognosis by leveraging the single cell regulon atlas and bulk RNA sequencing or microarray datasets. We confirmed that LPRI could be a robust biomarker to guide prognosis stratification across lung adenocarcinoma cohorts. Finally, a multi-omics data analysis to characterize molecular alterations associated with LPRI was performed from The Cancer Genome Atlas (TCGA) dataset. Our</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jul</publication><modification>2025-04-05T12:36:18.198Z</modification><creation>2025-04-05T12:36:18.198Z</creation></dates><accession>S-EPMC10369768</accession><cross_references><pubmed>37491302</pubmed><doi>10.1186/s12967-023-04331-z</doi></cross_references></HashMap>