<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Huang H</submitter><funding>Natural Science Foundation of Tianjin City</funding><funding>National Natural Science Foundation of China</funding><pagination>850943</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8924059</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Pyroptosis is a new type of programmed cell death, accompanied by an intense inflammatory response. Previous studies have shown that pyroptosis can modify long-chain non-coding RNA (lncRNA), thereby affecting the occurrence and progression of tumors. However, the underlying role of pyroptosis-related lncRNA in lung adenocarcinoma (LUAD) remains to be elucidated. Therefore, the purpose of our study was to evaluate the prognostic value of pyrolysis-related lncRNA in patients with LUAD.&lt;h4>Methods&lt;/h4>A total of 454 LUAD samples were downloaded from The Cancer Genome Atlas (TCGA) database. Pearson's correlation coefficient was used to identify the pyroptosis-related lncRNAs. Unsupervised consensus clustering was used to identify the various LUAD molecular subtypes. A least absolute shrinkage and selection operator (LASSO) analysis was conducted to construct a prognostic signature.&lt;h4>Results&lt;/h4>An 11-lncRNA prognostic signature out of 19 identified pyroptosis-related prognostic lncRNAs was constructed. The patients with LUAD were divided into low-risk and high-risk groups. Patients in the high-risk group had higher score values and mortality. The immune score, stromal score, and estimate score were lower in the high-risk group. The risk score was an independent predictor for OS in multivariate Cox regression analyses (HR > 1, p &lt; 0.01). BTLA, PD-1, PD-L1, CTLA, and CD47 were lower expressed in the high-risk group.&lt;h4>Conclusions&lt;/h4>Our study identified an 11-pyroptosis-related lncRNA signature. These findings could further clarify the role of pyroptosis in LUAD and guide the prognosis and individualized treatment of patients.</pubmed_abstract><journal>Frontiers in oncology</journal><pubmed_title>Pyroptosis-Related LncRNA Signatures Correlate With Lung Adenocarcinoma Prognosis.</pubmed_title><pmcid>PMC8924059</pmcid><funding_grant_id>19YFZCSY00040, 19JCYBJC27000</funding_grant_id><funding_grant_id>82072595, 82172569, 81773207 , and 61973232</funding_grant_id><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Pan Z</pubmed_authors><pubmed_authors>Shi R</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Huang H</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Su L</pubmed_authors><pubmed_authors>Zhu G</pubmed_authors><pubmed_authors>Shi Z</pubmed_authors><pubmed_authors>Chen C</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Cao P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pyroptosis-Related LncRNA Signatures Correlate With Lung Adenocarcinoma Prognosis.</name><description>&lt;h4>Background&lt;/h4>Pyroptosis is a new type of programmed cell death, accompanied by an intense inflammatory response. Previous studies have shown that pyroptosis can modify long-chain non-coding RNA (lncRNA), thereby affecting the occurrence and progression of tumors. However, the underlying role of pyroptosis-related lncRNA in lung adenocarcinoma (LUAD) remains to be elucidated. Therefore, the purpose of our study was to evaluate the prognostic value of pyrolysis-related lncRNA in patients with LUAD.&lt;h4>Methods&lt;/h4>A total of 454 LUAD samples were downloaded from The Cancer Genome Atlas (TCGA) database. Pearson's correlation coefficient was used to identify the pyroptosis-related lncRNAs. Unsupervised consensus clustering was used to identify the various LUAD molecular subtypes. A least absolute shrinkage and selection operator (LASSO) analysis was conducted to construct a prognostic signature.&lt;h4>Results&lt;/h4>An 11-lncRNA prognostic signature out of 19 identified pyroptosis-related prognostic lncRNAs was constructed. The patients with LUAD were divided into low-risk and high-risk groups. Patients in the high-risk group had higher score values and mortality. The immune score, stromal score, and estimate score were lower in the high-risk group. The risk score was an independent predictor for OS in multivariate Cox regression analyses (HR > 1, p &lt; 0.01). BTLA, PD-1, PD-L1, CTLA, and CD47 were lower expressed in the high-risk group.&lt;h4>Conclusions&lt;/h4>Our study identified an 11-pyroptosis-related lncRNA signature. These findings could further clarify the role of pyroptosis in LUAD and guide the prognosis and individualized treatment of patients.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-06-18T08:50:51.116Z</modification><creation>2025-04-19T09:24:07.413Z</creation></dates><accession>S-EPMC8924059</accession><cross_references><pubmed>35311148</pubmed><doi>10.3389/fonc.2022.850943</doi></cross_references></HashMap>