PMID- 35778526 OWN - NLM STAT- MEDLINE DCOM- 20220707 LR - 20220909 IS - 2045-2322 (Electronic) IS - 2045-2322 (Linking) VI - 12 IP - 1 DP - 2022 Jul 1 TI - Identification of pyroptosis-related long non-coding RNAs with prognosis and therapy in lung squamous cell carcinoma. PG - 11206 LID - 10.1038/s41598-022-15373-6 [doi] LID - 11206 AB - Pyroptosis is a type of programmed cell death with an intense inflammatory response. Previous studies have shown that pyroptosis plays an important role in the pathogenesis and progression of lung cancer. However, the prognostic value and drug targets of pyroptosis-related lncRNAs in lung squamous cell carcinoma (LSCC) have never been studied. In the present study, we identified 1468 pyroptosis-related lncRNAs in LSCC by performing Pearson correlation analysis between the pyroptosis-related genes and the lncRNAs from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) database. The whole set was divided into a training and a test set with a 1:1 ratio. Univariate Cox regression and least absolute shrinkage and selection operator (LASSO) analyses were conducted to establish an 11 multilncRNA signature in the three sets. The signature divided LSCC patients into the low-risk and the high-risk groups. Kaplan-Meier analysis and receiver operating characteristic (ROC) indicated that the prognostic signature had a promising predictive capability for LSCC patients. Besides, the association of microenvironment and immunotherapy response with signature was also analyzed. Moreover, 28 potential compounds targeting signature were screened as possible drugs to treat LSCC. Finally, a nomogram model was constructed to offer the quantitative prediction and net benefit for the prognosis of LSCC patients. In conclusion, the 11 pyroptosis-related lncRNAs and their signature may be promising prognostic factors and therapeutic targets for patients with LSCC. CI - (c) 2022. The Author(s). FAU - Zhang, Yi AU - Zhang Y AD - Shengli Clinical Medical College of Fujian Medical University, Fuzhou, 350001, Fujian, People's Republic of China. FAU - Wang, Yuzhi AU - Wang Y AD - Department of Laboratory Medicine, People's Hospital of Deyang City, Deyang, 618000, Sichuan, People's Republic of China. FAU - Yin, Xiaoqing AU - Yin X AD - Fujian University of Traditional Chinese Medicine, Fuzhou, 350001, Fujian, People's Republic of China. FAU - Huang, Yi AU - Huang Y AD - Shengli Clinical Medical College of Fujian Medical University, Fuzhou, 350001, Fujian, People's Republic of China. hyi8070@126.com. AD - Department of Clinical Laboratory, Fujian Provincial Hospital, Fuzhou, 350001, Fujian, People's Republic of China. hyi8070@126.com. AD - Center for Experimental Research in Clinical Medicine, Fujian Provincial Hospital, Fuzhou, 350001, Fujian, People's Republic of China. hyi8070@126.com. AD - Central Laboratory, Fujian Provincial Hospital, Fuzhou, 350001, Fujian, People's Republic of China. hyi8070@126.com. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20220701 PL - England TA - Sci Rep JT - Scientific reports JID - 101563288 RN - 0 (Biomarkers, Tumor) RN - 0 (RNA, Long Noncoding) SB - IM MH - Biomarkers, Tumor/genetics/metabolism MH - *Carcinoma, Non-Small-Cell Lung/genetics MH - *Carcinoma, Squamous Cell/drug therapy/genetics MH - Gene Expression Regulation, Neoplastic MH - Humans MH - Lung/pathology MH - *Lung Neoplasms/drug therapy/genetics MH - Prognosis MH - Pyroptosis/genetics MH - *RNA, Long Noncoding/genetics/metabolism MH - Tumor Microenvironment/genetics PMC - PMC9249737 COIS- The authors declare no competing interests. EDAT- 2022/07/02 06:00 MHDA- 2022/07/08 06:00 PMCR- 2022/07/01 CRDT- 2022/07/01 23:26 PHST- 2022/01/11 00:00 [received] PHST- 2022/06/23 00:00 [accepted] PHST- 2022/07/01 23:26 [entrez] PHST- 2022/07/02 06:00 [pubmed] PHST- 2022/07/08 06:00 [medline] PHST- 2022/07/01 00:00 [pmc-release] AID - 10.1038/s41598-022-15373-6 [pii] AID - 15373 [pii] AID - 10.1038/s41598-022-15373-6 [doi] PST - epublish SO - Sci Rep. 2022 Jul 1;12(1):11206. doi: 10.1038/s41598-022-15373-6.