Integration of single-cell transcriptomics and bulk transcriptomics to explore prognostic and immunotherapeutic characteristics of nucleotide metabolism in lung adenocarcinoma

被引:0
作者
Zhang, Kai [1 ,2 ]
Wang, Luyao [3 ]
Chen, Huili [4 ]
Deng, Lili [1 ]
Hu, Mengling [3 ]
Wang, Ziqiang [4 ]
Xie, Yiluo [2 ]
Lian, Chaoqun [4 ]
Wang, Xiaojing [1 ,5 ]
Zhang, Jing [3 ]
机构
[1] Bengbu Med Univ, Affiliated Hosp 1, Anhui Prov Key Lab Resp Tumor & Infect Dis, Bengbu, Peoples R China
[2] Bengbu Med Univ, Dept Clin Med, Bengbu, Peoples R China
[3] Bengbu Med Univ, Sch Life Sci, Dept Genet, Bengbu, Peoples R China
[4] Bengbu Med Univ, Res Ctr Clin Lab Sci, Bengbu, Peoples R China
[5] Bengbu Med Univ, Affiliated Hosp 1, Joint Res Ctr Reg Dis IHM, Bengbu, Peoples R China
关键词
lung adenocarcinoma; nucleotide metabolism; single-cell transcriptome; prognostic model; immunotherapy; CANCER; EXPRESSION; PROLIFERATION; ADENOSINE; MUTATION; COMPLEX;
D O I
10.3389/fgene.2024.1466249
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Lung adenocarcinoma (LUAD) is a highly aggressive tumor with one of the highest morbidity and mortality rates in the world. Nucleotide metabolic processes are critical for cancer development, progression, and alteration of the tumor microenvironment. However, the effect of nucleotide metabolism on LUAD remains to be thoroughly investigated.Methods Transcriptomic and clinical data of LUAD were downloaded and organized from TCGA and GEO databases. Genes related to nucleotide metabolism were downloaded from the Msigdb database. Genes associated with LUAD prognosis were identified using univariate COX analysis, and a prognostic risk model was constructed using the machine learning combination of Lasso + Stepcox. The model's predictive validity was evaluated using KM survival and timeROC curves. Based on the prognostic model, LUAD patients were classified into different nucleotide metabolism subtypes, and the differences between patients of different subtypes were explored in terms of genomic mutations, functional enrichment, tumor immune characteristics, and immunotherapy responses. Finally, the key gene SNRPA was screened, and a series of in vitro experiments were performed on LUAD cell lines to explore the role of SNRPA in LUAD.Result LUAD patients could be accurately categorized into subtypes based on the nucleotide metabolism-related prognostic risk score (NMBRS). There were significant differences in prognosis between patients of different subtypes, and the NMBRS showed high accuracy in predicting the prognosis of LUAD patients. In addition, patients of different subtypes showed significant differences in genomic mutation and functional enrichment and exhibited different anti-tumor immune profiles. Importantly, NMBRS can be used to predict the responsiveness of LUAD patients to immunotherapy. The results of in vitro cellular experiments indicate that SNRPA plays an important role in the development and progression of lung adenocarcinoma.Conclusion This study comprehensively reveals the prognostic value and clinical application of nucleotide metabolism in LUAD. A prognostic signature constructed based on genes related to nucleotide metabolism accurately predicted the prognosis of LUAD patients, and this signature can be used as a guide for LUAD immunotherapy.
引用
收藏
页数:21
相关论文
共 61 条
[1]  
Aibar S, 2017, NAT METHODS, V14, P1083, DOI [10.1038/NMETH.4463, 10.1038/nmeth.4463]
[2]   Adenosine signaling and the immune system: When a lot could be too much [J].
Antonioli, Luca ;
Fornai, Matteo ;
Blandizzi, Corrado ;
Pacher, Pal ;
Hasko, Gyorgy .
IMMUNOLOGY LETTERS, 2019, 205 :9-15
[3]   VEGF in Signaling and Disease: Beyond Discovery and Development [J].
Apte, Rajendra S. ;
Chen, Daniel S. ;
Ferrara, Napoleone .
CELL, 2019, 176 (06) :1248-1264
[4]   Reference-based analysis of lung single-cell sequencing reveals a transitional profibrotic macrophage [J].
Aran, Dvir ;
Looney, Agnieszka P. ;
Liu, Leqian ;
Wu, Esther ;
Fong, Valerie ;
Hsu, Austin ;
Chak, Suzanna ;
Naikawadi, Ram P. ;
Wolters, Paul J. ;
Abate, Adam R. ;
Butte, Atul J. ;
Bhattacharya, Mallar .
NATURE IMMUNOLOGY, 2019, 20 (02) :163-+
[5]   Conserved pan-cancer microenvironment subtypes predict response to immunotherapy [J].
Bagaev, Alexander ;
Kotlov, Nikita ;
Nomie, Krystle ;
Svekolkin, Viktor ;
Gafurov, Azamat ;
Isaeva, Olga ;
Osokin, Nikita ;
Kozlov, Ivan ;
Frenkel, Felix ;
Gancharova, Olga ;
Almog, Nava ;
Tsiper, Maria ;
Ataullakhanov, Ravshan ;
Fowler, Nathan .
CANCER CELL, 2021, 39 (06) :845-+
[6]   U1 small nuclear ribonucleoprotein complex and RNA splicing alterations in Alzheimer's disease [J].
Bai, Bing ;
Hales, Chadwick M. ;
Chen, Ping-Chung ;
Gozal, Yair ;
Dammer, Eric B. ;
Fritz, Jason J. ;
Wang, Xusheng ;
Xia, Qiangwei ;
Duong, Duc M. ;
Street, Craig ;
Cantero, Gloria ;
Cheng, Dongmei ;
Jones, Drew R. ;
Wu, Zhiping ;
Li, Yuxin ;
Diner, Ian ;
Heilman, Craig J. ;
Rees, Howard D. ;
Wu, Hao ;
Lin, Li ;
Szulwach, Keith E. ;
Gearing, Marla ;
Mufson, Elliott J. ;
Bennett, David A. ;
Montine, Thomas J. ;
Seyfried, Nicholas T. ;
Wingo, Thomas S. ;
Sun, Yi E. ;
Jin, Peng ;
Hanfelt, John ;
Willcock, Donna M. ;
Levey, Allan ;
Lah, James J. ;
Peng, Junmin .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (41) :16562-16567
[7]   Atezolizumab as first-line treatment in cisplatin-ineligible patients with locally advanced and metastatic urothelial carcinoma: a single-arm, multicentre, phase 2 trial [J].
Balar, Arjun V. ;
Galsky, Matthew D. ;
Rosenberg, Jonathan E. ;
Powles, Thomas ;
Petrylak, Daniel P. ;
Bellmunt, Joaquim ;
Loriot, Yohann ;
Necchi, Andrea ;
Hoffman-Censits, Jean ;
Perez-Gracia, Jose Luis ;
Dawson, Nancy A. ;
van der Heijden, Michiel S. ;
Dreicer, Robert ;
Srinivas, Sandy ;
Retz, Margitta M. ;
Joseph, Richard W. ;
Drakaki, Alexandra ;
Vaishampayan, Ulka N. ;
Sridhar, Srikala S. ;
Quinn, David I. ;
Duran, Ignacio ;
Shaffer, David R. ;
Eigl, Bernhard J. ;
Grivas, Petros D. ;
Yu, Evan Y. ;
Li, Shi ;
Kadel, Edward E., III ;
Boyd, Zachary ;
Bourgon, Richard ;
Hegde, Priti S. ;
Mariathasan, Sanjeev ;
Thastrom, AnnChristine ;
Abidoye, Oyewale O. ;
Fine, Gregg D. ;
Bajorin, Dean F. .
LANCET, 2017, 389 (10064) :67-76
[8]   Single-cell RNA sequencing reveals distinct tumor microenvironmental patterns in lung adenocarcinoma [J].
Bischoff, Philip ;
Trinks, Alexandra ;
Obermayer, Benedikt ;
Pett, Jan Patrick ;
Wiederspahn, Jennifer ;
Uhlitz, Florian ;
Liang, Xizi ;
Lehmann, Annika ;
Jurmeister, Philipp ;
Elsner, Aron ;
Dziodzio, Tomasz ;
Rueckert, Jens-Carsten ;
Neudecker, Jens ;
Falk, Christine ;
Beule, Dieter ;
Sers, Christine ;
Morkel, Markus ;
Horst, David ;
Bluethgen, Nils ;
Klauschen, Frederick .
ONCOGENE, 2021, 40 (50) :6748-6758
[9]   The Society for Immunotherapy of Cancer consensus statement on immunotherapy for the treatment of non-small cell lung cancer (NSCLC) [J].
Brahmer, Julie R. ;
Govindan, Ramaswamy ;
Anders, Robert A. ;
Antonia, Scott J. ;
Sagorsky, Sarah ;
Davies, Marianne J. ;
Dubinett, Steven M. ;
Ferris, Andrea ;
Gandhi, Leena ;
Garon, Edward B. ;
Hellmann, Matthew D. ;
Hirsch, Fred R. ;
Malik, Shakuntala ;
Neal, Joel W. ;
Papadimitrakopoulou, Vassiliki A. ;
Rimm, David L. ;
Schwartz, Lawrence H. ;
Sepesi, Boris ;
Yeap, Beow Yong ;
Rizvi, Naiyer A. ;
Herbst, Roy S. .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2018, 6
[10]   Pan-cancer Immunogenomic Analyses Reveal Genotype-Immunophenotype Relationships and Predictors of Response to Checkpoint Blockade [J].
Charoentong, Pornpimol ;
Finotello, Francesca ;
Angelova, Mihaela ;
Mayer, Clemens ;
Efremova, Mirjana ;
Rieder, Dietmar ;
Hackl, Hubert ;
Trajanoski, Zlatko .
CELL REPORTS, 2017, 18 (01) :248-262