001     289478
005     20240425122533.0
024 7 _ |a 10.1016/j.lfs.2024.122631
|2 doi
024 7 _ |a pmid:38621585
|2 pmid
024 7 _ |a 0024-3205
|2 ISSN
024 7 _ |a 0300-9653
|2 ISSN
024 7 _ |a 0300-9637
|2 ISSN
024 7 _ |a 1879-0631
|2 ISSN
037 _ _ |a DKFZ-2024-00800
041 _ _ |a English
082 _ _ |a 570
100 1 _ |a Geng, Haigang
|b 0
245 _ _ |a Targeting cellular senescence as a therapeutic vulnerability in gastric cancer.
260 _ _ |a New York, NY [u.a.]
|c 2024
|b Elsevier Science
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1714038024_1930
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
500 _ _ |a Volume 346, 1 June 2024, 122631
520 _ _ |a Cellular senescence (CS) represents an intracellular defense mechanism responding to stress signals and can be leveraged as a 'vulnerability' in cancer treatment. This study aims to construct a CS atlas for gastric cancer (GC) and uncover potential therapeutics for GC patients.38 senescence-associated regulators with prognostic significance in GC were obtained from the CellAge database to construct Gastric cancer-specific Senescence Score (GSS). Using eXtreme Sum algorism, GSS-based drug repositioning was conducted to identify drugs that could antagonize GSS in CMap database. In vitro experiments were conducted to test the effect of combination of palbociclib and exisulind in eliminating GC cells.Patients with high GSS exhibited CS-related features, such as CS markers upregulation, adverse clinical outcomes and hypomethylation status. scRNA-seq data showed malignant cells with high GSS exhibited enhanced senescence state and more immunosuppressive signals such as PVR-CD96 compared with malignant cells with low GSS. In addition, the GSS-High cancer associated fibroblasts might secrete cytokines and chemokines such as IL-6, CXCL1, CXCL12, and CCL2 to from an immunosuppressive microenvironment, and GSS could serve as an indicator for immunotherapy resistance. Exisulind exhibited the greatest potential to reverse GSS. In vitro experiments demonstrated that exisulind could induce apoptosis and suppress the proliferation of palbociclib-induced senescent GC cells.Overall, GSS offers a framework for better understanding of correlation between senescence and GC, which might provide new insights into the development of novel therapeutics in GC.
536 _ _ |a 314 - Immunologie und Krebs (POF4-314)
|0 G:(DE-HGF)POF4-314
|c POF4-314
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: inrepo02.dkfz.de
650 _ 7 |a Cellular senescence
|2 Other
650 _ 7 |a Drug repositioning
|2 Other
650 _ 7 |a Exisulind
|2 Other
650 _ 7 |a Gastric cancer
|2 Other
650 _ 7 |a Immunosuppressive microenvironment
|2 Other
650 _ 7 |a Multi-omics
|2 Other
700 1 _ |a Huang, Chen
|b 1
700 1 _ |a Xu, Lei
|b 2
700 1 _ |a Zhou, Yangyang
|b 3
700 1 _ |a Dong, Zhongyi
|b 4
700 1 _ |a Zhong, Yiqing
|b 5
700 1 _ |a Li, Qian
|b 6
700 1 _ |a Yang, Chen
|0 P:(DE-He78)8b693edfb7c78bb156cc92812eec1c55
|b 7
|u dkfz
700 1 _ |a Huang, Shaozhuo
|b 8
700 1 _ |a Liao, Weixin
|b 9
700 1 _ |a Lin, Yuxuan
|b 10
700 1 _ |a Liu, Zhicheng
|b 11
700 1 _ |a Li, Qing
|b 12
700 1 _ |a Zhang, Zizhen
|b 13
700 1 _ |a Zhu, Chunchao
|b 14
773 _ _ |a 10.1016/j.lfs.2024.122631
|g p. 122631 -
|0 PERI:(DE-600)2013911-1
|p 122631
|t Life sciences
|v 346
|y 2024
|x 0024-3205
909 C O |p VDB
|o oai:inrepo02.dkfz.de:289478
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 7
|6 P:(DE-He78)8b693edfb7c78bb156cc92812eec1c55
913 1 _ |a DE-HGF
|b Gesundheit
|l Krebsforschung
|1 G:(DE-HGF)POF4-310
|0 G:(DE-HGF)POF4-314
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Immunologie und Krebs
|x 0
914 1 _ |y 2024
915 _ _ |a Nationallizenz
|0 StatID:(DE-HGF)0420
|2 StatID
|d 2023-08-24
|w ger
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b LIFE SCI : 2022
|d 2023-08-24
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2023-08-24
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2023-08-24
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0600
|2 StatID
|b Ebsco Academic Search
|d 2023-08-24
915 _ _ |a Peer Review
|0 StatID:(DE-HGF)0030
|2 StatID
|b ASC
|d 2023-08-24
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2023-08-24
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
|d 2023-08-24
915 _ _ |a WoS
|0 StatID:(DE-HGF)0113
|2 StatID
|b Science Citation Index Expanded
|d 2023-08-24
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2023-08-24
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
|d 2023-08-24
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1190
|2 StatID
|b Biological Abstracts
|d 2023-08-24
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2023-08-24
915 _ _ |a IF >= 5
|0 StatID:(DE-HGF)9905
|2 StatID
|b LIFE SCI : 2022
|d 2023-08-24
920 1 _ |0 I:(DE-He78)D250-20160331
|k D250
|l NWG Krebs-Immunregulation
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)D250-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21