001     119276
005     20240228145431.0
024 7 _ |2 doi
|a 10.18632/oncotarget.13540
024 7 _ |2 pmid
|a pmid:27894094
037 _ _ |a DKFZ-2017-00062
041 _ _ |a eng
082 _ _ |a 610
100 1 _ |0 P:(DE-HGF)0
|a Macher-Goeppinger, Stephan
|b 0
|e First author
245 _ _ |a MET expression and copy number status in clear-cell renal cell carcinoma: prognostic value and potential predictive marker.
260 _ _ |a [S.l.]
|b Impact Journals LLC
|c 2017
336 7 _ |2 DRIVER
|a article
336 7 _ |2 DataCite
|a Output Types/Journal article
336 7 _ |0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
|a Journal Article
|b journal
|m journal
|s 1511273785_9860
336 7 _ |2 BibTeX
|a ARTICLE
336 7 _ |2 ORCID
|a JOURNAL_ARTICLE
336 7 _ |0 0
|2 EndNote
|a Journal Article
520 _ _ |a Multiple targeted therapy for advanced clear-cell renal cell carcinoma (RCC) has substantially improved patient outcome, but complete remission is uncommon and many tumors eventually develop resistance. Mechanistic, preclinical, and early clinical data highlight c-Met / hepatocyte growth factor receptor as a promising target for RCC therapeutic agents.We have examined MET expression, frequency of MET gene copy gains and MET gene mutation in a large, hospital-based series of renal cell carcinomas with long-term follow-up information.Out of a total of 572 clear-cell RCC, only 17% were negative for MET expression whereas 32% showed high protein levels. High MET expression and MET copy number gains were associated with an aggressive phenotype and an unfavorable patient outcome. Elevated protein levels in absence of gene amplification were not attributed to mutations, based on results of targeted next-generation sequencing.Our data reveal that clear-cell RCC with MET upregulation show an aggressive behavior and MET copy number increase is evident in a substantial percentage of patients with high-grade carcinomas and metastatic disease. Diagnostic assessment of MET expression and amplification may be of predictive value to guide targeted therapy against MET signaling in patients with clear-cell RCC.
536 _ _ |0 G:(DE-HGF)POF3-317
|a 317 - Translational cancer research (POF3-317)
|c POF3-317
|f POF III
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed,
700 1 _ |0 P:(DE-He78)8dd9fa632ca161d0ca1929a4d99cbe77
|a Keith, Martina
|b 1
|u dkfz
700 1 _ |a Endris, Volker
|b 2
700 1 _ |a Penzel, Roland
|b 3
700 1 _ |0 P:(DE-He78)55bdae24f65a1c0e58c6d721e968c3f4
|a Tagscherer, Katrin
|b 4
|u dkfz
700 1 _ |a Pahernik, Sascha
|b 5
700 1 _ |a Hohenfellner, Markus
|b 6
700 1 _ |a Gardner, Humphrey
|b 7
700 1 _ |a Grüllich, Carsten
|b 8
700 1 _ |a Schirmacher, Peter
|b 9
700 1 _ |0 P:(DE-He78)6c54d919bb3371b6d7f277e2c6262a4a
|a Roth, Wilfried
|b 10
|e Last author
|u dkfz
773 _ _ |0 PERI:(DE-600)2560162-3
|a 10.18632/oncotarget.13540
|g Vol. 8, no. 1
|n 1
|p 1046-1057
|t OncoTarget
|v 8
|x 1949-2553
|y 2017
909 C O |o oai:inrepo02.dkfz.de:119276
|p VDB
910 1 _ |0 I:(DE-588b)2036810-0
|6 P:(DE-HGF)0
|a Deutsches Krebsforschungszentrum
|b 0
|k DKFZ
910 1 _ |0 I:(DE-588b)2036810-0
|6 P:(DE-He78)8dd9fa632ca161d0ca1929a4d99cbe77
|a Deutsches Krebsforschungszentrum
|b 1
|k DKFZ
910 1 _ |0 I:(DE-588b)2036810-0
|6 P:(DE-He78)55bdae24f65a1c0e58c6d721e968c3f4
|a Deutsches Krebsforschungszentrum
|b 4
|k DKFZ
910 1 _ |0 I:(DE-588b)2036810-0
|6 P:(DE-He78)6c54d919bb3371b6d7f277e2c6262a4a
|a Deutsches Krebsforschungszentrum
|b 10
|k DKFZ
913 1 _ |0 G:(DE-HGF)POF3-317
|1 G:(DE-HGF)POF3-310
|2 G:(DE-HGF)POF3-300
|a DE-HGF
|l Krebsforschung
|v Translational cancer research
|x 0
|4 G:(DE-HGF)POF
|3 G:(DE-HGF)POF3
|b Gesundheit
914 1 _ |y 2017
915 _ _ |0 StatID:(DE-HGF)0100
|2 StatID
|a JCR
|b ONCOTARGET : 2015
915 _ _ |0 StatID:(DE-HGF)0200
|2 StatID
|a DBCoverage
|b SCOPUS
915 _ _ |0 StatID:(DE-HGF)0300
|2 StatID
|a DBCoverage
|b Medline
915 _ _ |0 StatID:(DE-HGF)0310
|2 StatID
|a DBCoverage
|b NCBI Molecular Biology Database
915 _ _ |0 StatID:(DE-HGF)0199
|2 StatID
|a DBCoverage
|b Thomson Reuters Master Journal List
915 _ _ |0 StatID:(DE-HGF)0111
|2 StatID
|a WoS
|b Science Citation Index Expanded
915 _ _ |0 StatID:(DE-HGF)0150
|2 StatID
|a DBCoverage
|b Web of Science Core Collection
915 _ _ |0 StatID:(DE-HGF)1050
|2 StatID
|a DBCoverage
|b BIOSIS Previews
915 _ _ |0 StatID:(DE-HGF)9905
|2 StatID
|a IF >= 5
|b ONCOTARGET : 2015
920 1 _ |0 I:(DE-He78)G150-20160331
|k G150
|l Molekulare Tumorpathologie
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)G150-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21