Matches in SemOpenAlex for { <https://semopenalex.org/work/W2742760452> ?p ?o ?g. }
- W2742760452 endingPage "2219" @default.
- W2742760452 startingPage "2210" @default.
- W2742760452 abstract "The protease degradome is defined as the complete repertoire of proteases and inhibitors, and their nonfunctional homologs present in a cell, tissue or organism at any given time. We review the tissue distribution of virtually the entire degradome in 23 different human tissues and 6 ovarian cancer cell lines. To do so, we developed the CLIP-CHIP™, a custom microarray based on a 70-mer oligonucleotide platform, to specifically profile the transcripts of the entire repertoire of 473 active human proteases, 156 protease inhibitors and 92 non-proteolytically active homologs known at the design date using one specific 70-mer oligonucleotide per transcript. Using the CLIP-CHIP™ we mapped the expression profile of proteases and their inhibitors in 23 different human tissues and 6 ovarian cancer cell lines in 104 sample datasets. Hierarchical cluster analysis showed that expression profiles clustered according to their anatomic locations, cellular composition, physiologic functions, and the germ layer from which they are derived. The human ovarian cancer cell lines cluster according to malignant grade. 110 proteases and 42 inhibitors were tissue specific (1 to 3 tissues). Of these 110 proteases 69% (74) are mainly extracellular, 30% (34) intracellular and 1% intramembrane. Notably, 35% (197/565) of human proteases and 30% (47/156) of inhibitors were ubiquitously expressed in all 23 tissues; 27% (155) of proteases and 21% (32) of inhibitors were broadly expressed in 4-20 tissues. Our datasets provide a valuable resource for the community of baseline protease and inhibitor relative expression in normal human tissues and can be used for comparison with diseased tissue, e.g. ovarian cancer, to decipher pathogenesis, and to aid drug development. This article is part of a Special Issue entitled: Proteolysis as a Regulatory Event in Pathophysiology edited by Stefan Rose-John." @default.
- W2742760452 created "2017-08-17" @default.
- W2742760452 creator A5022308392 @default.
- W2742760452 creator A5043803485 @default.
- W2742760452 creator A5053252393 @default.
- W2742760452 creator A5085818807 @default.
- W2742760452 creator A5087974982 @default.
- W2742760452 creator A5091420701 @default.
- W2742760452 date "2017-11-01" @default.
- W2742760452 modified "2023-10-18" @default.
- W2742760452 title "Overview of transcriptomic analysis of all human proteases, non-proteolytic homologs and inhibitors: Organ, tissue and ovarian cancer cell line expression profiling of the human protease degradome by the CLIP-CHIP™ DNA microarray" @default.
- W2742760452 cites W1504163891 @default.
- W2742760452 cites W1965179332 @default.
- W2742760452 cites W1978591675 @default.
- W2742760452 cites W1979338861 @default.
- W2742760452 cites W1991380003 @default.
- W2742760452 cites W2005759392 @default.
- W2742760452 cites W2007810290 @default.
- W2742760452 cites W2010912389 @default.
- W2742760452 cites W2016345267 @default.
- W2742760452 cites W2028277256 @default.
- W2742760452 cites W2044841261 @default.
- W2742760452 cites W2046582315 @default.
- W2742760452 cites W2047979760 @default.
- W2742760452 cites W2051239163 @default.
- W2742760452 cites W2057560702 @default.
- W2742760452 cites W2062919894 @default.
- W2742760452 cites W2068843202 @default.
- W2742760452 cites W2069508712 @default.
- W2742760452 cites W2075503331 @default.
- W2742760452 cites W2076757423 @default.
- W2742760452 cites W2078354424 @default.
- W2742760452 cites W2081098333 @default.
- W2742760452 cites W2087973465 @default.
- W2742760452 cites W2112238496 @default.
- W2742760452 cites W2112657854 @default.
- W2742760452 cites W2121777852 @default.
- W2742760452 cites W2131798870 @default.
- W2742760452 cites W2143717394 @default.
- W2742760452 cites W2150926065 @default.
- W2742760452 cites W2164216268 @default.
- W2742760452 cites W2501711339 @default.
- W2742760452 cites W2508475180 @default.
- W2742760452 cites W2605035492 @default.
- W2742760452 cites W2738019036 @default.
- W2742760452 cites W4294107304 @default.
- W2742760452 cites W4320800236 @default.
- W2742760452 cites W45534775 @default.
- W2742760452 doi "https://doi.org/10.1016/j.bbamcr.2017.08.004" @default.
- W2742760452 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28797648" @default.
- W2742760452 hasPublicationYear "2017" @default.
- W2742760452 type Work @default.
- W2742760452 sameAs 2742760452 @default.
- W2742760452 citedByCount "34" @default.
- W2742760452 countsByYear W27427604522018 @default.
- W2742760452 countsByYear W27427604522019 @default.
- W2742760452 countsByYear W27427604522020 @default.
- W2742760452 countsByYear W27427604522021 @default.
- W2742760452 countsByYear W27427604522022 @default.
- W2742760452 countsByYear W27427604522023 @default.
- W2742760452 crossrefType "journal-article" @default.
- W2742760452 hasAuthorship W2742760452A5022308392 @default.
- W2742760452 hasAuthorship W2742760452A5043803485 @default.
- W2742760452 hasAuthorship W2742760452A5053252393 @default.
- W2742760452 hasAuthorship W2742760452A5085818807 @default.
- W2742760452 hasAuthorship W2742760452A5087974982 @default.
- W2742760452 hasAuthorship W2742760452A5091420701 @default.
- W2742760452 hasBestOaLocation W27427604521 @default.
- W2742760452 hasConcept C104317684 @default.
- W2742760452 hasConcept C121608353 @default.
- W2742760452 hasConcept C150194340 @default.
- W2742760452 hasConcept C153911025 @default.
- W2742760452 hasConcept C162317418 @default.
- W2742760452 hasConcept C181199279 @default.
- W2742760452 hasConcept C182220744 @default.
- W2742760452 hasConcept C18431079 @default.
- W2742760452 hasConcept C2776714187 @default.
- W2742760452 hasConcept C2780427987 @default.
- W2742760452 hasConcept C54355233 @default.
- W2742760452 hasConcept C55493867 @default.
- W2742760452 hasConcept C70721500 @default.
- W2742760452 hasConcept C81885089 @default.
- W2742760452 hasConcept C86803240 @default.
- W2742760452 hasConcept C95371953 @default.
- W2742760452 hasConcept C95444343 @default.
- W2742760452 hasConceptScore W2742760452C104317684 @default.
- W2742760452 hasConceptScore W2742760452C121608353 @default.
- W2742760452 hasConceptScore W2742760452C150194340 @default.
- W2742760452 hasConceptScore W2742760452C153911025 @default.
- W2742760452 hasConceptScore W2742760452C162317418 @default.
- W2742760452 hasConceptScore W2742760452C181199279 @default.
- W2742760452 hasConceptScore W2742760452C182220744 @default.
- W2742760452 hasConceptScore W2742760452C18431079 @default.
- W2742760452 hasConceptScore W2742760452C2776714187 @default.
- W2742760452 hasConceptScore W2742760452C2780427987 @default.
- W2742760452 hasConceptScore W2742760452C54355233 @default.
- W2742760452 hasConceptScore W2742760452C55493867 @default.
- W2742760452 hasConceptScore W2742760452C70721500 @default.