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Literature summary for 3.4.22.27 extracted from

  • Li, X.; Cheng, X.W.; Hu, L.; Wu, H.; Guo-Ping, H.; Hao, C.N.; Jiang, H.; Zhu, E.; Huang, Z.; Inoue, A.; Sasaki, T.; Du, Q.; Takeshita, K.; Okumura, K.; Murohara, T.; Kuzuya, M.
    Cathepsin S activity controls ischemia-induced neovascularization in mice (2015), Int. J. Cardiol., 183, 198-208.
    View publication on PubMed

Organism

Organism UniProt Comment Textmining
Homo sapiens P25774
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Mus musculus O70370
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Source Tissue

Source Tissue Comment Organism Textmining
HUVEC cell hypoxia increases the levels of CatS gene and protein in cultured HUVECs Homo sapiens
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Synonyms

Synonyms Comment Organism
cathepsin S
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Mus musculus
cathepsin S
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Homo sapiens

Expression

Organism Comment Expression
Homo sapiens hypoxia increases the levels of CatS gene and protein in cultured HUVECs up

General Information

General Information Comment Organism
malfunction CatS knockdown leads to defective endothelial cell invasion, proliferation, and tube formation as shown in CatS knockout mice and CatS silincing in HUVEC cells Mus musculus
malfunction silencing of CatS impairs the HUVEC invasion, proliferation and tubulogenesis Homo sapiens
physiological function CatS activity controls ischemia-induced neovascularization partially via the modulation of PPAR-gamma and VEGF/Akt signaling activation Mus musculus
physiological function CatS activity controls ischemia-induced neovascularization partially via the modulation of PPAR-gamma and VEGF/Akt signaling activation Homo sapiens