INT113568

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Context Info
Confidence 0.94
First Reported 2003
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 5
Total Number 5
Disease Relevance 4.79
Pain Relevance 0.57

This is a graph with borders and nodes. Maybe there is an Imagemap used so the nodes may be linking to some Pages.

peptidase activity (PLAU) signal transduction (PLAU) extracellular space (PLAU)
extracellular region (PLAU) plasma membrane (PLAU)
Anatomy Link Frequency
extracellular matrix 4
vessels 1
PLAU (Homo sapiens)
Pain Link Frequency Relevance Heat
chemokine 1 94.56 High High
metalloproteinase 76 89.20 High High
Inflammation 6 87.84 High High
cytokine 3 84.24 Quite High
aspirin 10 75.00 Quite High
COX-2 inhibitor 25 70.64 Quite High
cINOD 3 65.68 Quite High
methotrexate 1 46.80 Quite Low
COX2 2 5.00 Very Low Very Low Very Low
palliative 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Metastasis 38 100.00 Very High Very High Very High
Cancer 174 98.92 Very High Very High Very High
Advanced Or Metastatic Breast Cancer 5 98.40 Very High Very High Very High
Adhesions 5 96.68 Very High Very High Very High
Wound Healing 6 96.60 Very High Very High Very High
Breast Cancer 114 91.52 High High
Disease 10 88.28 High High
INFLAMMATION 8 87.84 High High
Prostate Cancer 7 75.00 Quite High
Injury 15 65.20 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
In addition to the proteolytic activity of uPA, which degrades the extracellular matrix, uPA also binds to its receptor (uPAR) and controls cell adhesion and migration through the reorganization of actin cytoskeleton.
Protein_catabolism (degrades) of uPA in extracellular matrix associated with adhesions
1) Confidence 0.94 Published 2003 Journal Int. J. Oncol. Section Abstract Doc Link 14532966 Disease Relevance 0.82 Pain Relevance 0.16
In turn, de novo formed vessels strengthen tumour invasion and metastasis through the production of MMP 2 and 9 and uPA, which further degrade ECM.
Protein_catabolism (degrade) of uPA in vessels associated with cancer and metastasis
2) Confidence 0.35 Published 2010 Journal BMC Cancer Section Body Doc Link PMC2841144 Disease Relevance 0.99 Pain Relevance 0
For example, uPA, uPAR and its inhibitor PAI-1 are responsible for the degradation and remodeling of the extracellular matrix, and are further involved in angiogenesis, cell adhesion and migration necessary for tumor cell invasion and metastasis [31,32].
Protein_catabolism (degradation) of uPA in extracellular matrix associated with cancer, metastasis and adhesions
3) Confidence 0.29 Published 2006 Journal Breast Cancer Res Section Body Doc Link PMC1779463 Disease Relevance 1.25 Pain Relevance 0.21
The urokinase-type plasminogen activator (uPA) is a serine protease that plays an important role in the invasion and metastasis process through degradation of the extracellular matrix.
Protein_catabolism (degradation) of uPA in extracellular matrix associated with metastasis
4) Confidence 0.24 Published 2004 Journal Breast Cancer Res Section Body Doc Link PMC400674 Disease Relevance 0.88 Pain Relevance 0
The uPA activates proteases and MMPs that degrade the basement membrane and mediate cytoskeleton reorganization. [6,12,14].
Protein_catabolism (degrade) of uPA in basement membrane
5) Confidence 0.12 Published 2006 Journal BMC Cancer Section Body Doc Link PMC1559713 Disease Relevance 0.86 Pain Relevance 0.19

General Comments

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