Target type: biologicalprocess
Any process that stops, prevents or reduces the frequency, rate or extent of extracellular matrix organization. [GO_REF:0000058, GOC:BHF, GOC:rl, GOC:TermGenie, PMID:22357537]
Negative regulation of extracellular matrix organization is a complex biological process that involves a variety of cellular and molecular mechanisms. It is essential for maintaining tissue homeostasis and preventing excessive deposition of extracellular matrix (ECM) components, which can lead to fibrosis and other pathological conditions.
The ECM is a dynamic network of proteins, carbohydrates, and other molecules that surrounds cells and provides structural support, regulates cell behavior, and plays a critical role in tissue development and repair. The organization of the ECM is tightly regulated by a balance of synthesis and degradation processes.
Negative regulation of ECM organization involves a variety of mechanisms, including:
- **Reduced production of ECM components:** This can be achieved by inhibiting the expression and activity of ECM synthesis enzymes, such as collagen and elastin synthases.
- **Increased degradation of ECM components:** This is accomplished by upregulating the activity of ECM-degrading enzymes, such as matrix metalloproteinases (MMPs) and other proteases.
- **Modulation of ECM assembly:** This involves altering the interactions between ECM components, which can affect the organization and stability of the ECM.
- **Regulation of cell signaling pathways:** ECM components can activate specific cell signaling pathways that regulate ECM production and degradation.
- **Control of cell behavior:** ECM organization can influence cell migration, proliferation, and differentiation.
Negative regulation of ECM organization is crucial for maintaining tissue integrity and preventing fibrosis. For example, in wound healing, ECM deposition is essential for tissue repair, but excessive ECM deposition can lead to scar formation. Similarly, in diseases such as cancer, ECM remodeling can contribute to tumor growth and metastasis.
The dysregulation of ECM organization can contribute to a variety of pathological conditions, including:
- **Fibrosis:** Excessive ECM deposition can lead to fibrosis, a condition characterized by the thickening and scarring of tissues.
- **Cancer:** ECM remodeling can promote tumor growth and metastasis.
- **Arthritis:** Degradation of articular cartilage, a specialized ECM, can contribute to arthritis.
- **Cardiovascular disease:** ECM alterations can contribute to atherosclerosis and heart failure.
Therefore, understanding the mechanisms of negative regulation of ECM organization is essential for developing therapies for a variety of diseases.'
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Protein | Definition | Taxonomy |
---|---|---|
Prolyl endopeptidase FAP | A prolyl endopeptidase FAP that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q12884] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
n-carbobenzoxyglycyl-prolyl-4-methylcoumarinyl amide | N-carbobenzoxyglycyl-prolyl-4-methylcoumarinyl amide: fluorogenic substrate for post-proline cleaving enzyme | ||
sitagliptin | sitagliptin : A triazolopyrazine that exhibits hypoglycemic activity. | triazolopyrazine; trifluorobenzene | EC 3.4.14.5 (dipeptidyl-peptidase IV) inhibitor; environmental contaminant; hypoglycemic agent; serine proteinase inhibitor; xenobiotic |
vildagliptin | amino acid amide | ||
talabostat | talabostat: an antineoplastic agent; structure in first source | ||
linagliptin | linagliptin : A xanthine that is 7H-xanthine bearing (4-methylquinazolin-2-yl)methyl, methyl, but-2-yn-1-yl and 3-aminopiperidin-1-yl substituents at positions 1, 3, 7 and 8 respectively (the R-enantiomer). Used for treatment of type II diabetes. Linagliptin: A purine and quinazoline derivative that functions as an INCRETIN and DIPEPTIDYL-PEPTIDASE IV INHIBTOR. It is used as a HYPOGLYCEMIC AGENT in the treatment of TYPE II DIABETES MELLITUS. | aminopiperidine; quinazolines | EC 3.4.14.5 (dipeptidyl-peptidase IV) inhibitor; hypoglycemic agent |
kyp 2047 | |||
bms 477118 | adamantanes; azabicycloalkane; monocarboxylic acid amide; nitrile; tertiary alcohol | EC 3.4.14.5 (dipeptidyl-peptidase IV) inhibitor; hypoglycemic agent | |
alogliptin | alogliptin : A piperidine that is 3-methyl-2,4-dioxo-3,4-dihydropyrimidine carrying additional 2-cyanobenzyl and 3-aminopiperidin-1-yl groups at positions 1 and 2 respectively (the R-enantiomer). Used in the form of its benzoate salt for treatment of type 2 diabetes. alogliptin: structure in first source | nitrile; piperidines; primary amino compound; pyrimidines | EC 3.4.14.5 (dipeptidyl-peptidase IV) inhibitor; hypoglycemic agent |
gosogliptin | amino acid amide | ||
anagliptin | anagliptin: anagliptin hydrochloride salt is the active compound | amino acid amide | |
mk-3102 | pyrrolopyrazole |