Target Name: TIMP3
NCBI ID: G7078
Review Report on TIMP3 Target / Biomarker Content of Review Report on TIMP3 Target / Biomarker
TIMP3
Other Name(s): SFD | Tissue inhibitor of metalloproteinases 3 | tissue inhibitor of metalloproteinases 3 | K222TA2 | K222 expressed in degenerative retinas | K222 | TIMP-3 | TIMP3_HUMAN | TIMP metallopeptidase inhibitor 3 | MIG-5 protein | Metalloproteinase inhibitor 3 | protein MIG-5 | HSMRK222 | Protein MIG-5

Introduction to TIMP3, A Potential Drug Target

In the field of medicine and pharmaceutical research, the identification of drug targets and biomarkers plays a crucial role in the development of new therapies and diagnostic tools. One such drug target that has gained significant attention is Tissue Inhibitor of Metalloproteinase 3 (TIMP3). TIMP3 is a protein that has demonstrated promising potential as a drug target and biomarker for various diseases. This article aims to provide an in-depth understanding of TIMP3, its role in disease progression, its significance as a drug target, and its potential as a biomarker.

The Role of TIMP3 in Disease Progression

TIMP3 is a member of the tissue inhibitor of metalloproteinases (TIMPs) family, which are known for their ability to inhibit the activity of matrix metalloproteinases (MMPs). MMPs are a group of enzymes responsible for the degradation of extracellular matrix components. Their dysregulation has been implicated in various pathological processes, including cancer, cardiovascular diseases, and neurodegenerative disorders.

In the context of cancer, for instance, TIMP3 has been shown to play a significant role in the inhibition of tumor growth and metastasis. Studies have revealed that TIMP3 can inhibit angiogenesis, the formation of new blood vessels that supply oxygen and nutrients to tumors. Additionally, TIMP3 can promote apoptosis, the programmed cell death of cancer cells, thereby preventing their uncontrolled growth and spread.

Moreover, TIMP3 has been implicated in various cardiovascular diseases, including arterial stenosis and atherosclerosis. It acts as a protector of the arterial wall integrity by inhibiting the degradation of extracellular matrix components and preventing the migration and proliferation of vascular smooth muscle cells. Dysregulation of TIMP3 in these conditions can contribute to the development and progression of arterial diseases.

TIMP3 as a Drug Target

The inhibition of TIMP3 has emerged as a potential therapeutic strategy for several diseases. By inhibiting TIMP3, the activity of MMPs can be unleashed, leading to enhanced extracellular matrix degradation. This is particularly relevant in the context of cancer, where MMPs are involved in tumor invasion and metastasis. Inhibiting TIMP3 can help to increase the activity of MMPs, resulting in the suppression of tumor growth and the prevention of metastatic spread.

Furthermore, the dysregulation of TIMP3 has been observed in diseases such as arthritis and age-related macular degeneration. In these conditions, the restoration or augmentation of TIMP3 levels can be a viable therapeutic approach. Various strategies have been investigated to target TIMP3, including the use of small molecule inhibitors and gene therapy approaches. Small molecule inhibitors that can selectively inhibit TIMP3 have shown promising results in preclinical studies, highlighting their potential as future therapeutic agents.

TIMP3 as a Biomarker

Apart from its potential as a drug target, TIMP3 has also garnered attention as a biomarker for disease diagnosis and prognosis. Biomarkers are measurable indicators that can provide valuable information about the presence, severity, or progression of a particular disease. TIMP3 has shown promise as a biomarker in several pathological conditions.

In cancer, for example, the expression levels of TIMP3 have been found to be altered in various types of tumors. High levels of TIMP3 have been associated with a better prognosis and increased patient survival in certain cancers, such as breast and ovarian cancer. Conversely, low levels of TIMP3 have been correlated with a poor prognosis and the aggressive behavior of tumors.

Additionally, the dysregulation of TIMP3 has been implicated in neurodegenerative disorders like Alzheimer's disease. Altered levels of TIMP3 have been detected in the brains of affected individuals, suggesting its involvement in the pathological processes underlying the disease. Monitoring TIMP3 levels in cerebrospinal fluid or blood samples could potentially aid in the early diagnosis and tracking of disease progression.

Conclusion

TIMP3 has emerged as a promising drug target and biomarker in various diseases. Its ability to inhibit MMPs makes it an attractive target for therapeutic intervention in conditions such as cancer and cardiovascular diseases. Furthermore, TIMP3's expression levels have shown significant correlations with the prognosis and aggressiveness of certain cancers, making it a potential biomarker for disease diagnosis and patient management.

Further research and development are needed to fully explore the therapeutic and diagnostic potentials of TIMP3. However, the current body of evidence suggests that TIMP3 holds great promise in improving the outcomes of patients with various diseases. It serves as a testament to the importance of molecular targets like TIMP3 in advancing the field of medicine and paving the way for personalized therapies and precision medicine.

Protein Name: TIMP Metallopeptidase Inhibitor 3

Functions: Complexes with metalloproteinases (such as collagenases) and irreversibly inactivates them by binding to their catalytic zinc cofactor. May form part of a tissue-specific acute response to remodeling stimuli. Known to act on MMP-1, MMP-2, MMP-3, MMP-7, MMP-9, MMP-13, MMP-14 and MMP-15

The "TIMP3 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about TIMP3 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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