Target Name: TIMP4
NCBI ID: G7079
Review Report on TIMP4 Target / Biomarker Content of Review Report on TIMP4 Target / Biomarker
TIMP4
Other Name(s): tissue inhibitor of metalloproteinase 4 | TIMP-4 | tissue inhibitor of metalloproteinases 4 | Tissue inhibitor of metalloproteinases 4 | Metalloproteinase inhibitor 4 | TIMP metallopeptidase inhibitor 4 | TIMP4_HUMAN | Tissue inhibitor of metalloproteinase 4

TIMP4: A Promising Drug Target in Disease Intervention

In the ever-evolving world of biomedical research, scientists constantly search for new drug targets and biomarkers to improve disease intervention and patient outcomes. Tissue inhibitor of metalloproteinase 4 (TIMP4) has emerged as a promising candidate in this regard. With its crucial role in regulating extracellular matrix (ECM) remodeling, TIMP4 presents an attractive avenue for therapeutic intervention. This article delves into the significance of TIMP4 as a potential drug target and biomarker, shedding light on its functions and implications in various diseases.

Understanding TIMP4

TIMP4 is a member of the TIMP family, which consists of four naturally occurring inhibitors of matrix metalloproteinases (MMPs). MMPs play an essential role in ECM remodeling and tissue homeostasis. They mediate the breakdown of ECM components such as collagen and elastin, contributing to various physiological and pathological processes. However, uncontrolled or dysregulated MMP activity can lead to tissue damage and contribute to the progression of diseases such as cancer, cardiovascular disorders, and fibrosis.

As an inhibitor of MMP activity, TIMP4 acts as a key regulator of ECM remodeling. By binding to MMPs, TIMP4 prevents their proteolytic activity, thereby preserving the integrity of the ECM. This delicate balance is crucial for maintaining tissue structure, function, and repair. Dysregulation of TIMP4 expression or altered TIMP4-MMP interactions can result in excessive ECM degradation or accumulation, leading to pathological conditions.

Roles of TIMP4 in Disease

Cancer
In the context of cancer, TIMP4 has been identified as a potential tumor suppressor. Studies have shown reduced expression of TIMP4 in various cancer types, including breast, lung, and prostate cancer. This downregulation is often associated with increased invasiveness, metastasis, and poor prognosis. The decreased levels of TIMP4 allow for uncontrolled MMP activity, facilitating tumor cell migration and invasion.

Cardiovascular Diseases
TIMP4 has also garnered attention in cardiovascular research due to its implications in heart failure, atherosclerosis, and cardiac remodeling. In heart failure, TIMP4 expression is often upregulated in the myocardium, suggesting a compensatory response to the detrimental effects of MMP-mediated tissue damage. However, excessive TIMP4 levels can disrupt the delicate balance between MMPs and TIMPs, leading to impaired ECM remodeling and fibrotic processes.

Similarly, TIMP4 has been implicated in atherosclerosis, an inflammatory condition characterized by the accumulation of cholesterol-rich plaques in arterial walls. Inflammatory cytokines and growth factors induce TIMP4 expression in atherosclerotic lesions, contributing to the stabilization of vulnerable plaques.

Fibrosis
Fibrosis, the excessive deposition of ECM components, is a common feature of many chronic diseases, including liver cirrhosis, pulmonary fibrosis, and renal fibrosis. TIMP4 has emerged as a potential therapeutic target to prevent or reverse fibrotic processes. Studies indicate that TIMP4 expression is dysregulated in fibrotic tissues, and its restoration or manipulation holds promise for reducing ECM accumulation and promoting tissue repair.

TIMP4 as a Drug Target

The emerging understanding of TIMP4's role in various diseases has sparked interest in developing therapeutics targeting this molecule. Several strategies are being explored, with the ultimate goal of modulating TIMP4 expression or function, and thereby restoring ECM homeostasis.

One approach involves gene therapy, where viral vectors or nanoparticles carrying TIMP4 genes are introduced into targeted tissues. By delivering TIMP4 directly to affected areas, researchers aim to rectify TIMP4 deficiencies and rebalance ECM remodeling.

Another strategy focuses on the development of small-molecule inhibitors that can selectively modulate TIMP4 activity. By designing compounds that mimic the inhibitory function of TIMP4, scientists aim to regulate MMP activity and restore ECM integrity.

TIMP4 as a Biomarker

Beyond its potential as a therapeutic target, TIMP4 also holds promise as a biomarker for disease diagnosis, prognosis, and treatment response. The altered expression of TIMP4 in various pathological conditions suggests its potential as an indicator of disease progression and severity. Biomarkers such as TIMP4 can aid in early detection, risk stratification, and monitoring of treatment efficacy.

Conclusion

TIMP4, with its pivotal role in ECM remodeling and disease progression, presents an exciting avenue for therapeutic intervention and biomarker development. Understanding the complex interactions between TIMP4 and MMPs opens the door to targeted therapies for cancer, cardiovascular diseases, and fibrosis. Further investigations are necessary to unravel the full potential of TIMP4, but the current body of knowledge suggests it as a promising drug target and biomarker for improved disease intervention and patient care.

Protein Name: TIMP Metallopeptidase Inhibitor 4

Functions: Complexes with metalloproteinases (such as collagenases) and irreversibly inactivates them by binding to their catalytic zinc cofactor. Known to act on MMP-1, MMP-2, MMP-3, MMP-7 and MMP-9

The "TIMP4 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 TIMP4 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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