Target Name: TGFBI
NCBI ID: G7045
Review Report on TGFBI Target / Biomarker Content of Review Report on TGFBI Target / Biomarker
TGFBI
Other Name(s): CSD3 | Beta IG-H3 | CDGG1 | CSD | betaig-h3 | CSD1 | beta ig-h3 | BGH3_HUMAN | Kerato-epithelin | RGD-CAP | CDB1 | CDG2 | transforming growth factor beta induced | RGD-containing collagen-associated protein | BIGH3 | transforming growth factor beta-induced 68kDa | LCD1 | CSD2 | transforming growth factor, beta-induced, 68kD | kerato-epithelin | RGD-containing collagen associated protein | Transforming growth factor beta induced | Transforming growth factor-beta-induced protein ig-h3 | Beta ig-h3 | EBMD

TGFBI as a Potential Drug Target in Disease Treatment

Introduction:

In recent years, there has been a growing interest in identifying novel drug targets or biomarkers that play crucial roles in the development and progression of various diseases. One such target is Transforming Growth Factor Beta-Induced protein (TGFBI), which has gained significant attention due to its involvement in several pathological processes. This article aims to delve into the intricacies of TGFBI and discuss its potential as a drug target or biomarker in disease treatment.

The Role of TGFBI in Disease:

TGFBI, a glycoprotein, is primarily known for its involvement in the progression of fibrosis, inflammation, and cancer. Preclinical studies have demonstrated that TGFBI expression is significantly upregulated in various pathological conditions, including liver fibrosis, cardiac fibrosis, pulmonary fibrosis, and renal fibrosis. These findings suggest that TGFBI may serve as a potential drug target with the aim of inhibiting fibrotic processes and reducing associated complications.

Moreover, TGFBI has been implicated in promoting chronic inflammation, which plays a vital role in the development and progression of numerous diseases. In inflammatory bowel disease, for instance, TGFBI expression is upregulated in the inflamed intestinal mucosa, and its presence correlates with disease severity. In addition, TGFBI has been shown to modulate immune responses and enhance tissue damage, thereby further reinforcing its potential as a therapeutic target in inflammatory diseases.

Another crucial aspect of TGFBI's role in disease development is its association with cancer. Studies have reported that TGFBI expression is upregulated in various types of cancer, including breast, lung, colorectal, and pancreatic cancer. TGFBI promotes tumor growth and metastasis by enhancing angiogenesis, the process of forming new blood vessels, and by modulating extracellular matrix remodeling, facilitating cancer cell invasion. Targeting TGFBI could thus offer new opportunities in combating cancer progression and improving patient outcomes.

Targeting TGFBI in Therapeutic Strategies:

The unique properties and pivotal role of TGFBI in various diseases make it an attractive target for therapeutic interventions. Several approaches have been explored in targeting TGFBI effectively, including small-molecule inhibitors, monoclonal antibodies, and RNA-based therapies.

Small-molecule inhibitors of TGFBI aim to block its interactions with specific receptors or downstream signaling molecules. These inhibitors have shown promising results in preclinical studies, attenuating fibrotic processes, inhibiting chronic inflammation, and suppressing tumor growth. However, further research is required to enhance specificity and efficacy before these inhibitors can be translated into clinical use.

Monoclonal antibodies, on the other hand, offer a more targeted approach to neutralizing TGFBI. By specifically recognizing and binding to TGFBI, monoclonal antibodies can exert their therapeutic effects, including reduced fibrosis, suppressed inflammation, and inhibited tumor growth. Several clinical trials are currently investigating the safety and efficacy of monoclonal antibodies targeting TGFBI in patients with fibrosis or cancer, providing hope for future therapeutic options.

Additionally, RNA-based therapies have emerged as a promising approach to modulating TGFBI expression. Techniques such as RNA interference and antisense oligonucleotides can effectively silence TGFBI expression, preventing its detrimental effects. These techniques have shown success in preclinical studies and hold great potential as future treatment modalities.

TGFBI as a Potential Biomarker:

Besides its potential as a drug target, TGFBI also demonstrates promise as a biomarker for disease diagnosis, prognosis, and monitoring. The upregulation of TGFBI has been correlated with disease severity and progression in several conditions, including fibrosis and cancer. Identifying increased levels of TGFBI in biological samples, such as blood or tissue, could aid in early disease detection, assessing disease aggressiveness, and monitoring treatment response.

Conclusion:

Transforming Growth Factor Beta-Induced protein (TGFBI) has emerged as a compelling drug target and biomarker in disease treatment. Its involvement in fibrosis, chronic inflammation, and cancer has sparked significant interest among researchers and pharmaceutical companies to develop therapies aimed at blocking or modulating its function. Continued research and clinical trials are essential to fully explore the potential of TGFBI and harness its therapeutic benefits, paving the way for improved treatment strategies and better patient outcomes.

Protein Name: Transforming Growth Factor Beta Induced

Functions: Plays a role in cell adhesion (PubMed:8024701). May play a role in cell-collagen interactions (By similarity)

The "TGFBI 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 TGFBI 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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