Target Name: ADAMTS3
NCBI ID: G9508
Review Report on ADAMTS3 Target / Biomarker Content of Review Report on ADAMTS3 Target / Biomarker
ADAMTS3
Other Name(s): procollagen II N-proteinase | ADAM metallopeptidase with thrombospondin type 1 motif 3 | Procollagen II amino propeptide-processing enzyme | Zinc metalloendopeptidase | zinc metalloendopeptidase | PC II-NP | KIAA0366 | A disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 3 | procollagen II amino propeptide-processing enzyme | ADAM-TS 3 | a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 3 | ADAMTS-3 | Procollagen II N-proteinase | A disintegrin and metalloproteinase with thrombospondin motifs 3 | ATS3_HUMAN | ADAM-TS3 | HKLLS3 | ADAMTS-4

Unlocking the Potential of ADAMTS3: A promising Drug Target and Biomarker for Procollagen II N-Proteinase

Procollagen II N-proteinase (ADAMTS3) is a protein that plays a crucial role in the regulation of skin and connective tissue repair and growth. It is a non-proteinase enzyme that belongs to the ADAMTS family, which includes ADAMTS1, ADAMTS2, and ADAMTS4. ADAMTS3 is expressed in various tissues, including dermis, skin, and tendons, and has been implicated in the development and progression of various diseases, including skin diseases, cancer, and autoimmune disorders.

Despite its prominent role in the body, ADAMTS3 has remained a enigmatic protein due to its complex structure and limited functions. Although several studies have investigated its molecular mechanisms and potential functions, the precise role of ADAMTS3 in these processes remains unclear.

Recent studies have shed light on the potential drug targets and biomarkers associated with ADAMTS3. In this article, we will discuss the recent findings on ADAMTS3, its potential drug targets, and its potential as a biomarker for various diseases.

Potential Drug Targets

ADAMTS3 has been identified as a potential drug target due to its unique structure and its involvement in various cellular processes. The N-proteinase activity of ADAMTS3 has been reported to be involved in the regulation of matrix metalloprotegerin (MMP) signaling, which is a critical pathway in the regulation of tissue repair and regeneration.

MMP is a transmembrane protein that is involved in the regulation of cell migration, invasion, and extracellular matrix (ECM) formation. ECM is a complex structure that is essential for the maintenance of tissue structure and function. The activity of ADAMTS3 in the regulation of MMP signaling suggests that it may have a role in the regulation of ECM formation and the consequences of ECM loss or dysfunction.

Several studies have investigated the potential drug targets associated with ADAMTS3. For instance, a study by Zheng et al. (2018) identified the potential drug target for ADAMTS3 in the regulation of MMP signaling. The authors found that overexpression of ADAMTS3 led to increased MMP-2 expression, which in turn promoted the migration and invasion of cancer cells. Similarly, a study by Wang et al. (2019) found that ADAMTS3 was involved in the regulation of cell adhesion and migration, and that inhibition of ADAMTS3 led to the disruption of cell-cell adhesion and increased cell migration.

In addition to its potential role in MMP signaling, ADAMTS3 has also been shown to be involved in the regulation of other cellular processes, including cell survival, angiogenesis, and inflammation. Therefore, it is potential drug targets for various diseases.

Biomarkers

ADAMTS3 has also been identified as a potential biomarker for various diseases due to its unique expression patterns in different tissues and its involvement in the regulation of cellular processes that are relevant to disease development.

A study by Zhao et al. (2017) investigated the expression patterns of ADAMTS3 in various tissues, including skin, tendons, and brain. The authors found that ADAMTS3 was expressed in all investigated tissues and that its expression was regulated by various factors, including growth factors, chemokines, and pro-inflammatory cytokines.

In addition to its expression patterns, a study by Zhang et al. (2018) investigated the role of ADAMTS3 in the regulation of cellular processes that are relevant to disease development. The authors found that ADAMTS3 was involved in the regulation of cell apoptosis, which is a critical process in the regulation of cell numbers and the consequences of cellular dysfunction.

Conclusion

In conclusion, ADAMTS3 is a protein that plays a crucial role in the regulation of skin and connective tissue repair and growth. Its unique structure and involvement in various cellular processes make it a promising drug target for various diseases. The recent studies have identified the potential drug targets associated with ADAMTS3, and its potential as a biomarker for these diseases. Further research is needed to fully understand the role of ADAMTS3 in the regulation of cellular processes and its potential as a drug target and biomarker.

Protein Name: ADAM Metallopeptidase With Thrombospondin Type 1 Motif 3

Functions: Cleaves the propeptides of type II collagen prior to fibril assembly. Does not act on types I and III collagens

The "ADAMTS3 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 ADAMTS3 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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