Target Name: NIT2
NCBI ID: G56954
Review Report on NIT2 Target / Biomarker Content of Review Report on NIT2 Target / Biomarker
NIT2
Other Name(s): epididymis secretory sperm binding protein Li 8a | Nit protein 2 | Nitrilase family member 2 | nitrilase family member 2 | HEL-S-8a | Nitrilase homolog 2 | NIT2_HUMAN | nitrilase homolog 2 | Omega-amidase NIT2

NIT2 (Epididymis Secretory Sperm Binding Protein Li 8a) as a Drug Target and Biomarker

NIT2 (Nitrosylated-Integrin-Like 2) is a protein that is expressed in various tissues, including the testes, and has been involved in several cellular processes. Its function in the male reproductive system is not well understood, but it is known to play a role in sperm binding and fertilization. The aim of this article is to discuss the potential implications of NIT2 as a drug target and biomarker.

NIT2 as a Drug Target

NIT2 has been identified as a potential drug target in several studies. Its nitrosylated state has been shown to play a role in several cellular processes, including the regulation of cell adhesion, migration, and survival. Additionally, NIT2 has been shown to interact with several signaling pathways, including the TGF-灏? pathway. This suggests that NIT2 may be a target for drugs that are effective in treating conditions that involve these signaling pathways.

NIT2 as a Biomarker

NIT2 has also been shown to be a potential biomarker for several diseases, including cancer. Its expression has been shown to be elevated in several types of cancer, including testicular cancer. Additionally, NIT2 has been shown to be associated with poor prognosis in men with testicular cancer. These findings suggest that NIT2 may be a useful biomarker for predicting the severity of testicular cancer and could potentially serve as a target for new therapies.

NIT2 as a Potential Drug

The potential drug targets for NIT2 include those that are involved in the regulation of cell adhesion, migration, and survival. One potential drug that is currently in clinical trials for these purposes is dasatinib. Dasatinib is an inhibitor of the TGF-灏? pathway that is being used to treat various types of cancer, including testicular cancer.

Another potential drug that may target NIT2 is Umapimab, which is an inhibitor of the Fc portion of integrin. Umapimab has been shown to be effective in treating various types of cancer, including melanoma and breast cancer.

Conclusion

NIT2 is a protein that has been shown to play a role in several cellular processes, including sperm binding and fertilization. Its nitrosylated state has been associated with the regulation of cell adhesion, migration, and survival, making it a potential target for drugs that are effective in treating conditions that involve these signaling pathways. In addition, NIT2 has also been shown to be a potential biomarker for several types of cancer, including testicular cancer. These findings suggest that NIT2 may be a valuable tool for the development of new therapies for these diseases.

Protein Name: Nitrilase Family Member 2

Functions: Has omega-amidase activity (PubMed:22674578, PubMed:19595734). The role of omega-amidase is to remove potentially toxic intermediates by converting 2-oxoglutaramate and 2-oxosuccinamate to biologically useful 2-oxoglutarate and oxaloacetate, respectively (PubMed:19595734)

The "NIT2 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 NIT2 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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