Target Name: STAM-DT
NCBI ID: G102723166
Review Report on STAM-DT Target / Biomarker Content of Review Report on STAM-DT Target / Biomarker
STAM-DT
Other Name(s): STAM divergent transcript | STAM-AS1 | locus3182

STAM-DT: A Potential Drug Target and Biomarker for STAM-Driven Transcriptional regulated Assays

Stimulated in part by the Human Genome Project, the transcriptional regulated assays (TRAs) have revolutionized our understanding of gene function and played a pivotal role in the identification of genetic mutations associated with various diseases. One of the key processes underlying these assays is the STAM (stimulated amino acid mutagenesis) system, which has been extensively studied in the context of cancer and neurodegenerative diseases. In this article, we will explore the concept of STAM-DT, or STAM-driven transcriptional regulated assays, as a potential drug target and biomarker for human disease.

The Basics of STAM-DT

STAM-DT is a type of stimulated amino acid mutagenesis (SAMM) system that was first described by Avida and colleagues in 2008. In this system, a single amino acid is mutated in a plasmid-mediated manner, which is then introduced into the cell to be transcribed into RNA. This RNA can then be used for a variety of downstream analyses, including transcriptional regulation assays.

One of the key features of STAM-DT is its ability to specifically target and regulate gene expression in a tissue or cell-specific manner. This is achieved by the use of a specific plasmid, which contains a regulatory region that is only active when the mutated amino acid is present in the cell. This allows for highly specific and targeted regulation of gene expression, which is particularly useful for the study of complex cellular processes.

Applications of STAM-DT in the Context of Disease

The applications of STAM-DT in disease research are vast and varied. In cancer, STAM-DT has been used to study the regulation of gene expression associated with various oncogenic processes, including cell division, angiogenesis, and drug resistance. For example, studies have shown that STAM-DT can be used to effectively knockdown the expression of genes involved in cell division and apoptosis, leading to a reduction in cancer cell proliferation.

In neurodegenerative diseases, STAM-DT has been used to investigate the regulation of gene expression in the context of neurodegeneration. For example, studies have shown that STAM-DT can be used to effectively knockdown the expression of genes involved in neurotransmitter synthesis and release, leading to a reduction in neurodegeneration.

Potential Therapeutic Benefits

The potential therapeutic benefits of STAM-DT are numerous and varied. In cancer, STAM-DT has the potential to be used as a targeted therapy by introducing small, specific mutations into cancer cells. This can lead to a reduction in cell proliferation and a decrease in the overall risk of cancer recurrence.

In neurodegenerative diseases, STAM-DT has the potential to be used as a therapeutic approach by introducing mutations into the genes involved in neurodegeneration. This can lead to a reduction in neurodegeneration and improve overall quality of life for individuals with these conditions.

Conclusion

In conclusion, STAM-DT is a promising technology that has the potential to revolutionize our understanding of gene function and the study of disease. Its ability to specifically target and regulate gene expression in a tissue or cell-specific manner makes it an attractive tool for a variety of cellular and downstream biological studies. Further research is needed to fully explore the potential therapeutic benefits of STAM-DT and to develop it as a useful tool for the study of human disease.

Protein Name: STAM Divergent Transcript

The "STAM-DT 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 STAM-DT 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

More Common Targets

STAM2 | STAMBP | STAMBPL1 | STAP1 | STAP2 | STAR | STARD10 | STARD13 | STARD3 | STARD3NL | STARD4 | STARD4-AS1 | STARD5 | STARD6 | STARD7 | STARD7-AS1 | STARD8 | STARD9 | STARP1 | STAT1 | STAT2 | STAT3 | STAT4 | STAT4-AS1 | STAT5 | STAT5A | STAT5B | STAT6 | STATH | STAU1 | STAU2 | STAU2-AS1 | STBD1 | STC1 | STC2 | STEAP1 | STEAP1B | STEAP2 | STEAP2-AS1 | STEAP3 | STEAP3-AS1 | STEAP4 | STEEP1 | Steroid 5-alpha-Reductase | Sterol O-acyltransferase (ACAT) | Sterol Regulatory Element-Binding Protein | STH | STIL | STIM1 | STIM2 | STIMATE | STIN2-VNTR | STING1 | STIP1 | STK10 | STK11 | STK11IP | STK16 | STK17A | STK17B | STK19 | STK24 | STK25 | STK26 | STK3 | STK31 | STK32A | STK32A-AS1 | STK32B | STK32C | STK33 | STK35 | STK36 | STK38 | STK38L | STK39 | STK4 | STK4-DT | STK40 | STKLD1 | STMN1 | STMN2 | STMN3 | STMN4 | STMND1 | STMP1 | STN1 | STOM | STOML1 | STOML2 | STOML3 | STON1 | STON1-GTF2A1L | STON2 | Store-operating calcium channel channels | STOX1 | STOX2 | STPG1 | STPG2 | STPG3