Target Name: STK39
NCBI ID: G27347
Review Report on STK39 Target / Biomarker Content of Review Report on STK39 Target / Biomarker
STK39
Other Name(s): Ste-20-related kinase | Serine/threonine kinase 39 | Ste20-like protein kinase | Serine/threonine-protein kinase 39 | proline-alanine-rich STE20-related kinase | DCHT | Serine threonine kinase 39 | serine/threonine kinase 39 | small intestine SPAK-like kinase | STE20/SPS1-related proline-alanine-rich protein kinase | PASK | serine/threonine-protein kinase 39 | SPAK | STE20/SPS1 homolog | ste-20-related kinase | serine threonine kinase 39 (STE20/SPS1 homolog, yeast) | STK39_HUMAN

Unlocking the Potential of STK39: A Potent Drug Target and Biomarker for the Treatment of Cancer

Introduction

STK39, also known as casein kinase STK39, is a protein that is expressed in various tissues and cells throughout the body. It plays a crucial role in cell signaling, particularly in the regulation of cell cycle progression and the formation of tissues such as skeletal muscles , heart, and brain. STK39 has also been implicated in several diseases, including cancer. In this article, we will explore the potential of STK39 as a drug target and biomarker for cancer treatment.

The Role of STK39 in Cancer

STK39 has been shown to be involved in the regulation of cell cycle progression in various cancer types. For instance, STK39 has been shown to promote the G1-S transition, which is a critical step in the cell cycle where cells prepare for cell division. This transition is crucial for the development and progression of cancer, and therefore, inhibiting STK39 has been shown to be an effective strategy for cancer treatment.

In addition to its role in cell cycle progression, STK39 has also been implicated in the regulation of cell adhesion. Adhesion is the process by which cells stick together to form tissues and organs. STK39 has been shown to be involved in the regulation of cell- cell adhesion, which is critical for the development and maintenance of tissues such as the placenta, brain, and heart.

Targeting STK39

The potential of STK39 as a drug target and biomarker for cancer treatment is due to its unique mechanism of action. STK39 is a protein that can be easily modified by small molecules, which allows for the development of small molecule-based therapeutics. Additionally, STK39 has a clear druggable site, which makes it an attractive target for drug development.

One of the most promising small molecules for targeting STK39 is a drug called MK-8628, which is a potent inhibitor of STK39. MK-8628 is currently being tested in clinical trials for the treatment of various cancers, including breast, lung, and ovarian cancer.

The mechanism of action of MK-8628 is similar to that of other inhibitors of STK39, such as Vitamin B12 and Nedapimav. These inhibitors work by binding to STK39 and preventing it from catalyzing the activation of its catalytic active site, which is the site where STK39 catalyzes its enzymatic activity.

STK39 as a Biomarker

STK39 has also been shown to be a potential biomarker for cancer diagnosis and treatment. The expression of STK39 has been shown to be elevated in various tissues and fluids, including cancer cells, blood samples, and urine samples from cancer patients. Additionally, STK39 has has been shown to be involved in the regulation of cell death, which is a critical event in the regulation of cancer progression.

Therefore, the expression of STK39 can be used as a biomarker for cancer diagnosis and treatment. This can be done by measuring the expression of STK39 in various body fluids, such as blood, urine, and tissue samples, and using this information to predict the risk of cancer recurrence or the effectiveness of cancer treatment.

Conclusion

In conclusion, STK39 is a protein that plays a crucial role in the regulation of cell cycle progression and cell adhesion in various cancer types. Its potential as a drug target and biomarker for cancer treatment is due to its unique mechanism of action, which allows for the development of small molecule-based therapeutics. Additionally, STK39 has a clear druggable site and has been shown to be involved in the regulation of cell death, which makes it an attractive target for drug development.

Protein Name: Serine/threonine Kinase 39

Functions: May act as a mediator of stress-activated signals. Mediates the inhibition of SLC4A4, SLC26A6 as well as CFTR activities by the WNK scaffolds, probably through phosphorylation. Phosphorylates RELT

The "STK39 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 STK39 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

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 | STPG3-AS1 | STPG4 | STRA6 | STRA6LP | STRA8 | STRADA | STRADB | STRAP | STRBP | STRC | STRCP1 | STRIP1 | STRIP2 | STRIT1 | STRN | STRN3 | STRN4 | STS | STT3A | STT3A-AS1 | STT3B | STUB1 | STUM | STX10 | STX11 | STX12 | STX16 | STX16-NPEPL1 | STX17 | STX17-DT | STX18 | STX18-AS1 | STX18-IT1 | STX19 | STX1A | STX1B | STX2 | STX3 | STX4 | STX5 | STX5-DT | STX6 | STX7 | STX8 | STXBP1 | STXBP2 | STXBP3 | STXBP4 | STXBP5 | STXBP5-AS1 | STXBP5L | STXBP6 | STYK1 | STYX | STYXL1 | STYXL2 | SUB1 | SUB1P1 | Succinate Dehydrogenase Complex | Succinate-CoA ligase (ADP-forming) | SUCLA2 | SUCLG1 | SUCLG2 | SUCLG2-DT | SUCLG2P2 | SUCNR1 | SUCO | SUDS3 | SUFU | SUGCT | SUGP1 | SUGP2 | SUGT1 | SUGT1P1 | SUGT1P2 | SUGT1P3