Target Name: MST1
NCBI ID: G4485
Review Report on MST1 Target / Biomarker Content of Review Report on MST1 Target / Biomarker
MST1
Other Name(s): hepatocyte growth factor-like protein homolog | macrophage stimulating 1 (hepatocyte growth factor-like) | HGFL_HUMAN | Hepatocyte growth factor-like protein alpha chain | DNF15S2 | NF15S2 | Macrophage stimulating 1, transcript variant 1 | Hepatocyte growth factor-like protein beta chain | D3F15S2 | Hepatocyte growth factor-like protein (isoform 1) | MST1 variant 1 | Hepatocyte growth factor-like protein | macrophage-stimulating protein | macrophage stimulating 1 | MSP | Macrophage stimulatory protein | Macrophage-stimulating protein | HGFL

Targeting MST1: A Potential Drug Target for Therapeutic Effects

MST1 (hepatocyte growth factor-like protein homolog) is a protein that is expressed in various tissues, including the liver, spleen, and pancreas. It is a member of the tyrosine kinase family, which includes proteins that play a crucial role in cell signaling . MST1 has been shown to be involved in several cellular processes, including cell growth, angiogenesis, and inflammation.

MST1 has also been identified as a potential drug target. Studies have shown that MST1 can be targeted by small molecules, such as inhibitors, which can inhibit the activity of the tyrosine kinase. These inhibitors have been shown to have therapeutic effects in a variety of diseases, including cancer, neurodegenerative diseases, and autoimmune disorders.

One of the challenges in targeting MST1 is its high expression level. MST1 is expressed in most tissues and has a strong expression in the liver, which makes it difficult to target it specifically. However, researchers have found that inhibitors can be used to reduce the expression of MST1 in specific tissues, such as the liver, and still have therapeutic effects.

Another challenge is the potential side effects of targeting MST1. MST1 is involved in many cellular processes, including cell growth, angiogenesis, and inflammation, which could make it difficult to predict the effects of targeting it. However, researchers have found that inhibitors can be used to specifically target the activity of MST1, rather than its whole cell, which should reduce the potential for side effects.

Targeting MST1 has been shown to have potential therapeutic effects in several diseases. For example, studies have shown that inhibitors of MST1 have been shown to have therapeutic effects in neurodegenerative diseases, such as Alzheimer's disease and Parkinson's disease. with inhibitors can reduce the symptoms of these diseases and improve the quality of life for patients.

In addition, MST1 has also been shown to be involved in cancer, and inhibitors of MST1 have been shown to have therapeutic effects in cancer treatment. These studies have shown that targeting MST1 with inhibitors can reduce the growth of cancer cells and improve the overall clinical outcome for cancer patients.

Overall, MST1 is a protein that has been shown to be involved in several cellular processes and has been identified as a potential drug target. While there are challenges in targeting MST1 specifically, researchers have found that inhibitors can be used to specifically target the activity of MST1 and have shown that these inhibitors have therapeutic effects in several diseases. Further research is needed to fully understand the potential of MST1 as a drug target and to develop safe and effective treatments.

Protein Name: Macrophage Stimulating 1

The "MST1 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 MST1 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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