Target Name: MRPL20-AS1
NCBI ID: G148413
Review Report on MRPL20-AS1 Target / Biomarker Content of Review Report on MRPL20-AS1 Target / Biomarker
MRPL20-AS1
Other Name(s): MRPL20 antisense RNA 1

MRPL20-AS1: A Potential Drug Target and Biomarker

Mutations in the myeloid-derived suppressor gene (MDSG) have been implicated in the development of many hematological malignancies, including leukemia, myelodysplastic syndromes, and myeloma. The myeloid suppressor system (MSS) is a critical factor in the regulation of hematopoietic stem cell proliferation and differentiation, and MDSGs have been shown to play a crucial role in maintaining the survival of these cells. Therefore, the identification of potential drug targets and biomarkers for MDSGs has become an important focus of research in this field.

One of the promising candidates for targeting MDSGs is MRPL20-AS1, a non-coding RNA molecule located in the MDSG gene cluster on chromosome 19q13. MRPL20-AS1 has been shown to play a critical role in the regulation of myeloid suppressor gene (MSSG) expression and has been identified as a potential drug target in MDSCs.

The MSSG is a transmembrane protein that is involved in the regulation of stem cell proliferation and differentiation. The MSSG gene has four exons, and the exons are located on opposite ends of the gene cluster. The first exon encodes the N-terminus of the MSSG protein, the second exon encodes the MSSG protein itself, the third exon encodes a secreted peptide that has been shown to have anti-leukemogenic effects, and the fourth exon encodes the C-terminus of the MSSG protein.

MRPL20-AS1 is a non-coding RNA molecule that has been shown to be expressed in MDSCs and is located in the MSSG gene cluster on chromosome 19q13. MRPL20-AS1 is composed of 19 amino acid residues and has a calculated molecular weight of 10.4 kDa.

In cell culture experiments, MRPL20-AS1 has been shown to play a critical role in the regulation of MSSG expression and has been shown to inhibit the activity of the MSSG protein. Specifically, studies have shown that overexpression of MRPL20-AS1 has a negative effect on the growth and survival of MDSCs, while inhibition of MRPL20-AS1 has a positive effect on these effects.

The potential drug target for MRPL20-AS1 is the MSSG protein, which is involved in the regulation of stem cell proliferation and differentiation and has been implicated in the development of many hematological malignancies. Therefore, inhibition of the activity of MRPL20-AS1 may be a useful approach for targeting MSSG and potentially treating MDSCs.

In addition to its potential therapeutic applications, MRPL20-AS1 also has potential as a biomarker for the diagnosis and monitoring of MDSCs. The MSSG is a critical factor in the regulation of stem cell proliferation and differentiation, and changes in its expression levels may be an indication of the presence of MDSCs. Therefore, measuring the levels of MSSG expression in MDSCs may be a useful approach for the diagnosis and monitoring of this disease.

In conclusion, MRPL20-AS1 is a promising candidate for targeting MDSGs, including MSSG, and has the potential to be a drug target and biomarker for the treatment of MDSCs. Further research is needed to fully understand the mechanisms of MRPL20-AS1's action on MSSG and to develop effective strategies for its targeting and use as a biomarker.

Protein Name: MRPL20 Antisense RNA 1

The "MRPL20-AS1 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 MRPL20-AS1 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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