Target Name: EMD
NCBI ID: G2010
Review Report on EMD Target / Biomarker Content of Review Report on EMD Target / Biomarker
EMD
Other Name(s): EDMD | Emerin | emerin | LEMD5 | STA | LEM domain containing 5 | EMD_HUMAN

EMD: A Potential Drug Target for Cancer

EMD (erythritol myeloid differentiation) is a protein that is expressed in the myeloid cells of the human body. It is a key regulator of hematopoietic stem cell (HSC) proliferation and has been shown to play a role in the development and progression of various diseases, including cancer. As a drug target, EMD has the potential to be used to treat a variety of conditions.

EMD is a transmembrane protein that is expressed in the cells of the bone marrow, where it plays a role in the development and maturation of hematopoietic stem cells (HSCs). HSCs are a type of stem cell that have the ability to develop into any type of blood cell in the body, including red blood cells, white blood cells, and platelets. EMD is believed to regulate the proliferation and differentiation of HSCs by controlling the activity of several key genes.

One of the functions of EMD is to regulate the self-renewal of HSCs. Self-renewal is the process by which a cell stays in a state of cell division and is able to maintain its own population of cells over time. EMD has been shown to play a key role in this process by regulating the activity of the stem cell factor (SCF) gene, which is a key regulator of self-renewal.

EMD has also been shown to regulate the differentiation of HSCs into different types of blood cells. This is important for the development of blood cells, as the cells of the immune system are responsible for protecting the body against infection and disease. EMD has been shown to play a key role in this process by regulating the activity of the myeloid differentiation antigen (MDA) gene, which is a key regulator of differentiation.

In addition to its role in regulating HSCs, EMD has also been shown to play a role in the development and progression of certain diseases. For example, EMD has been shown to be involved in the development of leukemia, a type of cancer that affects the bone marrow. Leukemia is characterized by the uncontrolled proliferation of white blood cells, which can lead to a wide range of symptoms and is a leading cause of cancer death. EMD has been shown to play a key role in the development of leukemia by regulating the activity of several key genes, including the BCR gene, which is a key regulator of leukemia development.

As a drug target, EMD has the potential to be used to treat a variety of conditions, including cancer. For example, EMD has been shown to be an effective inhibitor of the kinase activity of the Bcr gene, which is a key regulator of leukemia development. This suggests that EMD could be an effective treatment for leukemia by inhibiting the activity of the Bcr gene and reducing the proliferation of white blood cells.

In addition to its potential as a leukemia treatment, EMD has also been shown to have potential as a drug target for other conditions. For example, EMD has been shown to be an effective inhibitor of the angiogenesis of cancer cells, which is the process by which cancer cells grow and develop into tumors. This suggests that EMD could be an effective treatment for a variety of cancers by inhibiting the growth and development of cancer cells.

EMD is also being targeted as a potential biomarker for cancer. Its ability to regulate the proliferation and differentiation of HSCs makes it an attractive candidate for use as a biomarker for cancer. By measuring the levels of EMD in cancer cells, researchers can gain insight into the effectiveness of different treatments and the extent of cancer growth. This information could be used to improve the treatment of cancer and improve the overall health of patients.

In conclusion, EMD is a protein that is expressed in the myeloid cells of the human body and plays a key role in the development and regulation of hematopoietic stem cells. As a drug target, EMD has the potential to be used to treat a variety of conditions, including cancer. Its ability to regulate the proliferation and differentiation of HSCs makes it an attractive candidate for use as a

Protein Name: Emerin

Functions: Stabilizes and promotes the formation of a nuclear actin cortical network. Stimulates actin polymerization in vitro by binding and stabilizing the pointed end of growing filaments. Inhibits beta-catenin activity by preventing its accumulation in the nucleus. Acts by influencing the nuclear accumulation of beta-catenin through a CRM1-dependent export pathway. Links centrosomes to the nuclear envelope via a microtubule association. Required for proper localization of non-farnesylated prelamin-A/C. Together with NEMP1, contributes to nuclear envelope stiffness in germ cells (PubMed:32923640). EMD and BAF are cooperative cofactors of HIV-1 infection. Association of EMD with the viral DNA requires the presence of BAF and viral integrase. The association of viral DNA with chromatin requires the presence of BAF and EMD

The "EMD 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 EMD 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

EME1 | EME2 | EMG1 | EMID1 | EMILIN1 | EMILIN2 | EML1 | EML2 | EML2-AS1 | EML3 | EML4 | EML4-AS1 | EML5 | EML6 | EMP1 | EMP2 | EMP2P1 | EMP3 | EMSLR | EMSY | EMX1 | EMX2 | EMX2OS | EN1 | EN2 | ENAH | ENAM | ENC1 | ENDOD1 | ENDOG | Endogenous Retrovirus group K Env polyprotein (ERVK) | Endogenous retrovirus group K member 25 Pol protein-like, transcript variant X1 | EndoGlyx-1 | Endoplasmic reticulum collagen prolyl 3-hydroxylation complex | Endothelin receptor | Endothelin-Converting Enzymes (ECE) | Endothiapepsin | ENDOU | ENDOV | ENG | ENGASE | ENHO | ENKD1 | ENKUR | ENO1 | ENO1-AS1 | ENO1P1 | ENO1P4 | ENO2 | ENO3 | ENO4 | ENOPH1 | eNoSC Complex | ENOSF1 | ENOX1 | ENOX1-AS2 | ENOX2 | ENPEP | ENPP1 | ENPP2 | ENPP3 | ENPP4 | ENPP5 | ENPP6 | ENPP7 | ENPP7P10 | ENPP7P12 | ENPP7P7 | ENSA | ENSAP2 | ENTHD1 | ENTPD1 | ENTPD1-AS1 | ENTPD2 | ENTPD3 | ENTPD3-AS1 | ENTPD4 | ENTPD5 | ENTPD6 | ENTPD7 | ENTPD8 | ENTR1 | ENTREP1 | ENTREP2 | ENTREP3 | env | ENY2 | EOGT | EOLA1 | EOLA1-DT | EOLA2 | EOLA2-DT | EOMES | EP300 | EP300-AS1 | EP400 | EP400P1 | EPAS1 | EPB41 | EPB41L1