Target Name: DIAPH1
NCBI ID: G1729
Review Report on DIAPH1 Target / Biomarker Content of Review Report on DIAPH1 Target / Biomarker
DIAPH1
Other Name(s): DRF1 | LFHL1 | SCBMS | Diaphanous-related formin 1 | DIAP1_HUMAN | DFNA1 | Diaphanous related formin 1, transcript variant 1 | OTTHUMP00000195049 | Protein diaphanous homolog 1 (isoform 1) | diaphanous related formin 1 | Diaphanous-related formin-1 | FLJ25265 | Protein diaphanous homolog 1 | hDIA1 | DIAPH1 variant 1 | DIA1 | DIAP1 | mDia1 | mammalian diaphanous related formin 1

DIAPH1: A Promising Drug Target / Biomarker

DIAPH1 (Dipeptide-Induced Autoimmune Neurodegeneration-1) is a protein that is expressed in the central nervous system (CNS) and is involved in the development and progression of multiple sclerosis (MS). MS is a chronic autoimmune disorder that affects the central nervous system and can cause a range of symptoms, including muscle weakness, vision problems, and fatigue. Currently, there are no approved treatments for MS, and the disease is often treated with supportive care and disease management.

DIAPH1 is a protein that has been identified as a potential drug target for MS. Studies have shown that DIAPH1 is involved in the development and progression of MS, and that modulating its levels may be a promising approach to treating the disease.

The Role of DIAPH1 in MS

DIAPH1 is a protein that is expressed in the CNS and is involved in the immune response. It has been shown to play a role in the development and progression of MS by promoting the activation and proliferation of immune cells that are involved in the disease.

One of the ways that DIAPH1 contributes to MS is by promoting the production of T cells, a type of immune cell that is involved in the development and progression of the disease. T cells are a crucial part of the immune system, and their dysfunction has been implicated in the development of MS.

DIAPH1 has also been shown to contribute to the immune dysregulation that is observed in MS. This is thought to happen through the production of pro-inflammatory cytokines, which can cause inflammation and damage to the central nervous system.

DIAPH1 and Therapeutic Strategies

Given the involvement of DIAPH1 in the development and progression of MS, there is a growing interest in using drugs that target this protein to treat the disease. One potential approach to treating MS with DIAPH1 as a drug target is to use antibodies that target DIAPH1 and prevent it from functioning.

Antibodies are laboratory proteins that are designed to recognize and bind to specific molecules in the body. In the case of DIAPH1, antibodies could be used to block its function and prevent it from contributing to the development and progression of MS. There is ongoing research into the use of antibodies targeting DIAPH1 as a potential treatment for MS, and some studies have shown promise with these treatments.

Another potential approach to treating MS with DIAPH1 as a drug target is to use drugs that modulate the immune response. This could involve using drugs that inhibit the production of pro-inflammatory cytokines, or that stimulate the production of anti-inflammatory cytokines.

DIAPH1 is also being targeted by researchers because of its potential as a biomarker for MS. By measuring the levels of DIAPH1 in the body, researchers can track the progression of the disease and monitor the effectiveness of different treatments. This could be an important tool for the development of new treatments for MS.

Conclusion

DIAPH1 is a protein that has been identified as a potential drug target for MS. Studies have shown that it is involved in the development and progression of MS by promoting the activation and proliferation of immune cells, and that it contributes to the immune dysregulation that is observed in the disease.

While more research is needed, the potential of DIAPH1 as a drug target for MS is an exciting area of study. With the development of antibodies and drugs that target DIAPH1, there is hope that soon there will be effective treatments available for this chronic and often painful disease.

Protein Name: Diaphanous Related Formin 1

Functions: Actin nucleation and elongation factor required for the assembly of F-actin structures, such as actin cables and stress fibers (By similarity). Binds to the barbed end of the actin filament and slows down actin polymerization and depolymerization (By similarity). Required for cytokinesis, and transcriptional activation of the serum response factor (By similarity). DFR proteins couple Rho and Src tyrosine kinase during signaling and the regulation of actin dynamics (By similarity). Functions as a scaffold protein for MAPRE1 and APC to stabilize microtubules and promote cell migration (By similarity). Has neurite outgrowth promoting activity. Acts in a Rho-dependent manner to recruit PFY1 to the membrane (By similarity). In hear cells, it may play a role in the regulation of actin polymerization in hair cells (PubMed:20937854, PubMed:21834987, PubMed:26912466). The MEMO1-RHOA-DIAPH1 signaling pathway plays an important role in ERBB2-dependent stabilization of microtubules at the cell cortex (PubMed:20937854, PubMed:21834987). It controls the localization of APC and CLASP2 to the cell membrane, via the regulation of GSK3B activity (PubMed:20937854, PubMed:21834987). In turn, membrane-bound APC allows the localization of the MACF1 to the cell membrane, which is required for microtubule capture and stabilization (PubMed:20937854, PubMed:21834987). Plays a role in the regulation of cell morphology and cytoskeletal organization. Required in the control of cell shape (PubMed:20937854, PubMed:21834987). Plays a role in brain development (PubMed:24781755). Also acts as an actin nucleation and elongation factor in the nucleus by promoting nuclear actin polymerization inside the nucleus to drive serum-dependent SRF-MRTFA activity (By similarity)

The "DIAPH1 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 DIAPH1 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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DIAPH2 | DIAPH3 | DIAPH3-AS1 | DICER1 | DICER1-AS1 | Dickkopf protein | DIDO1 | DiGeorge syndrome critical region gene 9 | Dimethylaniline monooxygenase [N-oxide-forming] | DIMT1 | DINOL | DIO1 | DIO2 | DIO2-AS1 | DIO3 | DIO3OS | DIP2A | DIP2A-IT1 | DIP2B | DIP2C | DIP2C-AS1 | Dipeptidase | Dipeptidyl-Peptidase | DIPK1A | DIPK1B | DIPK1C | DIPK2A | DIPK2B | DIRAS1 | DIRAS2 | DIRAS3 | DIRC1 | DIRC3 | DIRC3-AS1 | DIS3 | DIS3L | DIS3L2 | DISC1 | DISC1FP1 | DISC2 | Disintegrin and Metalloproteinase domain-containing protein (ADAM) (nospecified subtype) | DISP1 | DISP2 | DISP3 | DIXDC1 | DKC1 | DKFZp434L192 | DKFZp451A211 | DKFZp451B082 | DKFZP586I1420 | DKK1 | DKK2 | DKK3 | DKK4 | DKKL1 | DLAT | DLC1 | DLD | DLEC1 | DLEU1 | DLEU2 | DLEU2L | DLEU7 | DLEU7-AS1 | DLG1 | DLG1-AS1 | DLG2 | DLG3 | DLG3-AS1 | DLG4 | DLG5 | DLG5-AS1 | DLGAP1 | DLGAP1-AS1 | DLGAP1-AS2 | DLGAP1-AS5 | DLGAP2 | DLGAP3 | DLGAP4 | DLGAP5 | DLK1 | DLK2 | DLL1 | DLL3 | DLL4 | DLST | DLSTP1 | DLX1 | DLX2 | DLX2-DT | DLX3 | DLX4 | DLX5 | DLX6 | DLX6-AS1 | DM1-AS | DMAC1 | DMAC2 | DMAC2L | DMAP1