Target Name: TBCE
NCBI ID: G6905
Review Report on TBCE Target / Biomarker Content of Review Report on TBCE Target / Biomarker
TBCE
Other Name(s): tubulin folding cofactor E | TBCE variant 3 | Tubulin folding cofactor E, transcript variant 3 | Tubulin folding cofactor E, transcript variant 1 | Tubulin-specific chaperone E | hypoparathyroidism, growth and mental retardation, and dysmorphism | TBCE variant 1 | PEAMO | KCS1 | pac2 | Hypoparathyroidism, growth and mental retardation, and dysmorphism | KCS | HRD | Tubulin-specific chaperone E (isoform a) | Tubulin-specific chaperone E (isoform b) | Pac2 | TBCE_HUMAN | Tubulin-folding cofactor E

TBCE: A Potential Drug Target and Biomarker for the Treatment of Muscular Dystrophy

Muscular dystrophy is a group of genetic disorders characterized by progressive muscle weakness and degenerative changes. It affects millions of people worldwide, ranging from infancy to adulthood, and can significantly impact an individual's quality of life. Despite the increasing number of therapeutic options available for muscular dystrophy, the treatment options remain limited, and there is a growing need for new, more effective approaches.

Tubulin folding cofactor E (TBCE), a protein that plays a crucial role in the regulation of microtubules, has recently been identified as a potential drug target and biomarker for the treatment of muscular dystrophy. In this article, we will explore the role of TBCE in the development and progression of muscular dystrophy, its potential as a drug target, and its potential as a biomarker for the assessment of disease severity and response to therapy.

The Role of TBCE in Muscular Dystrophy

Muscular dystrophy is a group of genetic disorders characterized by the progressive loss of muscle mass and strength. The most common form of muscular dystrophy is dystrophin-deficient dystrophy (DDD), caused by the absence of dystrophin, a protein that helps keep muscle cells intact. The loss of dystrophin leads to the breakdown of muscle cells, leading to progressive muscle weakness and degenerative changes.

Tubulin folding cofactor E (TBCE) is a protein that plays a crucial role in the regulation of microtubules, which are the structural scaffolding of cells. Microtubules are made up of a protein called tubulin and a protein called tau. The regulation of microtubules is critical for the proper functioning of cells, including the growth, division, and movement of cells.

In DDD, the loss of dystrophin leads to the breakdown of microtubules, leading to the misfunctioning of cells. TBCE has been shown to play a critical role in the regulation of microtubules and has been linked to the development and progression of DDD.

Potential Drug Target

TBCE has been identified as a potential drug target for the treatment of muscular dystrophy due to its role in the regulation of microtubules. The misfunctioning of microtubules in DDD leads to the breakdown of muscle cells, leading to progressive muscle weakness and degenerative changes. By targeting TBCE, researchers have the potential to improve muscle function and quality of life in individuals with DDD.

Potential Biomarker

TBCE has also been identified as a potential biomarker for the assessment of disease severity and response to therapy in DDD. The loss of dystrophin leads to the breakdown of microtubules, leading to the misfunctioning of cells. By measuring the levels of TBCE in muscle biopsy samples, researchers have the potential to assess the severity of DDD and the response to therapeutic interventions.

Conclusion

Tubulin folding cofactor E (TBCE) has recently been identified as a potential drug target and biomarker for the treatment of muscular dystrophy. The loss of dystrophin leads to the breakdown of microtubules, leading to the misfunctioning of cells. By targeting TBCE, researchers have the potential to improve muscle function and quality of life in individuals with DDD. Additionally, TBCE has also been identified as a potential biomarker for the assessment of disease severity and response to therapeutic interventions in DDD. Further research is needed to determine the effectiveness of TBCE as a therapeutic approach for

Protein Name: Tubulin Folding Cofactor E

Functions: Tubulin-folding protein; involved in the second step of the tubulin folding pathway and in the regulation of tubulin heterodimer dissociation. Required for correct organization of microtubule cytoskeleton and mitotic splindle, and maintenance of the neuronal microtubule network

The "TBCE 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 TBCE 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

TBCEL | TBCK | TBILA | TBK1 | TBKBP1 | TBL1X | TBL1XR1 | TBL1Y | TBL2 | TBL3 | TBP | TBPL1 | TBPL2 | TBR1 | TBRG1 | TBRG4 | TBX1 | TBX10 | TBX15 | TBX18 | TBX18-AS1 | TBX19 | TBX2 | TBX20 | TBX21 | TBX22 | TBX3 | TBX4 | TBX5 | TBX5-AS1 | TBX6 | TBXA2R | TBXAS1 | TBXT | TC2N | TCAF1 | TCAF1P1 | TCAF2 | TCAIM | TCAM1P | TCAP | TCEA1 | TCEA1P2 | TCEA2 | TCEA3 | TCEAL1 | TCEAL2 | TCEAL3 | TCEAL4 | TCEAL5 | TCEAL6 | TCEAL7 | TCEAL8 | TCEAL9 | TCEANC | TCEANC2 | TCERG1 | TCERG1L | TCF12 | TCF12-DT | TCF15 | TCF19 | TCF20 | TCF21 | TCF23 | TCF24 | TCF25 | TCF3 | TCF4 | TCF7 | TCF7L1 | TCF7L2 | TCFL5 | TCHH | TCHHL1 | TCHP | TCIM | TCIRG1 | TCL1A | TCL1B | TCL6 | TCN1 | TCN2 | TCOF1 | TCP1 | TCP10L | TCP10L2 | TCP10L3 | TCP11 | TCP11L1 | TCP11L2 | TCP11X2 | TCTA | TCTE1 | TCTN1 | TCTN2 | TCTN3 | TDG | TDGF1 | TDGF1P3