Drug Target (Biomarker) DLD: Unlocking the Potential of Genomics
Drug Target (Biomarker) DLD: Unlocking the Potential of Genomics
The discovery of DNA-based diagnostics and therapies has revolutionized the field of medicine. One of the promising areas of study is the use of DNA as a drug target or biomarker. DNA-based biomarkers can provide valuable information about the disease process, treatment response, and patient outcomes. In this article, we will explore the concept of DNA-based drug targets and their potential as biomarkers in disease diagnosis and treatment.
What is a DNA-Based Drug Target?
A DNA-based drug target is a specific segment of DNA that is associated with the development or progression of a particular disease. These targets are derived from a patient's genetic makeup, and they can be used to develop new treatments or monitor disease progression. The use of DNA-based drug targets is also known as genetic engineering of the therapeutic index.
DNA-based drug targets can be segmented into two categories: either intracellular targets or extracellular targets. Intracellular targets are associated with the regulation of gene expression, while extracellular targets are associated with the regulation of protein activity.
The Potential of DNA-Based Drug Targets
The use of DNA-based drug targets has the potential to revolutionize the field of medicine. By developing new treatments based on DNA-based targets, doctors can improve patient outcomes and reduce the risk of relapse.
One of the major benefits of DNA-based drug targets is their specificity. Unlike many protein-based targets, DNA-based targets are much more stable and can be used to develop targeted treatments that are unlikely to have unintended effects on other parts of the body. This can reduce the risk of drug-related side effects and improve the overall quality of life for patients.
Another advantage of DNA-based drug targets is their ability to be used as biomarkers. By analyzing the genetic makeup of a patient, doctors can determine the presence or absence of a particular DNA-based target. This can be used to monitor disease progression and determine the effectiveness of a particular treatment.
DNA-Based Biomarkers
DNA-based biomarkers are used to monitor disease progression and assess the effectiveness of a particular treatment. These biomarkers are derived from a patient's DNA and can be used to detect changes in the disease process over time.
One of the major benefits of DNA-based biomarkers is their non-invasive nature. Unlike many other types of diagnostic tests, DNA-based biomarkers do not require a biopsy or other invasive procedures to be performed. This makes them a convenient and non-invasive option for monitoring disease progression.
DNA-Based Therapeutic Interventions
DNA-based therapeutic interventions are a type of cancer treatment that is derived from a patient's DNA. These interventions use the patient's own immune system to fight the cancer cells.
One of the major benefits of DNA-based therapeutic interventions is their ability to be customized to the individual patient. By analyzing the genetic makeup of the cancer cells, doctors can determine which DNA-based therapeutic intervention will be most effective for that particular patient. This can improve the effectiveness of the treatment and reduce the risk of relapse.
Conclusion
DNA-based drug targets and biomarkers have the potential to revolutionize the field of medicine. By developing new treatments based on DNA-based targets and using DNA-based biomarkers to monitor disease progression, doctors can improve patient outcomes and reduce the risk of relapse. As the field of DNA-based medicine continues to grow, we can expect to see even more innovative and effective treatments emerge.
Protein Name: Dihydrolipoamide Dehydrogenase
Functions: Lipoamide dehydrogenase is a component of the glycine cleavage system as well as an E3 component of three alpha-ketoacid dehydrogenase complexes (pyruvate-, alpha-ketoglutarate-, and branched-chain amino acid-dehydrogenase complex) (PubMed:15712224, PubMed:16442803, PubMed:16770810, PubMed:17404228, PubMed:20160912, PubMed:20385101). The 2-oxoglutarate dehydrogenase complex is mainly active in the mitochondrion (PubMed:29211711). A fraction of the 2-oxoglutarate dehydrogenase complex also localizes in the nucleus and is required for lysine succinylation of histones: associates with KAT2A on chromatin and provides succinyl-CoA to histone succinyltransferase KAT2A (PubMed:29211711). In monomeric form may have additional moonlighting function as serine protease (PubMed:17404228). Involved in the hyperactivation of spermatazoa during capacitation and in the spermatazoal acrosome reaction (By similarity)
More Common Targets
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 | DMBT1 | DMBT1L1 | DMBX1 | DMC1 | DMD | DMGDH | DMKN | DMP1 | DMPK | DMRT1 | DMRT2 | DMRT3 | DMRTA1 | DMRTA2 | DMRTB1 | DMRTC1 | DMRTC1B | DMRTC2 | DMTF1 | DMTF1-AS1 | DMTN | DMWD | DMXL1 | DMXL2 | DNA ligase | DNA Methyltransferase (DNMT) | DNA Polymerase alpha | DNA polymerase delta | DNA Polymerase epsilon | DNA Polymerase gamma | DNA Polymerase zeta Complex | DNA primase | DNA topoisomerase | DNA Topoisomerase II | DNA-Dependent Protein Kinase (DNA-PK) | DNA-Directed DNA Polymerase Complex | DNA-Directed RNA Polymerase | DNA-Directed RNA Polymerase I | DNA-Directed RNA Polymerase II | DNA-directed RNA polymerase II, core complex | DNA-directed RNA polymerase III | DNA2 | DNAAF1 | DNAAF10 | DNAAF11 | DNAAF2 | DNAAF3 | DNAAF4 | DNAAF4-CCPG1 | DNAAF5 | DNAAF6 | DNAAF8 | DNAAF9 | DNAH1 | DNAH10 | DNAH11 | DNAH12 | DNAH14