Term
talking about a SINGLE GENE that gets mutated and will affect the drug response (ex: p53 tumor suppressor gene) |
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Definition
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Term
study of inter-individual variation in the whole genome and looking at candidate gene SNP maps, haplotype markers, and alteration in gene expression or inactivation that may be correlated with pharmacological function or therapeutic response |
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Definition
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Term
based on the whole genome, we have drugs that are targeted to certain genes and based on that gene sequence in a specific patient you can have a certain drug response in that patient |
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Definition
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Term
You can see which genes are affected by which drugs and this helps to identify if there are differences in your specific patient to avoid side effects, etc |
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Definition
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Term
Pharmacogenomics identifies biomarkers for diagnostic testing |
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Definition
identifies responders for early txt, excludes non-responders to avoid toxicities, lifts financial burden, enriches clinical trials of novel therapeutics |
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Term
defined as a variation in DNA sequence |
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Definition
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Term
if DNA variation present in less than 1% of population |
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Definition
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Term
if DNA variation present in more than 1% of population |
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Definition
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Term
SNPs, > 1 nt change, entire gene insertion/deletion, or extra copies of a gene |
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Definition
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Term
nomenclature: "VKORC2" from VKORC2 1173 C>T |
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Definition
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Term
nomenclature: "1173" from VKORC2 1173 C>T |
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Definition
indicates the nucleotide on the gene |
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Term
nomenclature: "C" from VKORC2 1173 C > T |
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Definition
represents the original (wild-type) nucleotide |
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Term
nomenclature: "T" from VKORC2 1173 C > T |
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Definition
represents the nucleotide that has changed to result in the SNP |
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Term
single database for all genetic variation information |
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Definition
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Term
the variant (and wild type) forms of a gene at a particular location on a chromosome |
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Definition
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Term
each individual carries 2 alleles of each gene; the 2 alleles that any individual has |
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Definition
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Term
set of alleles at multiple loci or areas of a gene that coexist on the same chromosome |
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Definition
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Term
when a higher frequency of the set of alleles co-exist than would be predicted by random chance |
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Definition
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Term
a single base substitution occurs within a gene; several million have been identified; may or may not alter protein synthesis |
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Definition
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Term
substitution of one base for another in an exon of a gene coding for a protein, such that the produced amino acid sequence is not modified |
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Definition
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Term
substitution of one base for another in an exon of a gene coding for a protein, such that the produced amino acid sequence is not modified |
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Definition
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Term
a change in amino acid that may result in a conservative, semi-conservative or radical change to the protein wild-type |
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Definition
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Term
proteins that contain oligosaccharide chains covalently attached to polypeptide side-chains |
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Definition
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Term
the carbohydrate is attached to the protein in a co-translational or posttranslational modification (glycoproteins) |
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Definition
glycosylation (plays a role in cell-cell interactions) |
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Term
Synonymous: SNP P-Glycoprotein (P-gp) affected drugs |
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Definition
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Term
Non-synonymous: SNP TPMT affected drugs |
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Definition
Azathioprine, 6-mercaptopurine |
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Term
There is a decreased conversion of 6-MP to its inactive metabolite and results in an INCREASE of thioguanine nucleotides (6-TGN) an active metabolites which will affect efficacy and toxicity |
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Definition
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Term
SNP CYP2C19 ---> CYP2C19*3 |
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Definition
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Term
results in no enzyme activity |
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Definition
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Term
Premature Stop Codon (CYP2C19*3) Affected Drugs |
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Definition
Proton Pump Inhibitors (Omeprazole, Lansooprazole) |
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Term
wild-type enzyme activity: cure rate of H. pylori for wild-type alleles is only around 20-30% due to a high metabolism of PPI into inactive metabolites |
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Definition
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Term
with somewhat reduced enzyme activity there is a slight buildup of drug and the cure rate of H. pylori is about 50-60% |
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Definition
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Term
major decrease in enzyme activity, resulting in a 14 fold increase in drug concentration and decreased metabolite concentration-- results in almost 100% cure rate of H. pylori |
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Definition
CYP2C19 *2/*2 or *2/*3 or *3/*3 |
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Term
Gene Deletion: CYP2D6 SNPs Affected Drugs |
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Definition
SSRIs, tamoxifen, codeine, beta-blockers |
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Term
not just a single nucleotide polymorphism, but thousands of nucleotide base pairs that comprise this gene are deleted |
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Definition
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Term
Function effect for CYP2D6*5 |
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Definition
Loss of function (or null activity); results in a poor metabolizer phenotype, the drug is not metabolized as well and there is buildup of these drugs in their system |
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Term
Copy Number Variant -- extra copies of this gene are present |
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Definition
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Term
With extra copies of the CYP2D6 gene |
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Definition
more enzymes present to break down the drug |
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Term
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Definition
ultra rapid metabolizer (UM) phenotype |
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Term
CYP2D6*2XN affected drugs |
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Definition
SSRIs, tamoxifen, codeine, beta-blockers |
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Term
higher frequency of the CYP2C19*3 allele |
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Definition
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Term
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Definition
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Term
Therapeutic Area Discussion Format |
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Definition
patient case, gene/allele of interest, functional effect, population prevalence, clinical relevance, genome test/testing recommendation, patient case summary |
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Term
human leukocyte antigen subclass B |
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Definition
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Term
Functional effect of HLA-B*5701 |
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Definition
high risk of abacavir-induced hypersensitivity reaction |
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Term
highest prevalence of HLA-B*5701 (5-8%) |
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Definition
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Term
can accurately predict patients who may be at risk for abacavir HSR |
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Definition
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Term
showed similar trend in whites and blacks; accurately predicted 100% of abacavir HSR cases |
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Definition
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Term
investigated HLA-B*5701 negative patients |
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Definition
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Term
HLA typing: positive test for HLA-B*5701 |
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Definition
confers an increased risk for HSR |
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