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Related Concept Videos

Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
Hepatitis01:25

Hepatitis

Hepatitis is an inflammatory condition of the liver most commonly caused by hepatotropic viruses (A–E), though non-infectious causes such as alcohol and drugs also exist.Hepatitis AHepatitis A virus (HAV) is a non-enveloped RNA virus of the Picornaviridae family. It is primarily transmitted via the fecal-oral route, typically through ingestion of contaminated food or water. After ingestion, HAV enters the bloodstream through the oropharynx or intestinal epithelium and reaches the liver. The...
Pharmacogenetics of Drug Transporters: P-Glycoprotein and Solute Carrier Transporters01:16

Pharmacogenetics of Drug Transporters: P-Glycoprotein and Solute Carrier Transporters

The pharmacogenetics of drug transporters is increasingly recognized as a critical factor influencing interindividual variability in drug absorption, distribution, and elimination. These membrane-bound proteins regulate drugs' movement across cellular barriers by actively pumping them out (efflux) or facilitating their uptake (influx). Among the major transporter families, ATP-binding cassette (ABC) and solute carrier (SLC) transporters play particularly prominent roles. Genetic polymorphisms...
Pharmacogenetics of Phase II Enzymes: N-acetyltransferase, Thiopurine S-methyltransferase, UDP-glucuronosyltransferase01:27

Pharmacogenetics of Phase II Enzymes: N-acetyltransferase, Thiopurine S-methyltransferase, UDP-glucuronosyltransferase

Phase II biotransformation reactions are essential for detoxifying and eliminating xenobiotics, including many pharmaceutical compounds. These reactions typically involve conjugation, the covalent attachment of polar endogenous groups such as glucuronic acid, sulfate, methyl, or acetyl moieties to functional groups introduced during Phase I metabolism. The resulting conjugates are more water-soluble, enabling efficient renal or biliary excretion.The major classes of Phase II enzymes include...
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu01:29

Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu

Genetic variations significantly influence drug response through pharmacokinetics, receptor interactions, and biologic milieu modifications. Pharmacokinetic alterations impact drug metabolism and clearance, affecting efficacy and toxicity. Variants in drug-metabolizing enzymes, such as CYP2C9 and CYP2C19, alter drug activation and elimination. For example, CYP2C9 loss-of-function variants require lower warfarin doses to prevent excessive bleeding, while CYP2C19 variants reduce clopidogrel...
Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...

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Updated: Jul 15, 2026

Real-Time Polymerase Chain Reaction-Based Detection and Quantification of Hepatitis B Virus DNA
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Real-Time Polymerase Chain Reaction-Based Detection and Quantification of Hepatitis B Virus DNA

Published on: December 15, 2023

SPP1 polymorphisms associated with HBV clearance and HCC occurrence.

Hyoung Doo Shin1, Byung Lae Park, Hyun Sub Cheong

  • 1Department of Genetic Epidemiology, SNP Genetics, Inc., Rm 1407, 14th floor, Complex B, WooLim Lion's Valley, 371-28, Gasan-Dong, Geumcheon-Gu, Seoul, 153-803, Republic of Korea.

International Journal of Epidemiology
|May 15, 2007
PubMed
Summary

Genetic variations in Secreted Phosphoprotein-1 (SPP1) are linked to hepatitis B virus (HBV) clearance and the onset of hepatocellular carcinoma (HCC). SPP1 polymorphisms may influence host susceptibility to HBV infection outcomes and HCC development.

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Analysis of HBV-Specific CD4 T-cell Responses and Identification of HLA-DR-Restricted CD4 T-Cell Epitopes Based on a Peptide Matrix
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Analysis of HBV-Specific CD4 T-cell Responses and Identification of HLA-DR-Restricted CD4 T-Cell Epitopes Based on a Peptide Matrix

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Real-Time Polymerase Chain Reaction-Based Detection and Quantification of Hepatitis B Virus DNA
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Analysis of HBV-Specific CD4 T-cell Responses and Identification of HLA-DR-Restricted CD4 T-Cell Epitopes Based on a Peptide Matrix
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Analysis of HBV-Specific CD4 T-cell Responses and Identification of HLA-DR-Restricted CD4 T-Cell Epitopes Based on a Peptide Matrix

Published on: October 20, 2021

Area of Science:

  • Genetics
  • Hepatology
  • Immunology

Background:

  • Secreted Phosphoprotein-1 (SPP1) is a phosphoprotein overexpressed in metastatic hepatocellular carcinoma (HCC).
  • SPP1's role in metastatic HCC suggests potential as a diagnostic marker and therapeutic target.
  • Investigating SPP1 genetic polymorphisms may reveal host genetic factors influencing HBV clearance and HCC.

Purpose of the Study:

  • To investigate the association between SPP1 genetic polymorphisms and hepatitis B virus (HBV) clearance.
  • To determine if SPP1 polymorphisms are linked to the occurrence and progression of hepatocellular carcinoma (HCC).
  • To explore SPP1 as a candidate gene in host genetic studies of HBV infection and HCC.

Main Methods:

  • Genotyping of five SPP1 genetic variants using TaqMan assay.
  • Association analysis of SPP1 polymorphisms with HBV clearance in a Korean cohort (n=1,069).
  • Cox relative hazard analysis to assess the impact of SPP1 variants on HCC occurrence age.

Main Results:

  • A common SPP1 haplotype (SPP1-ht2) was significantly associated with HBV clearance.
  • SPP1-ht2 genotype frequency was higher in chronic carriers (CC) than spontaneously recovered (SR) individuals (OR=1.44, P=0.006).
  • SPP1-ht2 and a specific variant (-1,800G>T) were associated with earlier HCC onset in chronic hepatitis patients (RH=1.85 for both).

Conclusions:

  • SPP1 genetic polymorphisms appear to be significant host genetic factors influencing HBV clearance.
  • SPP1 variants are associated with the age of HCC occurrence among patients with chronic hepatitis B.
  • These findings highlight SPP1's potential role in the pathogenesis of HBV infection outcomes and HCC development.