Aberrant methylation of the CHFR gene in digestive tract cancer

Yuki Morioka1, Kenji Hibi, Mitsuru Sakai

  • 1Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya 466-8560, Japan.

Anticancer Research
|July 11, 2006
PubMed
Abstract

Insights

Aberrant methylation of the CHFR gene is common in esophageal and gastric cancers. This gene methylation occurs across all clinical stages, suggesting it may be an early event in cancer development.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Genetics

Background:

  • Aberrant methylation of the CHFR gene is linked to gene silencing in various cancers.
  • The CHFR gene's methylation status was investigated in esophageal and gastric carcinomas.

Purpose of the Study:

  • To examine the methylation status of the CHFR gene in primary esophageal and gastric cancers.
  • To correlate CHFR gene methylation with clinicopathological findings.

Main Methods:

  • CHFR promoter methylation and mRNA expression analyzed in cancer cell lines.
  • CHFR gene methylation assessed in 38 esophageal and 53 gastric cancer samples.
  • Correlation analysis between CHFR methylation and clinicopathological data performed.

Main Results:

  • CHFR gene aberrant methylation detected in 24% of esophageal and 30% of gastric cancers.
  • Female esophageal cancers showed significantly higher methylation rates than male cancers (p = 0.0404).
  • Abnormal CHFR methylation was observed across all clinical stages for both cancer types.

Conclusions:

  • Frequent aberrant methylation of the CHFR gene observed in esophageal and gastric cancers.
  • CHFR gene methylation occurs at all clinical stages, indicating potential early-stage involvement.
  • CHFR methylation may serve as an early biomarker for esophageal and gastric cancers.

Related Concept Videos

Epigenetic Regulation01:37

Epigenetic Regulation

Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
Epigenetic Regulation01:46

Epigenetic Regulation

Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
Abnormal Proliferation02:23

Abnormal Proliferation

Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the daughter...
Mismatch Repair01:20

Mismatch Repair

Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase01:11

Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase

Genetic polymorphisms in drug targets have emerged as critical determinants of interindividual variability in drug response and toxicity. Pharmacogenomic investigations increasingly focus on identifying these variations to personalize and optimize therapeutic interventions. A drug target may be a receptor, enzyme, or signaling protein involved in pharmacologic responses or disease-related pathways. While early pharmacogenetic studies focused primarily on drug metabolism, current research...
Genomic Imprinting and Inheritance02:30

Genomic Imprinting and Inheritance

Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...