Family's History Based on the CDH1 Germline Variant (c.360delG) and a Suspected Hereditary Gastric Cancer Form.
Laura CaggiariMara FornasarigMariangela De ZorziRenato CannizzaroAgostino SteffanValli De RePublished in: International journal of molecular sciences (2020)
Hereditary diffuse gastric cancer (HDGC) is a cancer susceptibility syndrome caused by germline pathogenic variant in CDH1, the gene encoding E-cadherin. The germline loss-of-function variants are the only proven cause of the cancer syndrome HDGC, occurring in approximately 10-18% of cases and representing a helpful tool in genetic counseling. The current case reports the family history based on a CDH1 gene variant, c.360delG, p.His121Thr in a suspected family for hereditary gastric cancer form. This frameshift deletion generates a premature stop codon at the amino acid 214, which leads to a truncated E-cadherin protein detecting it as a deleterious variant. The present study expands the mutational spectra of the family with the CDH1 variant. Our results highlight the clinical impact of the reported CDH1 variant running in gastric cancer families.
Keyphrases
- copy number
- papillary thyroid
- genome wide
- amino acid
- case report
- dna repair
- pulmonary embolism
- gene expression
- squamous cell
- dna methylation
- oxidative stress
- high intensity
- small molecule
- lymph node metastasis
- transcription factor
- hiv infected
- protein protein
- men who have sex with men
- high grade
- molecular dynamics
- dna damage
- genome wide identification
- binding protein
- hiv testing