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Investigation of Genetic Association Between a High Activity Variant of Cathepsin G and Risk for Basal Cell Carcinoma.
Douka, Anna; Gintoni, Iphigenia; Derka, Spyridoula; Vairaktari, Georgia; Vassiliou, Stavros; Yapijakis, Christos.
Affiliation
  • Douka A; Unit of Orofacial Genetics, 1 Department of Pediatrics, National Kapodistrian University of Athens, "Hagia Sophia" Children's Hospital, Athens, Greece.
  • Gintoni I; Department of Molecular Genetics, Cephalogenetics Center, Athens, Greece.
  • Derka S; Unit of Orofacial Genetics, 1 Department of Pediatrics, National Kapodistrian University of Athens, "Hagia Sophia" Children's Hospital, Athens, Greece.
  • Vairaktari G; Department of Molecular Genetics, Cephalogenetics Center, Athens, Greece.
  • Vassiliou S; Department of Oral and Maxillofacial Surgery, School of Medicine, National and Kapodistrian University of Athens, Attikon Hospital, Athens, Greece.
  • Yapijakis C; Department of Oral and Maxillofacial Surgery, School of Medicine, National and Kapodistrian University of Athens, Attikon Hospital, Athens, Greece.
Anticancer Res ; 44(5): 2091-2094, 2024 May.
Article in En | MEDLINE | ID: mdl-38677729
ABSTRACT
BACKGROUND/

AIM:

Cathepsin G (CTSG) has been identified as an inhibitor of breast, bladder, and colorectal cancers. The G allele of the N125S (A/G, rs45567233) functional polymorphism of the CTSG gene confers increased serum CTSG activity and has been associated with cardiovascular and neurovascular diseases. This study examined the possible correlation between the pathogenesis of basal cell carcinoma (BCC) and the functional polymorphism CTSG N125S. PATIENTS AND

METHODS:

A total of 197 DNA samples were examined, comprising 98 BCC patients and 99 control samples of Greek origin. The CTSG N125S polymorphism was molecularly genotyped using PCR amplification, followed by enzyme digestion, and agarose gel electrophoresis of the amplified DNA fragments.

RESULTS:

There was no statistically significant difference in the genotypic and allelic frequencies between the patient and the control groups.

CONCLUSION:

There is no association between the CTSG N125S polymorphism and pathogenesis of BCC.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Basal Cell / Genetic Predisposition to Disease / Cathepsin G Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Anticancer Res Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Basal Cell / Genetic Predisposition to Disease / Cathepsin G Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Anticancer Res Year: 2024 Document type: Article Affiliation country: Country of publication: