Cytogenetic aberrations in primary cell cultures of the ovarian surface epithelium
Our objective was to determine the presence of chromosomal abnormalities in primary cultures of ovarian surface epithelial cells in women of different ages with no history of cancer. Throughout conventional cytogenetic techniques, we analyzed chromosome spreads of cultured ovarian epithelial cells f...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2010
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- spa
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/22188
- Acceso en línea:
- https://repository.urosario.edu.co/handle/10336/22188
- Palabra clave:
- Adult
Age distribution
Article
Cancer risk
Cell culture
Chromosomal instability
Chromosome 11
Chromosome 3
Chromosome aberration
Chromosome deletion
Clinical article
Colombia
Controlled study
Cytogenetics
Epithelium cell
Female
Genetic heterogeneity
Human
Human cell
Menopause
Metaphase
Monosomy
Ovary cell
Polyploidy
Population
Age
Aged
Aneuploidy
Cell culture
Cell transformation
Comparative study
Cytology
Disease predisposition
Genetics
Karyotyping
Middle aged
Mitosis index
Ovary
Ovary tumor
Postmenopause
Ultrastructure
Age factors
Aged
Aneuploidy
Chromosome aberrations
Disease susceptibility
Epithelial cells
Female
Humans
Karyotyping
Metaphase
Middle aged
Mitotic index
Ovarian neoplasms
Ovary
Postmenopause
Cell cultures
Chromosomal instability
Chromosome aberrations
Ovarian epithelium
Polyploidy
neoplastic
cultured
Cell transformation
Cells
- Rights
- License
- Abierto (Texto Completo)
Summary: | Our objective was to determine the presence of chromosomal abnormalities in primary cultures of ovarian surface epithelial cells in women of different ages with no history of cancer. Throughout conventional cytogenetic techniques, we analyzed chromosome spreads of cultured ovarian epithelial cells from 10 donors who were 50 or more years old (B) and 16 controls between 20 and 49 years old (A), belonging to the mestizo population in Bogota DC, Colombia. Of the 26 cultures that were analyzed in passage 1, 61.5% had an abnormal chromosome complement (62.5% in A, and 60% in B). Abnormalities included polyploidies, endoduplications and monosomies. Deletions in chromosomes 3 and 11 were found in just one metaphase. None of the samples showed weaknesses or breakpoints. After transforming and applying the exact student's t-test for variance heterogeneity, we found significant differences in the frequency of metaphases, that were higher in A than in B (p=0.05), and in the frequency of polyploidies, which were higher in B than in A (p=0.044). Through the application of the Mann-Whitney test, we determined that the frequency of endoduplications was higher in A than in B (p=0.126), without reaching significant differences. There were no significant differences in the frequency of monosomies. The level of significance was set at p ? 0.05. Taking into account that polyploidization is a marker of chromosomal instability and that the risk of cancer arising from the ovarian surface epithelium augments substantially after menopause, the increase in the frequency of age-associated polyploidies could be used as a predictor of ovarian cancer in women from an ethnically homogeneous population as the mestizo one in Bogota DC. |
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