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Cytogenetic description of breast fibroadenomas: alterations related solely to proliferation?
Burbano, R. R; Lima, E. M; Khayat, A. S; Barbieri Neto, J; Cabral, I. R; Bastos Júnior, L; Bahia, M. O; Casartelli, C.
  • Burbano, R. R; Universidade de Säo Paulo. Faculdade de Medicina de Ribeiräo Preto. Departamento de Genética. Ribeiräo Preto. BR
  • Lima, E. M; Universidade Federal do Pará. Centro de Ciências Biológicas. Departamento de Biologia. Belém. BR
  • Khayat, A. S; Universidade Federal do Pará. Centro de Ciências Biológicas. Departamento de Biologia. Belém. BR
  • Barbieri Neto, J; Universidade de Säo Paulo. Faculdade de Medicina de Ribeiräo Preto. Departamento de Patologia. Ribeiräo Preto. BR
  • Cabral, I. R; Universidade Federal do Pará. Centro de Ciências Biológicas. Departamento de Genética. Belém. BR
  • Bastos Júnior, L; Instituto da Saúde da Mulher. Belém. BR
  • Bahia, M. O; Universidade Federal do Pará. Centro de Ciências Biológicas. Departamento de Patologia. Belém. BR
  • Casartelli, C; Universidade de Säo Paulo. Faculdade de Medicina de Ribeiräo Preto. Departamento de Genética. Ribeiräo Preto. BR
Braz. j. med. biol. res ; 34(8): 1003-1006, Aug. 2001. ilus, tab
Article in English | LILACS | ID: lil-290148
RESUMO
Twelve breast fibroadenomas were analyzed cytogenetically and only four were found to have clonal alterations. The presence of chromosomal alterations in fibroadenomas must be the consequence of the proliferating process and must not be related to the etiology of this type of lesion. In contrast, the few fibroadenomas that exhibit chromosomal alterations are likely to be those presenting a risk of neoplastic transformation. Clonal numerical alterations involved chromosomes 8, 18, 19, and 21. Of the chromosomal alterations found in the present study, only monosomy of chromosomes 19 and 21 has been reported in breast fibroadenomas. The loss of chromosome 21 was the most frequent alteration found in our sample. The study of benign proliferations and their comparison with chromosome alterations in their malignant counterparts ought to result in a better understanding of the genes acting on cell proliferation alone, and of the genes that cause these cells to exhibit varied behaviors such as recurrences, spontaneous regression and fast growth
Subject(s)
Full text: Available Index: LILACS (Americas) Main subject: Breast Neoplasms / Chromosome Aberrations / Fibroadenoma / Cytogenetic Analysis Type of study: Observational study / Prognostic study / Risk factors Limits: Adolescent / Adult / Female / Humans Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2001 Type: Article Affiliation country: Brazil Institution/Affiliation country: Instituto da Saúde da Mulher/BR / Universidade Federal do Pará/BR / Universidade de Säo Paulo/BR

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Full text: Available Index: LILACS (Americas) Main subject: Breast Neoplasms / Chromosome Aberrations / Fibroadenoma / Cytogenetic Analysis Type of study: Observational study / Prognostic study / Risk factors Limits: Adolescent / Adult / Female / Humans Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2001 Type: Article Affiliation country: Brazil Institution/Affiliation country: Instituto da Saúde da Mulher/BR / Universidade Federal do Pará/BR / Universidade de Säo Paulo/BR