Document Detail

Hypothesis: meiotic origin of trisomic neoplasms.
MedLine Citation:
PMID:  8242589     Owner:  NLM     Status:  MEDLINE    
The gain of single additional chromosomes is a very common finding among the nonrandom abnormalities with human neoplasms. According to the current opinion, such trisomies result from a disease-related mitotic nondisjunction. In contrast, we suggest that some of these trisomies may in fact represent tissue-confined residual cell populations of meiotic origin. Our hypothesis is based on recent findings of uniparental disomies in humans (i.e., two homologous chromosomes are derived from the same parent) and on the notion that many of these disomies probably are the result of the successful correction of an initially trisomic conceptus. Thus, the trisomic neoplasm may represent the original trisomic karyotype, whereas the apparently normal disomic constitutional karyotype may be the acquired, corrected one. We propose molecular genetic strategies to test our hypothesis and suggest that constitutional uniparental disomies may be associated with an increased probability of developing neoplastic diseases characterized by trisomies for the respective chromosomes.
O A Haas; M Seyger
Related Documents :
10422809 - Pure trisomy 10p involving an isochromosome 10p.
6188379 - Brief clinical report: del(x) (q26) in a phenotypically normal woman and her daughter w...
10924569 - Echogenic intracardiac focus in 2nd-trimester fetuses with trisomy 21: usefulness as a ...
12975789 - Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.
1466569 - Trisomy 18q: 46,xx,-10,+der(10) t(10;18) (p15;q12) pat: a case report.
2945509 - 46,xx,t(15;21)/47,xx,15p-,+21 mosaicism in a child with down's syndrome.
2830469 - Use of recombination techniques to examine the structure of the csg locus of myxococcus...
7877949 - Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenata...
740059 - Some characteristics of karyotype changes in the nk/ly ascites tumor during its growth.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Cancer genetics and cytogenetics     Volume:  70     ISSN:  0165-4608     ISO Abbreviation:  Cancer Genet. Cytogenet.     Publication Date:  1993 Oct 
Date Detail:
Created Date:  1993-12-30     Completed Date:  1993-12-30     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  7909240     Medline TA:  Cancer Genet Cytogenet     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  112-6     Citation Subset:  IM    
CCRI, Children's Cancer Research Institute, Vienna, Austria.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Meiosis / genetics*
Models, Biological
Neoplasms / genetics*
Nondisjunction, Genetic
Comment In:
Cancer Genet Cytogenet. 1994 Sep;76(2):158   [PMID:  7923070 ]
Cancer Genet Cytogenet. 1994 Dec;78(2):242   [PMID:  7828161 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Cosmid mapping and locus linkage within the human chromosomal region 22q13.1.
Next Document:  Therapy-related myelodysplastic syndrome. Two cytogenetically unrelated abnormal clones in a patient...