Source:http://linkedlifedata.com/resource/pubmed/id/10337997
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
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| pubmed:dateCreated |
1999-6-21
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| pubmed:abstractText |
The chromosomes of 81 pediatric germ cell tumors (GCTs) were analyzed as part of two clinical treatment trials, INT-0098 and INT-0097, conducted by the Children's Cancer Group. The analysis of chromosome results showed differences with respect to sex, age, tumor location, and histology. Sixteen of 17 benign teratomas of infants and children less than 4 years old and from gonadal and extragonadal locations were chromosomally normal. Twenty-three malignant GCTs from gonadal and extragonadal locations of the same age group were endodermal sinus tumors and varied in their karyotypic findings. The most common abnormalities were gains of 1q and chromosome 3. Of eight benign ovarian teratomas from older girls, five with normal G-banded karyotypes were determined to be homozygous for Q-band heteromorphisms, suggesting a meiosis II error. Among the 12 malignant ovarian GCTs from older girls, the common abnormalities were loss of 1p/gain of 1q, +3, +8, +14, and +21. Four of eight extragonadal tumors from older boys demonstrated +21; one had +X. Five of the eight had associated constitutional chromosome abnormalities, including one trisomy 21 and three with Klinefelter syndrome. The testicular GCTs of adolescents had abnormalities resembling those found in adult testicular GCT, including near-triploidy, loss of chromosomes 11, 13, and 18, and gain of chromosomes 7, 8, the X chromosome, and an isochromosome 12p. The gain of an isochromosome 12p was only frequent in the tumors from adolescent boys. Deletion of 1p/gain of 1q and +3 were the most common abnormalities among the malignant tumors from both sexes.
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| pubmed:commentsCorrections | |
| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:status |
MEDLINE
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| pubmed:month |
Jun
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| pubmed:issn |
1045-2257
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| pubmed:author | |
| pubmed:issnType |
Print
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| pubmed:volume |
25
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
134-46
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| pubmed:dateRevised |
2007-11-15
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| pubmed:meshHeading |
pubmed-meshheading:10337997-Abdominal Neoplasms,
pubmed-meshheading:10337997-Adolescent,
pubmed-meshheading:10337997-Adult,
pubmed-meshheading:10337997-Age Factors,
pubmed-meshheading:10337997-Bone Neoplasms,
pubmed-meshheading:10337997-Child,
pubmed-meshheading:10337997-Child, Preschool,
pubmed-meshheading:10337997-Chromosome Aberrations,
pubmed-meshheading:10337997-Chromosome Disorders,
pubmed-meshheading:10337997-Chromosomes, Human, Pair 18,
pubmed-meshheading:10337997-Clinical Trials as Topic,
pubmed-meshheading:10337997-Female,
pubmed-meshheading:10337997-Humans,
pubmed-meshheading:10337997-Infant,
pubmed-meshheading:10337997-Infant, Newborn,
pubmed-meshheading:10337997-Karyotyping,
pubmed-meshheading:10337997-Male,
pubmed-meshheading:10337997-Neoplasms, Germ Cell and Embryonal,
pubmed-meshheading:10337997-Ovarian Neoplasms,
pubmed-meshheading:10337997-Ploidies,
pubmed-meshheading:10337997-Sacrococcygeal Region,
pubmed-meshheading:10337997-Sex Factors,
pubmed-meshheading:10337997-Testicular Neoplasms
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| pubmed:year |
1999
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| pubmed:articleTitle |
Chromosome abnormalities of eighty-one pediatric germ cell tumors: sex-, age-, site-, and histopathology-related differences--a Children's Cancer Group study.
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| pubmed:affiliation |
Children's Cancer Group, Arcadia, California, USA.
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| pubmed:publicationType |
Journal Article
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