Literature DB >> 8402545

Cytogenetic homogeneity in eight independent sites in a case of malignant melanoma.

H G Morse1, G E Moore.   

Abstract

Melanoma cell lines initiated from metastases excised at the same time from multiple sites in a patient reflect a single clone origin. The similarities of the karyotypes of these lines depend upon the site of excision, the selective survival in vitro, and the time span in vitro before study. In the present investigation, eight short-term cultures of malignant melanoma from the same patient were analyzed cytogenetically, six after the second passage in vitro, one from the third, and one from the fifth passage. Karyotypes were similar on all eight cultures, each having chromosome abnormalities der(1)t(1q;?), der(3)t(1;3), and t(7;9). Four cell lines had an isochromosome 4q, which was missing in four lines. Two cell lines were missing del(6). In five of eight cultures there was an occasional i(16q) or t(16q;21q). In the final culture, made 6 months after the first seven, three cell types present included a type corresponding to that of seven previous cultures, a similar cell type with an abnormal chromosome 11, and a third cell type with a 3;19 translocation. Comparisons are made with similar studies in the literature and a hypothesis has been formulated to explain melanoma metastases as revealed by the cytogenetics of multiple lesions excised simultaneously.

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Mesh:

Year:  1993        PMID: 8402545     DOI: 10.1016/0165-4608(93)90083-x

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  6 in total

1.  Chromosome 7 aneusomy. A marker for metastatic melanoma? Expression of the epidermal growth factor receptor gene and chromosome 7 aneusomy in nevi, primary malignant melanomas and metastases.

Authors:  M Udart; J Utikal; G M Krähn; R U Peter
Journal:  Neoplasia       Date:  2001 May-Jun       Impact factor: 5.715

2.  A comprehensive catalogue of somatic mutations from a human cancer genome.

Authors:  Erin D Pleasance; R Keira Cheetham; Philip J Stephens; David J McBride; Sean J Humphray; Chris D Greenman; Ignacio Varela; Meng-Lay Lin; Gonzalo R Ordóñez; Graham R Bignell; Kai Ye; Julie Alipaz; Markus J Bauer; David Beare; Adam Butler; Richard J Carter; Lina Chen; Anthony J Cox; Sarah Edkins; Paula I Kokko-Gonzales; Niall A Gormley; Russell J Grocock; Christian D Haudenschild; Matthew M Hims; Terena James; Mingming Jia; Zoya Kingsbury; Catherine Leroy; John Marshall; Andrew Menzies; Laura J Mudie; Zemin Ning; Tom Royce; Ole B Schulz-Trieglaff; Anastassia Spiridou; Lucy A Stebbings; Lukasz Szajkowski; Jon Teague; David Williamson; Lynda Chin; Mark T Ross; Peter J Campbell; David R Bentley; P Andrew Futreal; Michael R Stratton
Journal:  Nature       Date:  2009-12-16       Impact factor: 49.962

3.  Expression of NM23 in human melanoma progression and metastasis.

Authors:  D J Easty; K Maung; I Lascu; M Véron; M E Fallowfield; I R Hart; D C Bennett
Journal:  Br J Cancer       Date:  1996-07       Impact factor: 7.640

4.  PCR-Free Enrichment of Mitochondrial DNA from Human Blood and Cell Lines for High Quality Next-Generation DNA Sequencing.

Authors:  Meetha P Gould; Colleen M Bosworth; Sarah McMahon; Sneha Grandhi; Brian T Grimberg; Thomas LaFramboise
Journal:  PLoS One       Date:  2015-10-21       Impact factor: 3.240

5.  Deep convolutional neural networks for accurate somatic mutation detection.

Authors:  Sayed Mohammad Ebrahim Sahraeian; Ruolin Liu; Bayo Lau; Karl Podesta; Marghoob Mohiyuddin; Hugo Y K Lam
Journal:  Nat Commun       Date:  2019-03-04       Impact factor: 14.919

6.  An ensemble approach to accurately detect somatic mutations using SomaticSeq.

Authors:  Li Tai Fang; Pegah Tootoonchi Afshar; Aparna Chhibber; Marghoob Mohiyuddin; Yu Fan; John C Mu; Greg Gibeling; Sharon Barr; Narges Bani Asadi; Mark B Gerstein; Daniel C Koboldt; Wenyi Wang; Wing H Wong; Hugo Y K Lam
Journal:  Genome Biol       Date:  2015-09-17       Impact factor: 13.583

  6 in total

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