Identification of abnormal chromosomal complement in formalin‐fixed, paraffin‐embedded placental tissue

作者: Tracy A. Cowles , Frederick F. B. Elder , Suzanne Taylor

DOI: 10.1002/PD.1970150106

关键词:

摘要: The objective of this project was to assess the efficacy fluorescence in situ hybridization (FISH) with chromosome-specific DNA probes identify chromosome number formalin-fixed, paraffin-embedded placental specimens. Using approach, 75 per cent karyotypes 20 formalin-fixed samples (comprising aneuploids, triploids, and normals) were correctly identified. As technology improves, ability obtain information regarding chromosomal abnormalities tissue should improve as well. This can potentially provide important cytogenetic even when fresh is not available for standard karyotypic analysis.

参考文章(13)
Timothy Houseal, William Dackowski, Robert Harvey, Katherine Klinger, Donna Shook, Greg Landes, Benjamin Leverone, Terry Lerner, Linda Lopez, Pat Locke, Karen Pavelka, Rapin Osathanondh, Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH) American Journal of Human Genetics. ,vol. 51, pp. 55- 65 ,(1992)
B C McGillivray, D K Kalousek, I J Barrett, Placental mosaicism and intrauterine survival of trisomies 13 and 18. American Journal of Human Genetics. ,vol. 44, pp. 338- 343 ,(1989)
Wonbae Lee, Kyungja Han, Charles P. Harris, Lorraine F. Meisner, Detection of aneuploidy and possible deletion in paraffin-embedded rhabdomyosarcoma cells with FISH Cancer Genetics and Cytogenetics. ,vol. 68, pp. 99- 103 ,(1993) , 10.1016/0165-4608(93)90004-6
Sandra R. Wolman, Frederic M. Waldman, Margit Balazs, Complementarity of interphase and metaphase chromosome analysis in human renal tumors. Genes, Chromosomes and Cancer. ,vol. 6, pp. 17- 23 ,(1993) , 10.1002/GCC.2870060105
Rosa M. Drut, Charles P. Harris, Ricardo Drut, Lorraine Meisner, Use of fluorescent in situ hybridization to detect trisomy 13 in archival tissues for cytogenetic diagnosis. Pediatric pathology / affiliated with the International Paediatric Pathology Association. ,vol. 12, pp. 799- 805 ,(1992) , 10.3109/15513819209024236
James O. Price, Sherman Elias, Stephen S. Wachtel, Katherine Klinger, Michael Dockter, Avirachan Tharapel, Lee P. Shulman, Owen P. Phillips, Carole M. Meyers, Donna Shook, Joe Leigh Simpson, Prenatal diagnosis with fetal cells isolated from maternal blood by multiparameter flow cytometry. American Journal of Obstetrics and Gynecology. ,vol. 165, pp. 1731- 1737 ,(1991) , 10.1016/0002-9378(91)90024-L
D W Hedley, M L Friedlander, I W Taylor, C A Rugg, E A Musgrove, Method for analysis of cellular DNA content of paraffin-embedded pathological material using flow cytometry Journal of Histochemistry and Cytochemistry. ,vol. 31, pp. 1333- 1335 ,(1983) , 10.1177/31.11.6619538
S McQuaid, G M Allan, Detection protocols for biotinylated probes: optimization using multistep techniques.: Journal of Histochemistry and Cytochemistry. ,vol. 40, pp. 569- 574 ,(1992) , 10.1177/40.4.1552190
Kapil Dhingra, Aysegul Sahin, Janet Supak, S. Y. Kim, Gabriel Hortobagyi, Walter N. Hittelman, Chromosome in situ hybridization on formalin-fixed mammary tissue using non-isotopic, non-fluorescent probes: technical considerations and biological implications. Breast Cancer Research and Treatment. ,vol. 23, pp. 201- 210 ,(1992) , 10.1007/BF01833516
A H Hopman, F C Ramaekers, E van Hooren, P G Vooijs, C A van de Kaa, Detection of numerical chromosome aberrations using in situ hybridization in paraffin sections of routinely processed bladder cancers. Modern Pathology. ,vol. 4, pp. 503- 513 ,(1991)