PEDIATRICS Vol. 67 No. 1 January 1981, pp. 119-127
This Article
Right arrow Full Text (PDF)
Right arrow P3Rs: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when P3Rs are posted
Right arrow Alert me if a correction is posted
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cervenka, J.
Right arrow Articles by Yasis, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cervenka, J.
Right arrow Articles by Yasis, C.

Mitomycin C Test for Diagnostic Differentiation of Idiopathic Aplastic Anemia and Fanconi Anemia

Jaroslav Cervenka MD, CSc1, Diane Arthur MD1, and Carmen Yasis 1

1 Department of Oral Pathology and Genetics, School of Dentistry and Department of Pediatrics, Medical School, University of Minnesota, Minneapolis

A cytogenetic test was developed to enable the diagnostic differentiation between Fanconi anemia and the group of disorders classified as "idiopathic" aplastic anemia. The method is based on the effect of the bifunctional alkylating agent mitomycin C (MMC) on chromosomes of peripheral lymphocytes in culture 92 to 96 hours. At the highest concentration of 80 ng/ml of MMC, about a 50-fold increase of chromosomal breaks and a 200-fold increase of radial figures was observed in Fanconi anemia lymphocytes in comparison with the average values for aplastic anemia cells or cells of healthy control subjects. In addition, sister chromatid exchange analysis of cells treated with MMC demonstrated a marked inhibition of mitotic activity of lymphocytes of patients with increased sensitivity to MMC. It is advocated that the MMC-stress test should be used in each case of pancytopenia, as part of the therapy planning. The cytoreduction regimens used prior to bone marrow transplantation may produce lethal complications in patients with high clastogenic response to MMC.

Submitted on March 24, 1980
Accepted on May 19, 1980




This article has been cited by other articles:


Home page
Mol. Cell. Biol.Home page
J. L. Youds, L. J. Barber, J. D. Ward, S. J. Collis, N. J. O'Neil, S. J. Boulton, and A. M. Rose
DOG-1 Is the Caenorhabditis elegans BRIP1/FANCJ Homologue and Functions in Interstrand Cross-Link Repair
Mol. Cell. Biol., March 1, 2008; 28(5): 1470 - 1479.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
T. J. Vulliamy, A. Marrone, S. W. Knight, A. Walne, P. J. Mason, and I. Dokal
Mutations in dyskeratosis congenita: their impact on telomere length and the diversity of clinical presentation
Blood, April 1, 2006; 107(7): 2680 - 2685.
[Abstract] [Full Text] [PDF]


Home page
Arch Otolaryngol Head Neck SurgHome page
B. P. Alter, H. Joenje, A. B. Oostra, and G. Pals
Fanconi Anemia: Adult Head and Neck Cancer and Hematopoietic Mosaicism
Arch Otolaryngol Head Neck Surg, July 1, 2005; 131(7): 635 - 639.
[Full Text] [PDF]


Home page
BloodHome page
B. Hirsch, A. Shimamura, L. Moreau, S. Baldinger, M. Hag-alshiekh, B. Bostrom, S. Sencer, and A. D. D'Andrea
Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood
Blood, April 1, 2004; 103(7): 2554 - 2559.
[Abstract] [Full Text] [PDF]