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M. Muleris, A. Dutrillaux, R. Salmon, B. Dutrillaux (1990)
Sex chromosomes in a series of 79 colorectal cancers: Replication pattern, numerical, and structural changesGenes, 1
J. Limon, K. Mrózek, S. Heim, P. Elfving, B. Nedoszytko, M. Babińska, N. Mandahl, R. Lundgren, F. Mitelman (1990)
On the significance of trisomy 7 and sex chromosome loss in renal cell carcinoma.Cancer genetics and cytogenetics, 49 2
R. Casalone, P. Simi, P. Granata, E. Minelli, A. Giudici, G. Butti, C. Solero (1990)
Correlation between cytogenetic and histopathological findings in 65 human meningiomas.Cancer genetics and cytogenetics, 45 2
Cigudosa JC. Lundgren R,
R. Berger, A. Bernheim (1979)
Y chromosome loss in leukemiasCancer Genetics and Cytogenetics, 1
M. Hollstein, R. Metcalf, J. Welsh, R. Montesano, C. Harris (1990)
Frequent mutation of the p53 gene in human esophageal cancer.Proceedings of the National Academy of Sciences of the United States of America, 87 24
H. Garewal, R. Sampliner, Yun Liu, J. Trent (1989)
Chromosomal rearrangements in Barrett's esophagus. A premalignant lesion of esophageal adenocarcinoma.Cancer genetics and cytogenetics, 42 2
Michel Robaszkiewicz, Brian Reid, Alain Volant, J. Cauvin, Peter Rabinovitch, Hervé Gouérou (1991)
Flow-cytometric DNA content analysis of esophageal squamous cell carcinomas.Gastroenterology, 101 6
E. Rodriguez, P. Rao, M. Ladanyi, N. Altorki, A. Albino, D. Kelsen, S. Jhanwar, R. Chaganti (1990)
11p13-15 is a specific region of chromosomal rearrangement in gastric and esophageal adenocarcinomas.Cancer research, 50 19
C. Tyler-Smith, Lesley Taylor, U. Müller (1988)
Structure of a hypervariable tandemly repeated DNA sequence on the short arm of the human Y chromosome.Journal of molecular biology, 203 4
(1984)
, 4, Fourth International Workshop on Chromosomes in Leu-kemia 1982 (
R. Boynton, Ying Huang, Patricia Blount, B. Reid, W. Raskind, R. Haggitt, C. Newkirk, J. Resau, Jing Yin, T. McDaniel, S. Meltzer (1991)
Frequent loss of heterozygosity at the retinoblastoma locus in human esophageal cancers.Cancer research, 51 20
(1989)
The neoplastic esophagus
A. Brothman, D. Peehl, Ankita Patel, J. McNeal (1990)
Frequency and pattern of karyotypic abnormalities in human prostate cancer.Cancer research, 50 12
R. Casalone, E. Minelli, P. Portensoso, A. Giudici (1990)
Clonal duplication of the Y chromosome and fra(X)(q28) in a case of epidermoid carcinoma of the esophagus.Cancer genetics and cytogenetics, 45 2
S. Heim, N. Mandahl, Yuesheng Jin, S. Strömblad, E. Lindstrom, L. Salford, F. Mitelman (1989)
Trisomy 7 and sex chromosome loss in human brain tissue.Cytogenetics and cell genetics, 52 3-4
J. Whang‐Peng, S. Banks-Schlegel, E. Lee (1990)
Cytogenetic studies of esophageal carcinoma cell lines.Cancer genetics and cytogenetics, 45 1
Chris Tyler-Smith, William Brown (1987)
Structure of the major block of alphoid satellite DNA on the human Y chromosome.Journal of molecular biology, 195 3
R. Pierre, H. Hoagland (1972)
Age‐associated aneuploidy: Loss of Y chromosome from human bone marrow cells with agingCancer, 30
P. Dileo, H. Müller, H. Obrecht, B. Speck, E. Bühler, G. Stalder (1977)
Loss of the Y chromosome from bone marrow cells of males with myeloproliferative disorders. Report of two cases and review of the literature.Acta haematologica, 57 5
C. Herrington, J. Burns, A. Graham, B. Bhatt, J. McGee (1989)
Interphase cytogenetics using biotin and digoxigenin labelled probes II: Simultaneous differential detection of human and papilloma virus nucleic acids in individual nuclei.Journal of Clinical Pathology, 42
S. Meltzer, Jing Yin, Ying Huang, T. McDaniel, C. Newkirk, O. Iseri, B. Vogelstein, J. Resau (1991)
Reduction to homozygosity involving p53 in esophageal cancers demonstrated by the polymerase chain reaction.Proceedings of the National Academy of Sciences of the United States of America, 88 11
A. Saadi, F. Latimer, M. Madercic, T. Robbins (1987)
Cytogenetic studies of human brain tumors and their clinical significance. II. Meningioma.Cancer genetics and cytogenetics, 26 1
C. Ohye, T. Shibazaki, T. Hirai, M. Matsumura, Y. Kawashima, M. Hirato (1989)
Microrecording for the study of thalamic organization, for tumor biopsy and removal.Stereotactic and functional neurosurgery, 52 2-4
E. Lindström, L. Salford, S. Heim, N. Mandahl, S. Strömblad, A. Brun, F. Mitelman (1991)
Trisomy 7 and Sex Chromosome Loss Need Not Be Representative of Tumor Parenchyma Cells in Malignant GliomaGenes, 3
P. Elfving, J. Cigudosa, R. Lundgren, J. Limon, N. Mandahl, U. Kristoffersson, S. Heim, F. Mitelman (1990)
Trisomy 7, trisomy 10, and loss of the Y chromosome in short-term cultures of normal kidney tissue.Cytogenetics and cell genetics, 53 2-3
K. United (1992)
Loss of the Y chromosome from normal and neoplastic bone marrowsGenes, 5
M. Wada, J. Yokota, H. Mizoguchi, M. Terada, Takashi Sugimura (1987)
Y chromosome abnormality in human stomach and lung cancer.Japanese journal of cancer research : Gann, 78 8
W. Raskind, T. Norwood, D. Levine, R. Haggitt, P. Rabinovitch, B. Reid (1992)
Persistent clonal areas and clonal expansion in Barrett's esophagus.Cancer research, 52 10
A. Hagemeijer, O. Garson, K. Kondo (1984)
Translocation (8;21)(q22;q22) in Acute Nonlymphocytic LeukemiaCancer Genetics and Cytogenetics, 11
H. Dekken, J. Pizzolo, D. Kelsen, M. Melamed (1990)
Targeted cytogenetic analysis of gastric tumors by in situhybridization with a set of chromosome‐specific dna probesCancer, 66
(1985)
Chromosome study
E. Unger, D. Brigati, M. Chenggis, L. Budgeon, D. Koebler, C. Cuomo, Tom Kennedy (1988)
Automation of In situ Hybridization: Application of the Capillary Action Robotic WorkstationJournal of Histotechnology, 11
(1982)
Characterization of a human Y chromosome repeated sequence and related sequences
Carcinoma of the esophagus shows a strong male predominance and other epidemiologic differences from cancers arising at other sites. In this study, the prevalence of Y chromosome loss in 29 carcinomas of the esophagus and 53 carcinomas arising elsewhere in the aerodigestive tract was assessed by in situ hybridization of formalin‐fixed paraffin‐embedded tissue sections. Absence of the Y chromosome was defined as (1) negative staining for Y in neoplastic cells with positive staining for Y in immediately adjacent nonneoplastic epithelial and stromal cells, (2) positive staining of neoplastic cells with control probes for chromosomes X and 17, and (3) similar results at different stringencies and levels of protein digestion. According to these criteria, absence of the Y chromosome was observed in 13 of 14 (93%) adenocarcinomas of the esophagus, 8 of 13 (62%) squamous cell carcinomas of the esophagus, and 5 of 53 (9%) carcinomas arising in other sites. For the neoplasms examined, Y chromosome deletion was strongly and selectively associated with carcinomas, particularly adenocarcinomas, of the esophagus (P < .0001). These findings suggest that Y chromosome loss may be pathogenetically significant in these neoplasms. © 1993 Wiley‐Liss, Inc.
Genes, Chromosomes and Cancer – Wiley
Published: Nov 1, 1993
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