Tylosis esophageal cancer locus on chromosome 17q25

Slides:



Advertisements
Similar presentations
Genetic testing for high-risk colon cancer patients1 William M. Grady Gastroenterology Volume 124, Issue 6, Pages (May 2003) DOI: /S (03)
Advertisements

Tylosis esophageal cancer locus on chromosome 17q25
Allan Balmain, Hiroki Nagase  Trends in Genetics 
Detection of 1p and 19q Loss in Oligodendroglioma by Quantitative Microsatellite Analysis, a Real-Time Quantitative Polymerase Chain Reaction Assay  Janice.
It's time to bring the best and brightest back to gastroenterology!
KLF4 is a Novel Candidate Tumor Suppressor Gene in Pancreatic Ductal Carcinoma  Francesca Zammarchi, Mariangela Morelli, Michele Menicagli, Claudio Di.
Stephen R. Broderick, MD, MPHS 
Novel Functional Single Nucleotide Polymorphisms in the Latent Transforming Growth Factor-β Binding Protein-1L Promoter  Tomomi Higashi, Satoru Kyo, Masaki.
Novel PMS2 Pseudogenes Can Conceal Recessive Mutations Causing a Distinctive Childhood Cancer Syndrome  Michel De Vos, Bruce E. Hayward, Susan Picton,
Volume 150, Issue 4, Pages (April 2016)
The Importance of Transurethral Resection in Managing Patients With Urothelial Cancer in the Bladder: Proposal for a Transurethral Resection of Bladder.
Distinguishing de Novo Second Cancer Formation from Tumor Recurrence
Volume 116, Issue 2, Pages (February 1999)
Somatic mutations in mitochondrial DNA do not associate with nuclear microsatellite instability in gastrointestinal cancer  Simó Schwartz, M.D., Ph.D.*,†,
Deficiency of the ADP-Forming Succinyl-CoA Synthase Activity Is Associated with Encephalomyopathy and Mitochondrial DNA Depletion  Orly Elpeleg, Chaya.
Volume 121, Issue 6, Pages (December 2001)
The BRCA1 suppressor hypothesis: An explanation for the tissue-specific tumor development in BRCA1 patients  Stephen J Elledge, Angelika Amon  Cancer.
Shaheen Alanee, Kasmintan Schrader, Kenneth Offit  European Urology 
Volume 126, Issue 4, Pages (April 2004)
Loss of Heterozygosity and Microsatellite Instability at theMLL Locus Are Common in Childhood Acute Leukemia, but not in Infant Acute Leukemia by Julie.
Volume 126, Issue 4, Pages (April 2004)
I. Silveira, I. Alonso, L. Guimarães, P. Mendonça, C. Santos, P
Volume 118, Issue 5, Pages (May 2000)
Volume 115, Issue 1, Pages (July 1998)
Ajay Goel, Takeshi Nagasaka, Jennifer Spiegel, Richard Meyer, Warren E
Volume 122, Issue 3, Pages (March 2002)
Volume 133, Issue 6, Pages (December 2007)
Molecular Cytogenetic Evidence for a Common Breakpoint in the Largest Inverted Duplications of Chromosome 15  A.E. Wandstrat, J. Leana-Cox, L. Jenkins,
This Month in Gastroenterology
Volume 124, Issue 3, Pages (March 2003)
Molecular Aspects of Melanocytic Dysplastic Nevi
Volume 117, Issue 4, Pages (October 1999)
De Novo BRCA1 Mutation in a Patient with Breast Cancer and an Inherited BRCA2 Mutation  Andrea Tesoriero, Chris Andersen, Melissa Southey, Gino Somers,
Clinical Categories of Neuroblastoma Are Associated with Different Patterns of Loss of Heterozygosity on Chromosome Arm 1p  Jaume Mora, Nai-Kong V. Cheung,
Kelsie L. Thu, BSc, Raj Chari, PhD, William W
Volume 119, Issue 3, Pages (September 2000)
PARP Inhibitors in Cancer Therapy: Promise, Progress, and Puzzles
Microsatellite Instability in Colorectal Cancer
Eung Bae Lee, MD, Tae I. n Park, MD, PhD, Sun H
Evidence for a Nonallelic Heterogeneity of Epidermodysplasia Verruciformis with Two Susceptibility Loci Mapped to Chromosome Regions 2p21–p24 and 17q25 
High Frequency of Loss of Heterozygosity on Chromosome Region 9p21–p22 but Lack of p16INK4a/p19ARF Mutations in Greek Patients with Basal Cell Carcinoma.
Activation of a Cryptic Splice Site of PTEN and Loss of Heterozygosity in Benign Skin Lesions in Cowden Disease  Stephen J. Meltzer, Manfred Wolter  Journal.
Molecular Diagnosis of Metastasizing Oligodendroglioma
Volume 122, Issue 5, Pages (May 2002)
A Multi-Exonic BRCA1 Deletion Identified in Multiple Families through Single Nucleotide Polymorphism Haplotype Pair Analysis and Gene Amplification with.
PARP Inhibitors in Cancer Therapy: Promise, Progress, and Puzzles
Volume 130, Issue 7, Pages (June 2006)
A Different Method in Diagnosis of Multiple Primary Lung Cancer
Molecular tracking of leukemogenesis in a triplet pregnancy
Volume 117, Issue 1, Pages (July 1999)
Localization of Multiple Melanoma Tumor–Suppressor Genes on Chromosome 11 by Use of Homozygosity Mapping-of-Deletions Analysis  Eleonora K. Goldberg,
Katy Hanlon, Lorna W. Harries, Sian Ellard, Claudius E. Rudin 
Stephen R. Broderick, MD, MPHS 
Novel PMS2 Pseudogenes Can Conceal Recessive Mutations Causing a Distinctive Childhood Cancer Syndrome  Michel De Vos, Bruce E. Hayward, Susan Picton,
A Novel Multiplexing, Polymerase Chain Reaction-Based Assay for the Analysis of Chromosome 18q Status in Colorectal Cancer  Nadina Erill, Anna Colomer,
Andrew Depiero, MDa. , Denise A. Kaminski, BSb, c. , John F
Overexpression of Wild-type p53 in Lichen Sclerosus adjacent to Human Papillomavirus-negative Vulvar Cancer  Katrina Vanin, James Scurry, Heather Thorne,
Janusz A. Jankowski, Dawn Provenzale, Paul Moayyedi  Gastroenterology 
Molecular Mechanisms Underlying Oncogenic RET Fusion in Lung Adenocarcinoma  Tatsuji Mizukami, MD, Kouya Shiraishi, PhD, Yoko Shimada, MFSc, Hideaki Ogiwara,
Xiangfeng Cui, Helen Feiner, Honghua Li 
Constitutional Mutations of the hSNF5/INI1 Gene Predispose to a Variety of Cancers  Nicolas Sévenet, Eammon Sheridan, Daniel Amram, Pascale Schneider,
A Deletion Mutation in COL17A1 in Five Austrian Families with Generalized Atrophic Benign Epidermolysis Bullosa Represents Propagation of an Ancestral.
Frequency and Carrier Risk Associated with Common BRCA1 and BRCA2 Mutations in Ashkenazi Jewish Breast Cancer Patients  Flora H. Fodor, Ainsley Weston,
Comparison of Genetic Profiles Between Primary Melanomas and their Metastases Reveals Genetic Alterations and Clonal Evolution During Progression  Reiji.
A New Familial Amyotrophic Lateral Sclerosis Locus on Chromosome 16q12
Measurement of Relative Copy Number of CDKN2A/ARF and CDKN2B in Bladder Cancer by Real-Time Quantitative PCR and Multiplex Ligation-Dependent Probe Amplification 
Representative images demonstrating LOH in breast cancer patients’ paired BM aspirate and primary tumors (T) at D14S62, D14S51, and D8S321, respectively.
Single nucleotide polymorphism array analysis can distinguish different genetic mechanisms that lead to loss of heterozygosity (LOH). Single nucleotide.
Fig. 7. JQ1 represses the enhancer-promoter interaction of BRCA1.
K. Miura, M. Obama, K. Yun, H. Masuzaki, Y. Ikeda, S. Yoshimura, T
Presentation transcript:

Tylosis esophageal cancer locus on chromosome 17q25 Tylosis esophageal cancer locus on chromosome 17q25.1 is commonly deleted in sporadic human esophageal cancer  Takeshi Iwaya*, Chihaya Maesawa*, Satoshi Ogasawara‡, Gen Tamura*  Gastroenterology  Volume 114, Issue 6, Pages 1206-1210 (June 1998) DOI: 10.1016/S0016-5085(98)70426-3 Copyright © 1998 American Gastroenterological Association Terms and Conditions

Fig. 1 Representative illustrations of microsatellite analysis in 4 patients (E74, E121, E115, and E59) with ESC. Arrowheads indicate the lost allele. N, normal DNA; T, tumor DNA. Gastroenterology 1998 114, 1206-1210DOI: (10.1016/S0016-5085(98)70426-3) Copyright © 1998 American Gastroenterological Association Terms and Conditions

Fig. 2 Results of PCR microsatellite assay on 17q in 43 ESCs exhibiting LOH and/or RER. Physical map of the microsatellite markers is shown at the lower side of the karyogram. Black and white boxes indicate LOH and retained heterozygosity, respectively. Blanks indicate noninformative markers. Group A (E17–126), total deletion; B (E7–119), LOH including both TOC and BRCA1; C (E16–121), tumors with LOH restricted at the TOC locus; D (E76–116 and E91–104), LOH at two or three distinct regions; E (E99 and 111), others. Gastroenterology 1998 114, 1206-1210DOI: (10.1016/S0016-5085(98)70426-3) Copyright © 1998 American Gastroenterological Association Terms and Conditions