Molecular Diagnosis in Ewing Family Tumors

Slides:



Advertisements
Similar presentations
High-Quality Genotyping Data from Formalin-Fixed, Paraffin-Embedded Tissue on the Drug Metabolizing Enzymes and Transporters Plus Array  Hanneke I. Vos,
Advertisements

A Genome-Wide High-Resolution Array-CGH Analysis of Cutaneous Melanoma and Comparison of Array-CGH to FISH in Diagnostic Evaluation  Lu Wang, Mamta Rao,
Mutation Screening of EXT1 and EXT2 by Denaturing High-Performance Liquid Chromatography, Direct Sequencing Analysis, Fluorescence in Situ Hybridization,
Detection of TMPRSS2-ETS Fusions by a Multiprobe Fluorescence in Situ Hybridization Assay for the Early Diagnosis of Prostate Cancer  Qi-Peng Sun, Liao-Yuan.
Droplet Digital PCR for Absolute Quantification of EML4-ALK Gene Rearrangement in Lung Adenocarcinoma  Qiushi Wang, Xin Yang, Yong He, Qiang Ma, Li Lin,
Simultaneous Detection of Clinically Relevant Mutations and Amplifications for Routine Cancer Pathology  Marlous Hoogstraat, John W.J. Hinrichs, Nicolle.
Tracy I. George, Joanna E. Wrede, Charles D. Bangs, Athena M
RT-PCR Analysis of RNA Extracted from Bouin-Fixed and Paraffin-Embedded Lymphoid Tissues  Annunziata Gloghini, Barbara Canal, Ulf Klein, Luigino Dal Maso,
Molecular Diagnosis of Clear Cell Sarcoma
Detection of TMPRSS2-ETS Fusions by a Multiprobe Fluorescence in Situ Hybridization Assay for the Early Diagnosis of Prostate Cancer  Qi-Peng Sun, Liao-Yuan.
Genotyping of Chimerical BCR-ABL1 RNA in Chronic Myeloid Leukemia by Integrated DNA Chip  Jong-Hun Kang, Hyun-Gyung Goh, Sang-Ho Chae, Sung-Yong Kim,
A Case of FIP1L1-PDGFRA-Positive Chronic Eosinophilic Leukemia with a Rare FIP1L1 Breakpoint  Frédéric Lambert, Pierre Heimann, Christian Herens, Alain.
Hendrikus J. Dubbink, Peggy N. Atmodimedjo, Ronald van Marion, Niels M
A Single-Tube Multiplexed Assay for Detecting ALK, ROS1, and RET Fusions in Lung Cancer  Maruja E. Lira, Yoon-La Choi, Sun Min Lim, Shibing Deng, Donghui.
Molecular Genetics of Pediatric Soft Tissue Tumors
A Multiplex SNaPshot Assay as a Rapid Method for Detecting KRAS and BRAF Mutations in Advanced Colorectal Cancers  Sandrine Magnin, Erika Viel, Alice.
Carmo Martins, Branca Cavaco, Giovanni Tonon, Frederic J
Comprehensive Analysis of CBFβ-MYH11 Fusion Transcripts in Acute Myeloid Leukemia by RT-PCR Analysis  ShriHari S. Kadkol, Annette Bruno, Carol Dodge,
Jonathan A. Schumacher, Stephen D. Jenson, Kojo S. J
Tony L. Ng, Maureen J. O'Sullivan, Catherine J
IgH PCR of Zinc Formalin-Fixed, Paraffin-Embedded Non-Lymphomatous Gastric Samples Produces Artifactual “Clonal” Bands Not Observed in Paired Tissues.
Betaine, Dimethyl Sulfoxide, and 7-Deaza-dGTP, a Powerful Mixture for Amplification of GC-Rich DNA Sequences  Marco Musso, Renata Bocciardi, Sara Parodi,
FISH Analysis for the Detection of Lymphoma-Associated Chromosomal Abnormalities in Routine Paraffin-Embedded Tissue  Roland A. Ventura, Jose I. Martin-Subero,
Simultaneous Detection of Clinically Relevant Mutations and Amplifications for Routine Cancer Pathology  Marlous Hoogstraat, John W.J. Hinrichs, Nicolle.
Multiplex Ligation-Dependent Probe Amplification
CRISPR/Cas9 Technology–Based Xenograft Tumors as Candidate Reference Materials for Multiple EML4-ALK Rearrangements Testing  Rongxue Peng, Rui Zhang,
Characterization of the Different BCR-ABL Transcripts with a Single Multiplex RT-PCR  Jacques Chasseriau, Jérôme Rivet, Frédéric Bilan, Jean-Claude Chomel,
Molecular Diagnostic Approach to Non-Hodgkin's Lymphoma
Development and Verification of an RNA Sequencing (RNA-Seq) Assay for the Detection of Gene Fusions in Tumors  Jennifer L. Winters, Jaime I. Davila, Amber.
Single Monochrome Real-Time RT-PCR Assay for Identification, Quantification, and Breakpoint Cluster Region Determination of t(9;22) Transcripts  Marina.
Undifferentiated Small Round Cell Sarcomas with Rare EWS Gene Fusions
Sequencing of t(2;7) Translocations Reveals a Consistent Breakpoint Linking CDK6 to the IGK Locus in Indolent B-Cell Neoplasia  Edward P.K. Parker, Reiner.
Molecular Analysis of Gene Fusions in Bone and Soft Tissue Tumors by Anchored Multiplex PCR–Based Targeted Next-Generation Sequencing  Suk Wai Lam, Anne-Marie.
Sean C. Murphy, Daniel R. Hoogestraat, Dhruba J
Identification of Combinatorial Genomic Abnormalities Associated with Prostate Cancer Early Recurrence  Xiaoyu Qu, Claudio Jeldres, Lena Glaskova, Cynthia.
Hepatosplenic and Subcutaneous Panniculitis-Like γ/δ T Cell Lymphomas Are Derived from Different Vδ Subsets of γ/δ T Lymphocytes  Grzegorz K. Przybylski,
A Genome-Wide High-Resolution Array-CGH Analysis of Cutaneous Melanoma and Comparison of Array-CGH to FISH in Diagnostic Evaluation  Lu Wang, Mamta Rao,
High-Quality Genotyping Data from Formalin-Fixed, Paraffin-Embedded Tissue on the Drug Metabolizing Enzymes and Transporters Plus Array  Hanneke I. Vos,
Pathogenicity Evaluation of BRCA1 and BRCA2 Unclassified Variants Identified in Portuguese Breast/Ovarian Cancer Families  Catarina Santos, Ana Peixoto,
Development of an NPM1/MLF1 D-FISH Probe Set for the Detection of t(3;5)(q25;q35) Identified in Patients with Acute Myeloid Leukemia  Umut Aypar, Ryan.
Catherine E. Keegan, Anthony A. Killeen 
A Novel Mass Spectrometry–Based Assay for Diagnosis of EML4-ALK–Positive Non– Small Cell Lung Cancer  Kazuko Sakai, PhD, Isamu Okamoto, MD, PhD, Ken Takezawa,
Analysis of Rare APC Variants at the mRNA Level
Inconspicuous Insertion 22;12 in Myxoid/Round Cell Liposarcoma Accompanied by the Secondary Structural Abnormality der(16)t(1;16)  Nathan C. Birch, Cristina.
Benjamin P. Song, Surbhi Jain, Selena Y. Lin, Quan Chen, Timothy M
Diagnostic Utility of Molecular Investigation in Extraskeletal Myxoid Chondrosarcoma  Stefania Benini, Stefania Cocchi, Gabriella Gamberi, Giovanna Magagnoli,
PIK3CA Hotspot Mutation Scanning by a Novel and Highly Sensitive High-Resolution Small Amplicon Melting Analysis Method  Panagiotis A. Vorkas, Nikoleta.
The MECT1-MAML2 Gene Fusion and Benign Warthin's Tumor
The Molecular Pathology of Primary Immunodeficiencies
The Journal of Molecular Diagnostics
Molecular Pathology of Bone Tumors
A Multi-Exonic BRCA1 Deletion Identified in Multiple Families through Single Nucleotide Polymorphism Haplotype Pair Analysis and Gene Amplification with.
Evaluating the Effect of Unclassified Variants Identified in MMR Genes Using Phenotypic Features, Bioinformatics Prediction, and RNA Assays  Lucia Pérez-Cabornero,
Ye Bang-Ce, Chu Xiaohe, Fan Ye, Li Songyang, Yin Bincheng, Zuo Peng 
Detection of KIAA1549-BRAF Fusion Transcripts in Formalin-Fixed Paraffin-Embedded Pediatric Low-Grade Gliomas  Yongji Tian, Benjamin E. Rich, Natalie.
Mutation Detection of Epidermal Growth Factor Receptor and KRAS Genes Using the Smart Amplification Process Version 2 from Formalin-Fixed, Paraffin-Embedded.
Jianbo Song, Danielle Mercer, Xiaofeng Hu, Henry Liu, Marilyn M. Li 
The Detection of t(14;18) in Archival Lymph Nodes
Amplification and Overexpression of the EMS 1 Oncogene, a Possible Prognostic Marker, in Human Hepatocellular Carcinoma  Bao-Zhu Yuan, Xiaoling Zhou,
Gayatry Mohapatra, Rebecca A. Betensky, Ezra R
Development of Five Dual-Color, Double-Fusion Fluorescence in Situ Hybridization Assays for the Detection of Common MLL Translocation Partners  Jeannette.
ChildSeq-RNA The Journal of Molecular Diagnostics
JAZF1/JJAZ1 Gene Fusion in Endometrial Stromal Sarcomas
Characterization of messenger RNA expression of estrogen receptor-α and -β in patients with ovarian endometriosis  Sachiko Matsuzaki, M.D., Takao Fukaya,
Extensive Molecular Analysis of Patients Bearing CFTR-Related Disorders  Felice Amato, Chiara Bellia, Giuseppe Cardillo, Giuseppe Castaldo, Marcello Ciaccio,
Fluorescence In Situ Hybridization Identifies Cryptic t(16;16)(p13;q22) Masked By del(16)(q22) in a Case of AML-M4 Eo  Shakil H. Merchant, Skip Haines,
Xiangfeng Cui, Helen Feiner, Honghua Li 
Maureen J. O'Sullivan, Peter A. Humphrey, Louis P. Dehner, John D
Measurement of Relative Copy Number of CDKN2A/ARF and CDKN2B in Bladder Cancer by Real-Time Quantitative PCR and Multiplex Ligation-Dependent Probe Amplification 
Preanalytic Variables and Tissue Stewardship for Reliable Next-Generation Sequencing (NGS) Clinical Analysis  Paolo A. Ascierto, Carlo Bifulco, Giuseppe.
Presentation transcript:

Molecular Diagnosis in Ewing Family Tumors Gabriella Gamberi, Stefania Cocchi, Stefania Benini, Giovanna Magagnoli, Luca Morandi, Jennifer Kreshak, Marco Gambarotti, Piero Picci, Licciana Zanella, Marco Alberghini  The Journal of Molecular Diagnostics  Volume 13, Issue 3, Pages 313-324 (May 2011) DOI: 10.1016/j.jmoldx.2011.01.004 Copyright © 2011 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

Figure 1 Algorithm showing the protocol used in our laboratory to evaluate the presence of gene rearrangements in tumors with presumptive diagnosis of EFT. FISH, fluorescence in situ hybridization; LSI, locus-specific identifier (probe); FFPET, formalin-fixed paraffin-embedded tissue. The Journal of Molecular Diagnostics 2011 13, 313-324DOI: (10.1016/j.jmoldx.2011.01.004) Copyright © 2011 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

Figure 2 RT-PCR for detection of EWSR1-FLI1 transcript (A) and EWSR1-ERG transcript (B) in the same patient. Lane pt1 is the RT-PCR product obtained from patient's tumor RNA. In A, the band corresponds to a type 2 EWSR1-FLI1 fusion transcript; in B, no band is present, denoting a negative result for the EWSR1-ERG fusion. Lane C is the t(11;22) positive control; the band represents type 1 fusion. Lanes marked neg are negative controls, and the size marker (lane L) is a 100-bp DNA ladder (Promega). The Journal of Molecular Diagnostics 2011 13, 313-324DOI: (10.1016/j.jmoldx.2011.01.004) Copyright © 2011 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

Figure 3 Sequence analysis of an EWSR1-FLI1 fusion transcript at the breakpoint region, confirming the fusion of EWSR1 exon 10 to FLI1 exon 5 resulting in t(11;22) type 4. The Journal of Molecular Diagnostics 2011 13, 313-324DOI: (10.1016/j.jmoldx.2011.01.004) Copyright © 2011 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

Figure 4 A: Negative FISH analysis of FUS showing two normal fusion signals. B: Positive FISH analysis of EWSR1 for the same patient; arrows indicate the normal fusion signal and split red and green signals, indicating a rearrangement of one copy of the EWSR1 region. The Journal of Molecular Diagnostics 2011 13, 313-324DOI: (10.1016/j.jmoldx.2011.01.004) Copyright © 2011 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

Figure 5 The most prevalent types of exon breakpoints (indicated by boxed numbers) for the t(11;22) EWSR1-FLI1 translocation in EFT, with the number of positive cases identified in our series and the expected band size of the products, using primer pair EWS 22ex7-FLI1 11ex9. The Journal of Molecular Diagnostics 2011 13, 313-324DOI: (10.1016/j.jmoldx.2011.01.004) Copyright © 2011 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

Figure 6 The most prevalent types of exon breakpoints (indicated by boxed numbers) for the t(21;22) EWSR1-ERG translocation in EFT, with the number of positive cases identified in our series and the expected band size of the products, using primer pair EWSB-ERGB. The Journal of Molecular Diagnostics 2011 13, 313-324DOI: (10.1016/j.jmoldx.2011.01.004) Copyright © 2011 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

Figure 7 The most prevalent types of exon breakpoints (indicated by boxed numbers) for the rare translocations of EFT, with the expected band size of the products, using primer pair EWS 22ex7-FEV 2ex3. In the present study, we detected 1 case with t(2;22) EWSR1-FEV translocation. Translocations t(7;22), t(17;22), and t(20;22) are not yet routinely assessed in our laboratory. The Journal of Molecular Diagnostics 2011 13, 313-324DOI: (10.1016/j.jmoldx.2011.01.004) Copyright © 2011 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

Figure 8 The types of exon breakpoints (indicated by boxed numbers) of the rare variants in which the gene FUS is involved. The translocations t(2;16) and t(16;21) are not yet routinely assessed in our laboratory. The Journal of Molecular Diagnostics 2011 13, 313-324DOI: (10.1016/j.jmoldx.2011.01.004) Copyright © 2011 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

Figure 9 Schematic of results. EFT, Ewing sarcoma family tumors; FISH, fluorescence in situ hybridization; SRCT, small round-cell tumors; +, positive results; −, negative results. The Journal of Molecular Diagnostics 2011 13, 313-324DOI: (10.1016/j.jmoldx.2011.01.004) Copyright © 2011 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions