BCR-ABL1 gene rearrangement as a subclonal change in ETV6-RUNX1–positive B-cell acute lymphoblastic leukemia by Karen A. Dun, Rob Vanhaeften, Tracey J.

Slides:



Advertisements
Similar presentations
NYU SCHOOL OF MEDICINE CYTOGENETICS LECTURE 2
Advertisements

Stem cell concepts renew cancer research by John E. Dick Blood Volume 112(13): December 15, 2008 ©2008 by American Society of Hematology.
Investigating a New Methodology for the Detection of Low Frequency 17p Deleted Clones in Chronic Lymphocytic Leukaemia (CLL): Impact on Prognostic Outcome.
A partial nontandem duplication of the MLL gene in four patients with acute myeloid leukemia  Iveta Šárová, Jana Březinová, Zuzana Zemanová, Libuše Lizcová,
Cytogenetic and molecular events in adenoma and well-differentiated thyroid follicular- cell neoplasia  Paola Caria, Roberta Vanni  Cancer Genetics and.
Figure 1. Microscopic findings and karyotyping
Standard and variant Philadelphia translocation in a CML patient with different sensitivity to imatinib therapy  Stefania Aliano, Gabriella Cirmena, Giuseppina.
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.
by Manuella L. Gomes Ochtrop, Sigune Goldacker, Annette M
How I treat LGL leukemia
EHT, a New Member of the MTG8/ETO Gene Family, Maps on 20q11 Region and Is Deleted in Acute Myeloid Leukemias by Nicola Stefano Fracchiolla, Gualtiero.
HS 4160 Critical Scientific Analysis
Volume 52, Issue 1, Pages (July 2007)
High EVI1 levels predict adverse outcome in acute myeloid leukemia: prevalence of EVI1 overexpression and chromosome 3q26 abnormalities underestimated.
Flow cytometric immunophenotyping for hematologic neoplasms
Misleading acute promyelocytic leukemia morphology
Clonal origins of relapse in ETV6-RUNX1 acute lymphoblastic leukemia
by Udomsak Bunworasate, Hilal Arnouk, Hans Minderman, Kieran L
Fluorescence in situ hybridization confirms the presence of Merkel cell polyomavirus in chronic lymphocytic leukemia cells by Anke Maria Haugg, Ernst-Jan.
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.
Cyclin D1-negative mantle cell lymphoma with cryptic t(12;14)(p13;q32) and cyclin D2 overexpression by Christian Herens, Frédéric Lambert, Leticia Quintanilla-Martinez,
Late relapses evolve from slow-responding subclones in t(12;21)-positive acute lymphoblastic leukemia: evidence for the persistence of a preleukemic clone.
by Rafael Fonseca, Richard J. Bailey, Gregory J. Ahmann, S
Expression of the chemokine receptors CXCR4, CXCR5, and CCR7 in primary central nervous system lymphoma by Kristoph Jahnke, Sarah E. Coupland, Il-Kang.
How I treat extramedullary acute myeloid leukemia
Acute myeloid leukemia is associated with retroviral gene transfer to hematopoietic progenitor cells in a rhesus macaque by Ruth Seggewiss, Stefania Pittaluga,
Fusion genes in cord blood
A20 (TNFAIP3) genetic alterations in EBV-associated AIDS-related lymphoma by Lisa Giulino, Susan Mathew, Gianna Ballon, Amy Chadburn, Sharon Barouk, Giuseppina.
MLL leukemia induction by t(9;11) chromosomal translocation in human hematopoietic stem cells using genome editing by Corina Schneidawind, Johan Jeong,
Detection of Trisomy 12 and Rb-Deletion in CD34+ Cells of Patients With B-Cell Chronic Lymphocytic Leukemia by B. Gahn, C. Schäfer, J. Neef, C. Troff,
The genetic basis of myelodysplasia and its clinical relevance
Fas-mediated apoptosis is important in regulating cell replication and death in trisomy 8 hematopoietic cells but not in cells with other cytogenetic abnormalities.
by Douglas D. Ross, Judith E. Karp, Tar T. Chen, and L. Austin Doyle
Jennelle C. Hodge, Patrick P. Bedroske, Kathryn E. Pearce, William R
Granulocyte colony-stimulating factor receptor mutations in a patient with acute lymphoblastic leukemia secondary to severe congenital neutropenia by Manuela.
by Giridharan Ramsingh, Meagan A. Jacoby, Jin Shao, Rigoberto E
FISH Analysis of Crizotinib Target Genes ROS1/ALK/MET in Malignant Mesothelioma  Sandra Salvi, PhD, Serena Varesano, PhD, Simona Boccardo, PhD, Jean Louis.
Fluorescence in Situ Hybridization Analysis of Immunoglobulin Heavy Chain Translocations in Plasma Cell Myeloma Using Intact Paraffin Sections and Simultaneous.
Loss of Heterozygosity and Microsatellite Instability at theMLL Locus Are Common in Childhood Acute Leukemia, but not in Infant Acute Leukemia by Julie.
Fluorescence In Situ Hybridization
Final Report Of Single-Center Study Of Chemotherapy Plus Dasatinib For The Initial Treatment Of Patients With Philadelphia-Chromosome Positive Acute Lymphoblastic.
TBL1XR1/TP63: a novel recurrent gene fusion in B-cell non-Hodgkin lymphoma by David W. Scott, Karen L. Mungall, Susana Ben-Neriah, Sanja Rogic, Ryan D.
by John Anastasi, Rizwan Moinuddin, and Christopher Daugherty
Identification of Combinatorial Genomic Abnormalities Associated with Prostate Cancer Early Recurrence  Xiaoyu Qu, Claudio Jeldres, Lena Glaskova, Cynthia.
Immunotherapy for acute lymphoblastic leukemia: from famine to feast
ALK and NRG1 Fusions Coexist in a Patient with Signet Ring Cell Lung Adenocarcinoma  Lucia Anna Muscarella, PhD, Domenico Trombetta, PhD, Federico Pio.
Evolution of a chemosensitive core-binding factor AML into an aggressive leukemia with eosinophilic differentiation by Wenbin Xiao, Mariko Yabe, Michael.
Daynna J. Wolff, Adam Bagg, Linda D. Cooley, Gordon W. Dewald, Betsy A
Advanced forms of MPNs are accompanied by chromosomal abnormalities that lead to dysregulation of TP53 by Bridget K. Marcellino, Ronald Hoffman, Joseph.
Successful Application of a Direct Detection Slide-Based Sequential Phenotype/Genotype Assay Using Archived Bone Marrow Smears and Paraffin Embedded.
Array Comparative Genomic Hybridization Detects Chromosomal Abnormalities in Hematological Cancers That Are Not Detected by Conventional Cytogenetics 
The Detection of t(14;18) in Archival Lymph Nodes
by Geling Li, Emily Waite, and Julie Wolfson
MYC DNA is structurally abnormal and MYC protein is overexpressed in MCL cells. MYC DNA is structurally abnormal and MYC protein is overexpressed in MCL.
A case of acute myeloid leukemia with promyelocytic features characterized by expression of a novel RARG-CPSF6 fusion by Christopher A. Miller, Christopher.
Quantitative proteomics of plasma vesicles identify novel biomarkers for hemoglobin E/β-thalassemic patients by Janejira Kittivorapart, Vanja Karamatic.
Jie Hu, Malini Sathanoori, Sally J. Kochmar, Urvashi Surti 
Heterogeneous leukemia stem cells in myeloid blast phase chronic myeloid leukemia by Ross Kinstrie, Dimitris Karamitros, Nicolas Goardon, Heather Morrison,
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,
Health outcomes and services in children with sickle cell trait, sickle cell anemia, and normal hemoglobin by Sarah L. Reeves, Hannah K. Jary, Jennifer.
A case of lenalidomide-dependent myelodysplastic syndrome
MtDNA analysis identifies 8 patients with PS in a cohort of DBA patients. mtDNA analysis identifies 8 patients with PS in a cohort of DBA patients. (A)
Acute Megakaryocytic Leukemia
Resistance mechanism for ibrutinib in marginal zone lymphoma
Primary Cutaneous CD30-Positive T-Cell Lymphoproliferative Disorders with Biallelic Rearrangements of DUSP22  Courtney R. Csikesz, Ryan A. Knudson, Patricia.
by Deogratias Ruhangaza, Andrew G. Evans, and Elizabeth A. Morgan
Bone marrow fibrosis associated with long-term imatinib therapy: resolution after switching to a second-generation TKI by Naranie Shanmuganathan, Susan.
ALK Gene Rearrangements: A New Therapeutic Target in a Molecularly Defined Subset of Non-small Cell Lung Cancer  Benjamin Solomon, MBBS, PhD, Marileila.
Myeloid neoplasms with eosinophilia
CD36 expression in tissue adjacent and distal to the tumor.
Presentation transcript:

BCR-ABL1 gene rearrangement as a subclonal change in ETV6-RUNX1–positive B-cell acute lymphoblastic leukemia by Karen A. Dun, Rob Vanhaeften, Tracey J. Batt, Louise A. Riley, Giuseppe Diano, and Jan Williamson BloodAdv Volume 1(2):132-138 December 13, 2016 © 2016 by The American Society of Hematology

Karen A. Dun et al. Blood Adv 2016;1:132-138 © 2016 by The American Society of Hematology

Patient’s bone marrow aspirate smear using May-Grünwald Giemsa stain. Patient’s bone marrow aspirate smear using May-Grünwald Giemsa stain. Image captured using Olympus microscope and camera. Original magnification ×200. Karen A. Dun et al. Blood Adv 2016;1:132-138 © 2016 by The American Society of Hematology

Conventional karyotype showing deletion of 6q, 11q, and trisomy of chromosome 21. Conventional karyotype showing deletion of 6q, 11q, and trisomy of chromosome 21. The conventional karyotype according to the International Society of Cytogenetic Nomenclature 2013 was 47,XX,del(6)(q22),del(11)(q13q23),+21[10]/46,XX[10]. Image captured using Zeiss microscope and MetaSystems image analysis software. Karen A. Dun et al. Blood Adv 2016;1:132-138 © 2016 by The American Society of Hematology

FISH images of sequential hybridization with the Vysis ETV6 break-apart probe and the MetaSystems BCR-ABL1 dual-fusion probe. FISH images of sequential hybridization with the Vysis ETV6 break-apart probe and the MetaSystems BCR-ABL1 dual-fusion probe. The left-hand images (A,C) show the first hybridization with the ETV6 probe. The signal pattern shows 1 normal ETV6 signal and separated 3 ′ETV6 and 5 ′ETV6 signals, indicating the ETV6 gene rearrangement (t(12;21)(p13;q22)). The right-hand images (B,D) show the same cells sequentially hybridized with the BCR-ABL1 probe. The signal pattern shows 2 copies of ABL1, 1 copy of BCR, and 1 BCR-ABL1 fusion signal consistent with the BCR-ABL1 gene rearrangement, as demonstrated by molecular techniques. Image captured using Zeiss microscope and MetaSystems image analysis software. Karen A. Dun et al. Blood Adv 2016;1:132-138 © 2016 by The American Society of Hematology