Descripción de un caso de leucemia mieloide crónica con un cromosoma Philadelphia variante

Contenido principal del artículo

Leandro G. Gutiérrez
Patricia D. Dos Santos
Amada Rolón
Ana M. Melnichuk
Carina F. Argüelles
Alberto S. Fenocchio

Resumen

En 5–10% de los casos de Leucemia Mieloide Crónica (LMC), el cromosoma Philadelphia (Ph1) se origina como producto de translocaciones variantes (Ph1 variante). Estas últimas involucran otros autosomas además del 9 y 22 clásicamente implicados. Se presenta aquí un caso de LMC cuyo cromosoma Ph1 variante fue originado a partir de una translocación compleja que involucró los cromosomas 3, 9 y 22 [t(3;9;22)(p21,q34;q11)]. El análisis mediante FISH sugiere un mecanismo de formación en una etapa única, mientras el análisis por RT-PCR mostró la presencia del rearreglo molecular BCR/ABL1 correspondiente a la isoforma p210. El paciente no presentó variaciones significativas en los parámetros de respuesta clínica (respuesta hematológica, respuesta citogenética y respuesta molecular) respecto de aquellos pacientes con el Ph1 estándar.

Descargas

Los datos de descargas todavía no están disponibles.

Detalles del artículo

Cómo citar
Gutiérrez, L. G., Dos Santos, P. D., Rolón, A., Melnichuk, A. M., Argüelles, C. F., & Fenocchio, A. S. (2017). Descripción de un caso de leucemia mieloide crónica con un cromosoma Philadelphia variante. Revista De Ciencia Y Tecnología, 27(1), 46–50. Recuperado a partir de https://www.fceqyn.unam.edu.ar/recyt/index.php/recyt/article/view/327
Sección
Biología y Genética

Citas

Kantarjian H, Talpaz M, Giles F, [et al]. New insights into the pathophysiology of chronic myeloid leukemia and imatinib resistance. Annals of Internal Medicine 19; 145: 913–923. 2006.

Kurzrock R, Kantarjian HM, Druker BJ, [et al]. Philadelphia Chromosome-Positive Leukemias: From Basic Mechanisms to Molecular Therapeutics. Annals International Medicine 10, 138: 819–830. 2003.

Nowell PC & Hungerford DA. A minute chromosome in human chronic granulocytic leukemia. Science, 132: 1497. 1960.

Rowley JD. A new consistent chromosomal abnormality in chronic myelogenous leukemia. Nature 243: 290–293. 1973.

Rowley JD. The critical role of chromosome translocations in human leukemias. Annual Review of Genetics 32: 495–519. 1998.

Fröling S & Dohner H. Chromosomal abnormalities in cancer. The New England Journal of Medicine 359: 722-34. 2008.

Goldman J. & Melo J. Chronic myeloid leukemia-advances in biology and new approaches to treatment. The New England Journal of Medicine 349: 1451–1464. 2003.

Melo JV, Hughes TP & Apperley JF. Chronic myeloid leukemia Hematology/American Society of Hematology 1: 132–137. 2003.

Heim S & Mitelman F. Cancer cytogenetics, 3rd Edition. Hoboken, New Jersey, Wiley Blackwell, a John Wiley & Sons, Inc., publication. Cap 7, p179–207. 2009

Gallego S, Baialardo E, Gutiérrrez M, [et al]. A new variant Ph translocation in chronic myeloid leukemia: t(Y;22)(p11;q11). Cancer Genetics and Cytogenetics 87: 75–78.1996

Naumann S & Decker H. Genesis of variant Philadelphia chromosome translocations in chronic myelocytic leukemia. Cancer Genetics and Cytogenetics, 147: 18–22. 2003.

Fisher AM, Strike P, Scott C, [et al]. Breakpoints of variant 9;22 translocations in chronic myeloid leukemia locate preferentially in the CG-richest regions of the genome. Genes Chromosomes & Cancer 43: 383–389. 2005.

Bennour A, Sennana H, Laatiri A, [et al]. Molecular cytogentic characterization of variant Philadelphia translocations in chronic myeloid leukemia: genesis and deletion of derivative chromosome 9. Cancer Genetics and Cytogenetics 194: 30–37. 2009.

Richerbourg S, Eclache V, Perot C, [et al]. Mechanisms of genesis of variant translocation in chronic myeloid leukemia are not correlated with ABL1 or BCR deletion status or response to imatinib therapy. Cancer Genetics and Cytogenetics 182: 95–102. 2008.

Gorusu M, Benn P, Li Z [et al]. On the genesis and prognosis of variant translocations in chronic myeloid leukemia. Cancer Genetics and Cytogenetics, 173: 97–106. 2007.

Belli C, Alú MF, Alfonso G, [et al]. Novel variant Ph translocation t(9;22;11)(q34;q11.2;p15)inv(9)(p13q34) in chronic myeloid leukemia involving a one-step mechanism. Cytogenetic and Genome Research 132, 4: 304–308. 2011.

Reid AG, Huntly BJ, Grace C, [et al]. Survival implications of molecular heterogeneity in variant Philadelphia-positive chronic myeloid leukaemia. British Journal of Haematology 121: 419–427. 2003.

Yehuda O, Abeliovich D, Ben-Neriah S, [et al]. Clinical implications of fluorescence in situ hybridization analysis in 13 chronic myeloid leukemia cases: Ph negative and variant Ph-positive. Cancer Genetics and Cytogenetics, 114:100–107. 1999.

Reddy KS & Sulcova V. A FISH study of variant Philadelphia rearrangements. Cancer Genetics and Cytogenetics, 118:121–131. 2000.

Loncarevic IF, Romer J, Starke H, [et al]. Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemia. Genes Chromosomes & Cancer 34: 193–200. 2002.

Shaffer L, Slovak M & Campbell L editors. International Standing Committee on Human Cytogenetic Nomenclature. An International System for Human Cytogenetic Nomenclature. Cytogenetic and Genome Research. 2009.

Cross N. Detection of BCR-ABL in Hematological Malignancies by RT-PCR. Cotter F.E. Molecular Diagnosis of Cancer. Cap 2, p 25–36. 1996.

Mitelman Database of Chromosome Aberrations in Cancer. (2013). Mitelman F, Johansson B & Mertens F. Available at http://cgap.nci.nih.gov/Chromosomes/Mitelman. (verificado: Sep 2015).

Barbata G, Granata G, Bellanca F, [et al]. Complex trasnlocation t(3;9;22) and paracentric inversion of chromosome 3 in blastic crisis of chronic myeloid leukemia. Cancer Genetic and Cytogenetic 20: 305–309. 1986.

Albano F, Anelli L, Zagaria A, [et al]. Non-random distribution of genomic features in breakpoint regions involved in chronic myeloid leukemia cases with variant t(9;22) or additional chromosomal rearrangements. Molecular Cancer, 9:120. 2010.

Bennour A, Bellâaj H, Youssef B, [et al], Molecular cytogenetic characterization of Philadelphia-negative rearrangements in chronic myeloid leukemia patients. Journal of Cancer Research and Clinical Oncology 137:1329–1336. 2011.

Buda G, Orciulo E, Maggini V, [et al]. Complex translocation t(3;9;22)(p21;q34;q11) at diagnosis is a negative prognostic index in chronic myeloid leukemia. Leukemia research, 32: 192–194. 2008.

Tan J, Cang S, Seiter K, [et al]. t(3;9;22) 3-Way chromosome translocation in chronic myeloid leukemia is associated with poor prognosis. Cancer Investigation, 27:718–722. 2009.

Gutiérrez LG, Belli C, Ferri C, [et al]. Clonal Evolution and Cytogenetic Changes in Chronic Myeloid Leukemia. Urbano K., NOVA Publisher group: Advances in genetics Research. Vol. 11, Cap 8, p 181–200. 2014. Available at https://www.novapublishers.com/catalog/product_info.php?products_id=47854 (verificado Sep 2015).

Specchia G, Albano F, Anelli L, [et al]. Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes. Leukemia & Lymphoma 45, 4: 689–694. 2004.

Druker B, Talpaz M, Resta D, [et al]. Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. The New England Journal of Medicine 344-a: 1031–1037, 2001.

Druker B, Sawyers C, Kantarjian H, [et al]. Activity of a specific inhibitor of the BCR-ABL tyrosine kinase in the blast crisis of chronic myeloid leukemia and acute lymphoblastic leukemia with the Philadelphia chromosome. The New England Journal of Medicine 344-b: 1038–1042, 2001.

Baccarani M, Cortes J, Pane F, [et al]. Chronic myeloid leukemia: an update of concepts and management recommendations of European LeukemiaNet. Journal of Clinical Oncology, 27: 6041–6051. 2009.

Batty N, Kantarjian H, Borthakur G, [et al]. Patients with chronic myeloid leukemia with variant Philadelphia chromosome (Ph) translocations have a similar outcome as those with classic Ph when treated with imatinib or 2nd generation TKI. Blood 112: 1108. 2008.

Marzocchi G, Castagnetti F, Luatti S, [et al]. Variant Philadelphia translocations: molecular-cytogenetic characterization and prognostic influence on frontline imatinib therapy, a GIMEMA Working Party on CML analysis. Blood, 117: 6793–6800. 2011.

Baccarani M, Deininger MW, Rosti G, [et al]. European LeukemiaNet recommendations for the management of chronic myeloid leukemia. Blood, 122: 872-884. 2013.

Koshiyama DB, Capra ME, Paskulin G, [et al]. Cytogenetic response to imatinib treatment in Southern Brazilian patients with chronic myelogenous leukemia and variant Philadelphia chromosome. Ann Hematol 92:185–189. 2013.

Beligoy L, Bengio R, Bordone J, [et al]. Guías de tratamiento: Leucemia Mieloide Crónica. Sociedad Argentina de Hematología. Editora: Silvina Palmer. Tomo II: 503. Available at http://www.sah.org.ar/guias_hematolo.asp. (verificado Sep 2015).

Contador de visualizaciones: Resumen : 76 vistas.