An Integrated Genomic Approach to the Assessment and Treatment of Acute Myeloid Leukemia

作者: Lucy A. Godley , John Cunningham , M. Eileen Dolan , R. Stephanie Huang , Sandeep Gurbuxani

DOI: 10.1053/J.SEMINONCOL.2011.01.003

关键词:

摘要: Traditionally, new scientific advances have been applied quickly to the leukemias based on ease with which relatively pure samples of malignant cells can be obtained. Currently, our arsenal approaches used characterize an individual's acute myeloid leukemia (AML) combines hematopathologic evaluation, flow cytometry, cytogenetic analysis, and molecular studies focused a few key genes. The advent high-throughput methods capable full-genome evaluation presents options for revolutionary change in way we diagnose, characterize, treat AML. Next-generation DNA sequencing techniques allow full cancer genome or transcriptome, hope that this will affordable routine clinical care within decade. Microarray-based testing define gene miRNA expression, methylation patterns, chromosomal imbalances, predisposition disease chemosensitivity. vision future entails integrated automated approach these analyses, bringing possibility formulating individualized treatment plan days patient's initial presentation. With expectations comes such lead decreased toxicities prolonged survival patients.

参考文章(77)
Richard A. Larson, Yunxia Wang, Mekhala Banerjee, Joseph Wiemels, Christine Hartford, Michelle M. Le Beau, Martyn T. Smith, Prevalence of the inactivating 609C-->T polymorphism in the NAD(P)H:quinone oxidoreductase (NQO1) gene in patients with primary and therapy-related myeloid leukemia. Blood. ,vol. 94, pp. 803- 807 ,(1999) , 10.1182/BLOOD.V94.2.803
CA Felix, MR Hosler, D Provisor, K Salhany, EA Sexsmith, DJ Slater, NK Cheung, NJ Winick, EA Strauss, R Heyn, BJ Lange, D Malkin, The p53 gene in pediatric therapy-related leukemia and myelodysplasia Blood. ,vol. 87, pp. 4376- 4381 ,(1996) , 10.1182/BLOOD.V87.10.4376.BLOODJOURNAL87104376
Jerald P. Radich, Andrew D. Zelenetz, Wing C. Chan, Carlo M. Croce, Myron S. Czuczman, Harry P. Erba, Sandra J. Horning, Jane Houldsworth, B. Douglas Smith, David S. Snyder, Hema M. Sundar, Meir Wetzler, Jane N. Winter, NCCN task force report: molecular markers in leukemias and lymphomas. Journal of The National Comprehensive Cancer Network. ,vol. 7, ,(2009) , 10.6004/JNCCN.2009.0077
L Bullinger, J Krönke, C Schön, I Radtke, K Urlbauer, U Botzenhardt, V Gaidzik, A Carió, C Senger, R F Schlenk, J R Downing, K Holzmann, K Döhner, H Döhner, Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis. Leukemia. ,vol. 24, pp. 438- 449 ,(2010) , 10.1038/LEU.2009.263
Guido Marcucci, Michael D. Radmacher, Kati Maharry, Krzysztof Mrózek, Amy S. Ruppert, Peter Paschka, Tamara Vukosavljevic, Susan P. Whitman, Claudia D. Baldus, Christian Langer, Chang-Gong Liu, Andrew J. Carroll, Bayard L. Powell, Ramiro Garzon, Carlo M. Croce, Jonathan E. Kolitz, Michael A. Caligiuri, Richard A. Larson, Clara D. Bloomfield, MicroRNA expression in cytogenetically normal acute myeloid leukemia The New England Journal of Medicine. ,vol. 358, pp. 1919- 1928 ,(2008) , 10.1056/NEJMOA074256
J. Suela, S. Alvarez, J.C. Cigudosa, DNA profiling by arrayCGH in acute myeloid leukemia and myelodysplastic syndromes Cytogenetic and Genome Research. ,vol. 118, pp. 304- 309 ,(2007) , 10.1159/000108314
C G Mathew, Fanconi anaemia genes and susceptibility to cancer Oncogene. ,vol. 25, pp. 5875- 5884 ,(2006) , 10.1038/SJ.ONC.1209878
Matthew J Walter, Timothy A Graubert, John F DiPersio, Elaine R Mardis, Richard K Wilson, Timothy J Ley, Next-generation sequencing of cancer genomes: back to the future Personalized Medicine. ,vol. 6, pp. 653- 653 ,(2009) , 10.2217/PME.09.52
G. L Bond, C. Menin, R. Bertorelle, P. Alhopuro, L. A Aaltonen, A. J Levine, MDM2 SNP309 Accelerates colorectal tumour formation in women Journal of Medical Genetics. ,vol. 43, pp. 950- 952 ,(2006) , 10.1136/JMG.2006.043539
Jane E. Churpek, Kenan Onel, Heritability of Hematologic Malignancies: From Pedigrees to Genomics Hematology-oncology Clinics of North America. ,vol. 24, pp. 939- 972 ,(2010) , 10.1016/J.HOC.2010.06.001