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Semin Diagn Pathol. 2002 May;19(2):72-93.

Molecular genetic methods in the diagnosis of hematologic neoplasms.

Author information

1
Department of Hematopathology, The University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.

Abstract

Leukemias and lymphomas are monoclonal neoplasms that arise as a result of molecular abnormalities. These abnormalites are diverse but can be grouped into two general categories, chromosomal translocations that usually result in oncogene activation and inactivation of tumor suppressor genes. Recent advances in our understanding of chromosomal translocations have led to improved classification of leukemias and lymphomas. For example, the t(9;22)(q34;q11) is now considered a defining feature of chronic myeloid leukemia, and the t(2;5)(p23;q35) defines a clinically and biologically unique subset of anaplastic large cell lymphomas. In this review, we focus on chromosomal translocations in hematologic neoplasms and the techniques used for their detection. We also briefly discuss tumor suppressor genes and assessment of clonality in lymphoid neoplasms.

PMID:
12036283
[Indexed for MEDLINE]

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