4.4 Article

Tumor Heterogeneity in Lymphomas: A Different Breed

期刊

PATHOBIOLOGY
卷 85, 期 1-2, 页码 130-145

出版社

KARGER
DOI: 10.1159/000475530

关键词

Chronic lymphocytic leukemia/small lymphocytic lymphoma; Clonal evolution; Diffuse large B-cell lymphoma; Follicular lymphoma; Intratumoral heterogeneity; Lymphoma; Lymphoplasmacytic lymphoma; Mantle cell lymphoma; B-cell non-Hodgkin lymphoma; Tumor heterogeneity

资金

  1. Clinical Medicine Plus Scholarship from the Prof. Dr. Max Cloetta Foundation
  2. Uniscientia Foundation Vaduz
  3. TUFF program of the University of Tubingen [2320-0-0]

向作者/读者索取更多资源

The facts that cancer represents tissues consisting of heterogeneous neoplastic, as well as reactive, cell populations and that cancers of the same histotype may show profound differences in clinical behavior have long been recognized. With the advent of new technologies and the demands of precision medicine, the investigation of tumor heterogeneity has gained much interest. An understanding of intertumoral heterogeneity in patients with the same disease entity is necessary to optimally guide personalized treatment. In addition, increasing evidence indicates that different tumor areas or primary tumors and metastases in an individual patient can show significant intratumoral heterogeneity on different levels. This phenomenon can be driven by genomic instability, epigenetic events, the tumor microenvironment, and stochastic variations in cellular function and antitumoral therapies. These mechanisms may lead to branched sub-clonal evolution from a common progenitor clone, resulting in spatial variation between different tumor sites, disease progression, and treatment resistance. This review addresses tumor heterogeneity in lymphomas from a pathologist's viewpoint. The relationship between morphologic, immunophenotypic, and genetic heterogeneity is exemplified in different lymphoma entities and reviewed in the context of high-grade transformation and transdifferentiation. In addition, factors driving heterogeneity, as well as clinical and therapeutic implications of lymphoma heterogeneity, will be discussed. (C) 2017 S. Karger AG, Basel

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