Gene expression profiling reveals a close relationship between follicular lymphoma grade 3A and 3B, but distinct profiles of follicular lymphoma grade 1 and 2
Autor: | Rainer Spang, Markus Kreuz, Ellen Leich, Lorenz Trümper, Heike Horn, Andreas Rosenwald, German Ott, Michael Hummel, Markus Loeffler, Christian W. Kohler, Raphael Witzig, Wolfram Klapper |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
Adult
Male Non-Hodgkin Lymphoma Follicular lymphoma Biology Article 03 medical and health sciences 0302 clinical medicine immune system diseases hemic and lymphatic diseases Gene expression medicine Biomarkers Tumor Humans Lymphoma Follicular Genetic Association Studies In Situ Hybridization Fluorescence Aged Regulation of gene expression medicine.diagnostic_test Gene Expression Profiling Germinal center Computational Biology Hematology Middle Aged BCL6 medicine.disease Immunohistochemistry Lymphoma Gene expression profiling Gene Expression Regulation Neoplastic 030220 oncology & carcinogenesis Cancer research Female Neoplasm Grading Transcriptome 030215 immunology Fluorescence in situ hybridization |
Zdroj: | Haematologica |
ISSN: | 1592-8721 0390-6078 |
Popis: | A linear progression model of follicular lymphomas (FL) FL1, FL2 and FL3A has been favored, since FL3A often co-exist with an FL1/2 component. FL3B, in contrast, is thought to be more closely related to diffuse large B-cell lymphoma (DLBCL), and both are often simultaneously present in one tumor (DLBCL/FL3B). To obtain more detailed insights into follicular lymphoma progression, a comprehensive analysis of a well-defined set of FL1/2 (n=22), FL3A (n=16), FL3B (n=6), DLBCL/FL3B (n=9), and germinal center B-cell-type diffuse large B-cell lymphoma (n=45) was undertaken using gene expression profiling, immunohistochemical stainings and genetic analyses by fluorescence in situ hybridization. While immunohistochemical (CD10, IRF4/MUM1, Ki67, BCL2, BCL6) and genetic profiles (translocations of BCL2, BCL6 and MYC) delineate FL1-3A from FL3B and DLBCL/FL3B, significant differences were observed between FL1/2 and FL3A upon gene expression profiling. Interestingly, FL3B turned out to be closely related to FL3A, not categorizing within a separate gene expression cluster, and both FL3A and FL3B showed overlapping profiles in between FL1/2 and diffuse large B-cell lymphoma. Finally, based upon their gene expression pattern, DLBCL/FL3B represent a composite form of FL3B and DLBCL, with the majority of samples more closely resembling the latter. The fact that gene expression profiling clearly separated FL1/2 from both FL3A and FL3B suggests a closer biological relationship between the latter. This notion, however, is in contrast to immunohistochemical and genetic profiles of the different histological FL subtypes that point to a closer relationship between FL1/2 and FL3A, and separates them from FL3B. |
Databáze: | OpenAIRE |
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