| Literature DB >> 27873269 |
Abstract
The 3D nuclear architecture is closely related to cellular functions and chromosomes are organized in distinct territories. Quantitative 3D telomere FISH analysis (3D Q-FISH) and 3D super-resolution imaging (3D-SIM) at a resolution up to 80 nm as well as the recently developed combined quantitative 3D TRF2-telomere immune FISH technique (3D TRF2/Telo-Q-FISH) have substantially contributed to elucidate molecular pathogenic mechanisms of hematological diseases. Here we report the methods we applied to uncover major molecular steps involved in the pathogenesis of EBV-associated Hodgkin's lymphoma. These methods allowed us to identify the EBV-encoded oncoprotein LMP1 as a key element in the formation of Hodgkin (H-cell) and multinucleated Reed-Sternberg cells (RS-cell), the diagnostic tumor cell of classical Hodgkin's lymphoma (cHL). LMP1 mediates multinuclearity through downregulation of shelterin proteins, in particular telomere repeat binding factor 2 (TRF2).Entities:
Keywords: 3D Q-FISH; 3D TRF2/Telo-Q-FISH; Hodgkin cell; Hodgkin’s lymphoma; LMP1 oncoprotein; Reed-Sternberg cell; Shelterin; TRF2; Telomere; Three-dimensional (3D) imaging
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Year: 2017 PMID: 27873269 DOI: 10.1007/978-1-4939-6655-4_6
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745