Genes and proteins of myeloma endothelial cells to search specific targets of the tumor vasculature

Domenico Ribatti, Angelo Vacca

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Multiple myeloma (MM) mainly progresses in the bone marrow (BM). Therefore signals from BM microenvironment are thought to play a critical role in maintaining plasma cell growth, migration, and survival. Reciprocal positive and negative interactions between plasma cells and BM stromal cells, namely endothelial cells (ECs), ECs progenitor cells, hematopoietic stem cells, osteoblasts/osteoclasts, chondroclasts, fibroblasts, macrophages, and mast cells, are mediated by an array of cytokines, receptors, and adhesion molecules. BM neovascularization is a constant hallmark of MM, and goes hand in hand with progression until leukemic phase. MM neovessels form through angiogenesis and vasculogenesis, and are endowed with the overangiogenic phenotype of ECs (MMECs). Induction of the vascular phase in MM is sustained by angiogenic cytokines, such as vascular endothelial growth factor (VEGF), basic fi broblast growth factor (bFGF), hepatocyte growth factor (HGF), platelet derived growth factor (PDGF) and metalloproteinases, secreted by the BM plasma cells, and overexpressed in MMECs. BM microenvironmental factors induce MMECs to become functionally different from MGUS ECs (MGECs), i.e., to be characterized by an overangiogenic phenotype, and be similar to transformed cells. In fact, MMECs down- or up-regulate some genes like tumor cells. The induced phenotypic and genotypic modi fi cations of MMECs entail at least 22 different genes that are ivolved in specific pathways which control apoptosis, extracellular matrix formation and bone remodeling, cell adhesion, angiogenesis, and cell proliferation. These alterations play an important role in MM progression and may represent new molecular markers for prognostic stratification of patients and prediction of the response to antiangiogenic drugs as well as new potential therapeutic targets.

Original languageEnglish
Title of host publicationAdvances in Biology and Therapy of Multiple Myeloma: Volume 1: Basic Science
PublisherSpringer New York
Pages241-254
Number of pages14
ISBN (Print)9781461446668, 9781461446651
DOIs
Publication statusPublished - Jan 1 2013

ASJC Scopus subject areas

  • Medicine(all)

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  • Cite this

    Ribatti, D., & Vacca, A. (2013). Genes and proteins of myeloma endothelial cells to search specific targets of the tumor vasculature. In Advances in Biology and Therapy of Multiple Myeloma: Volume 1: Basic Science (pp. 241-254). Springer New York. https://doi.org/10.1007/978-1-4614-4666-8_13