[HTML][HTML] The matricellular receptor LRP1 forms an interface for signaling and endocytosis in modulation of the extracellular tumor environment

B Van Gool, S Dedieu, H Emonard… - Frontiers in …, 2015 - frontiersin.org
B Van Gool, S Dedieu, H Emonard, AJM Roebroek
Frontiers in pharmacology, 2015frontiersin.org
The membrane protein low-density lipoprotein receptor related-protein 1 (LRP1) has been
attributed a role in cancer. However, its presumably often indirect involvement is far from
understood. LRP1 has both endocytic and signaling activities. As a matricellular receptor it is
involved in regulation, mostly by clearing, of various extracellular matrix degrading enzymes
including matrix metalloproteinases, serine proteases, protease inhibitor complexes, and the
endoglycosidase heparanase. Furthermore, by binding extracellular ligands including …
The membrane protein low-density lipoprotein receptor related-protein 1 (LRP1) has been attributed a role in cancer. However, its presumably often indirect involvement is far from understood. LRP1 has both endocytic and signaling activities. As a matricellular receptor it is involved in regulation, mostly by clearing, of various extracellular matrix degrading enzymes including matrix metalloproteinases, serine proteases, protease inhibitor complexes, and the endoglycosidase heparanase. Furthermore, by binding extracellular ligands including growth factors and subsequent intracellular interaction with scaffolding and adaptor proteins it is involved in regulation of various signaling cascades. LRP1 expression levels are often downregulated in cancer and some studies consider low LRP1 levels a poor prognostic factor. On the contrary, upregulation in brain cancers has been noted and clinical trials explore the use of LRP1 as cargo receptor to deliver cytotoxic agents. This mini-review focuses on LRP1’s role in tumor growth and metastasis especially by modulation of the extracellular tumor environment. In relation to this role its diagnostic, prognostic and therapeutic potential will be discussed.
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