Cancer Metastasis: The Role of the Extracellular Matrix and the Heparan Sulfate Proteoglycan Perlecan

Cancer metastasis is the dissemination of tumor cells to new sites, resulting in the formation of secondary tumors. This process is complex and is spatially and temporally regulated by intrinsic and extrinsic factors. One important extrinsic factor is the extracellular matrix, the non-cellular compo...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in oncology Vol. 9; p. 1482
Main Authors Elgundi, Zehra, Papanicolaou, Michael, Major, Gretel, Cox, Thomas R, Melrose, James, Whitelock, John M, Farrugia, Brooke L
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 17.01.2020
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Cancer metastasis is the dissemination of tumor cells to new sites, resulting in the formation of secondary tumors. This process is complex and is spatially and temporally regulated by intrinsic and extrinsic factors. One important extrinsic factor is the extracellular matrix, the non-cellular component of tissues. Heparan sulfate proteoglycans (HSPGs) are constituents of the extracellular matrix, and through their heparan sulfate chains and protein core, modulate multiple events that occur during the metastatic cascade. This review will provide an overview of the role of the extracellular matrix in the events that occur during cancer metastasis, primarily focusing on perlecan. Perlecan, a basement membrane HSPG is a key component of the vascular extracellular matrix and is commonly associated with events that occur during the metastatic cascade. Its contradictory role in these events will be discussed and we will highlight the recent advances in cancer therapies that target HSPGs and their modifying enzymes.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
Reviewed by: Mary C. (Cindy) Farach-Carson, University of Texas Health Science Center at Houston, United States; Maurizio Mongiat, Centro di Riferimento Oncologico di Aviano (IRCCS), Italy
Edited by: Cinzia Lanzi, Fondazione IRCCS Istituto Nazionale dei Tumori, Italy
This article was submitted to Cancer Molecular Targets and Therapeutics, a section of the journal Frontiers in Oncology
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2019.01482