| Literature DB >> 33495631 |
Sina Zendehroud1, Monica Nicolau2, Raphael Reuten3, Lutz Fleischhauer4,5, Anu Laitala2, Stefanie Kiderlen4,5, Denise Nikodemus2, Lena Wullkopf2, Sebastian Rune Nielsen2, Sarah McNeilly6, Carina Prein4,5,7, Maria Rafaeva2, Erwin M Schoof2,8,9,10, Benjamin Furtwängler2,9,10, Bo T Porse2,9,10, Hyobin Kim2,10, Kyoung Jae Won2,10, Stefanie Sudhop5, Kamilla Westarp Zornhagen2, Frank Suhr11, Eleni Maniati12, Oliver M T Pearce12, Manuel Koch13,14, Lene Broeng Oddershede15, Tom Van Agtmael6, Chris D Madsen16, Alejandro E Mayorca-Guiliani2, Wilhelm Bloch17, Roland R Netz1, Hauke Clausen-Schaumann4,5, Janine T Erler18.
Abstract
The basement membrane (BM) is a special type of extracellular matrix and presents the major barrier cancer cells have to overcome multiple times to form metastases. Here we show that BM stiffness is a major determinant of metastases formation in several tissues and identify netrin-4 (Net4) as a key regulator of BM stiffness. Mechanistically, our biophysical and functional analyses in combination with mathematical simulations show that Net4 softens the mechanical properties of native BMs by opening laminin node complexes, decreasing cancer cell potential to transmigrate this barrier despite creating bigger pores. Our results therefore reveal that BM stiffness is dominant over pore size, and that the mechanical properties of 'normal' BMs determine metastases formation and patient survival independent of cancer-mediated alterations. Thus, identifying individual Net4 protein levels within native BMs in major metastatic organs may have the potential to define patient survival even before tumour formation. The ratio of Net4 to laminin molecules determines BM stiffness, such that the more Net4, the softer the BM, thereby decreasing cancer cell invasion activity.Entities:
Year: 2021 PMID: 33495631 DOI: 10.1038/s41563-020-00894-0
Source DB: PubMed Journal: Nat Mater ISSN: 1476-1122 Impact factor: 43.841