TY - JOUR
T1 - Basement membrane stiffness determines metastases formation
AU - Reuten, Raphael
AU - Zendehroud, Sina
AU - Nicolau, Monica
AU - Fleischhauer, Lutz
AU - Laitala, Anu
AU - Kiderlen, Stefanie
AU - Nikodemus, Denise
AU - Wullkopf, Lena
AU - Nielsen, Sebastian Rune
AU - McNeilly, Sarah
AU - Prein, Carina
AU - Rafaeva, Maria
AU - Schoof, Erwin M.
AU - Furtwängler, Benjamin
AU - Porse, Bo T.
AU - Kim, Hyobin
AU - Won, Kyoung Jae
AU - Sudhop, Stefanie
AU - Zornhagen, Kamilla Westarp
AU - Suhr, Frank
AU - Maniati, Eleni
AU - Pearce, Oliver M.T.
AU - Koch, Manuel
AU - Oddershede, Lene Broeng
AU - Van Agtmael, Tom
AU - Madsen, Chris D.
AU - Mayorca-Guiliani, Alejandro E.
AU - Bloch, Wilhelm
AU - Netz, Roland R.
AU - Clausen-Schaumann, Hauke
AU - Erler, Janine T.
PY - 2021
Y1 - 2021
N2 - 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.
AB - 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.
U2 - 10.1038/s41563-020-00894-0
DO - 10.1038/s41563-020-00894-0
M3 - Journal article
C2 - 33495631
SN - 1476-1122
VL - 20
SP - 892
EP - 903
JO - Nature Materials
JF - Nature Materials
ER -