» Articles » PMID: 24930031

Extracellular Matrix Stiffness and Composition Jointly Regulate the Induction of Malignant Phenotypes in Mammary Epithelium

Overview
Journal Nat Mater
Date 2014 Jun 16
PMID 24930031
Citations 382
Authors
Affiliations
Soon will be listed here.
Abstract

In vitro models of normal mammary epithelium have correlated increased extracellular matrix (ECM) stiffness with malignant phenotypes. However, the role of increased stiffness in this transformation remains unclear because of difficulties in controlling ECM stiffness, composition and architecture independently. Here we demonstrate that interpenetrating networks of reconstituted basement membrane matrix and alginate can be used to modulate ECM stiffness independently of composition and architecture. We find that, in normal mammary epithelial cells, increasing ECM stiffness alone induces malignant phenotypes but that the effect is completely abrogated when accompanied by an increase in basement-membrane ligands. We also find that the combination of stiffness and composition is sensed through β4 integrin, Rac1, and the PI3K pathway, and suggest a mechanism in which an increase in ECM stiffness, without an increase in basement membrane ligands, prevents normal α6β4 integrin clustering into hemidesmosomes.

Citing Articles

tailored confining microenvironment for lung cancer spheroids.

Dong Y, Qian S, Wang X, Zhang W, Lu W, Qu J Mater Today Bio. 2025; 31:101602.

PMID: 40070872 PMC: 11894329. DOI: 10.1016/j.mtbio.2025.101602.


Three-Dimensional Models: Biomimetic Tools That Recapitulate Breast Tissue Architecture and Microenvironment to Study Ductal Carcinoma In Situ Transition to Invasive Ductal Breast Cancer.

Shah S, Osuala K, Brock E, Ji K, Sloane B, Mattingly R Cells. 2025; 14(3).

PMID: 39937011 PMC: 11817749. DOI: 10.3390/cells14030220.


Insights into the mechanisms, regulation, and therapeutic implications of extracellular matrix stiffness in cancer.

Zhang X, Al-Danakh A, Zhu X, Feng D, Yang L, Wu H Bioeng Transl Med. 2025; 10(1):e10698.

PMID: 39801760 PMC: 11711218. DOI: 10.1002/btm2.10698.


Type I collagen extracellular matrix facilitates nerve regeneration via the construction of a favourable microenvironment.

Lu P, Chen Z, Wu M, Feng S, Chen S, Cheng X Burns Trauma. 2024; 12:tkae049.

PMID: 39659559 PMC: 11631217. DOI: 10.1093/burnst/tkae049.


Forcing the code: tension modulates signaling to drive morphogenesis and malignancy.

Narain R, Muncie-Vasic J, Weaver V Genes Dev. 2024; 39(1-2):163-181.

PMID: 39638568 PMC: 11789492. DOI: 10.1101/gad.352110.124.


References
1.
Liu H, Radisky D, Wang F, Bissell M . Polarity and proliferation are controlled by distinct signaling pathways downstream of PI3-kinase in breast epithelial tumor cells. J Cell Biol. 2004; 164(4):603-12. PMC: 2171976. DOI: 10.1083/jcb.200306090. View

2.
Lee E, Lotz M, Steele Jr G, Mercurio A . The integrin alpha 6 beta 4 is a laminin receptor. J Cell Biol. 1992; 117(3):671-8. PMC: 2289449. DOI: 10.1083/jcb.117.3.671. View

3.
Yuan T, Cantley L . PI3K pathway alterations in cancer: variations on a theme. Oncogene. 2008; 27(41):5497-510. PMC: 3398461. DOI: 10.1038/onc.2008.245. View

4.
Ali S, Coombes R . Estrogen receptor alpha in human breast cancer: occurrence and significance. J Mammary Gland Biol Neoplasia. 2004; 5(3):271-81. DOI: 10.1023/a:1009594727358. View

5.
Lo C, Wang H, Dembo M, Wang Y . Cell movement is guided by the rigidity of the substrate. Biophys J. 2000; 79(1):144-52. PMC: 1300921. DOI: 10.1016/S0006-3495(00)76279-5. View