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Matrix hyaluronan alters epidermal growth factor receptor-dependent cell morphology.


ABSTRACT: EGFR, a critical regulator of oncogenic signaling during cancer progression, is capable of integrating multireceptor signaling pathways that promote metastasis. EGFR is subject to regulatory cues from the extracellular matrix (ECM), of which hyaluronan (HA) is a major component. In mammary tumors, HA is deposited in the ECM where it functions in biomechanical support and modulates intracellular signaling. We utilized a 3D collagen system in which HA is either polymerized in collagen matrix or provided soluble in the media (sHA). Here we report that collagen-embedded HA (eHA) inhibits EGFR activation, filopodia formation and cell spreading on a collagen matrix. These findings demonstrate a novel role for eHA as a protective molecule when encountered in the collagen matrix during cancer progression.

SUBMITTER: Louderbough JM 

PROVIDER: S-EPMC2852554 | biostudies-literature | 2010 Jan-Mar

REPOSITORIES: biostudies-literature

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Matrix hyaluronan alters epidermal growth factor receptor-dependent cell morphology.

Louderbough Jeanne M V JM   Lopez Jose I JI   Schroeder Joyce A JA  

Cell adhesion & migration 20100129 1


EGFR, a critical regulator of oncogenic signaling during cancer progression, is capable of integrating multireceptor signaling pathways that promote metastasis. EGFR is subject to regulatory cues from the extracellular matrix (ECM), of which hyaluronan (HA) is a major component. In mammary tumors, HA is deposited in the ECM where it functions in biomechanical support and modulates intracellular signaling. We utilized a 3D collagen system in which HA is either polymerized in collagen matrix or pr  ...[more]

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