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Sunderland Repository records the research produced by the University of Sunderland including practice-based research and theses.

AGE-modified basement membrane cooperates with Endo180 to promote epithelial cell invasiveness and decrease prostate cancer survival

Rodriguez-Teja, m, Gronau, JH, Breit, C, Zhang, YZ, Minamidate, A, Caley, MP, McCarthy, A, Cox, TR, Erler, JT, Gaughan, L, Darby, Steven, Robson, CN, Mauri, F, Waxman, J and Sturge, J (2015) AGE-modified basement membrane cooperates with Endo180 to promote epithelial cell invasiveness and decrease prostate cancer survival. Journal of Pathology, 235 (4). pp. 581-592. ISSN 1096-9896

Item Type: Article


Biomechanical strain imposed by age‐related thickening of the basal lamina and augmented tissue stiffness in the prostate gland coincides with increased cancer risk. Here we hypothesized that the structural alterations in the basal lamina associated with age can induce mechanotransduction pathways in prostate epithelial cells (PECs) to promote invasiveness and cancer progression. To demonstrate this, we developed a 3D model of PEC acini in which thickening and stiffening of basal lamina matrix was induced by advanced glycation end‐product (AGE)‐dependent non‐enzymatic crosslinking of its major components, collagen IV and laminin. We used this model to demonstrate that antibody targeted blockade of CTLD2, the second of eight C‐type lectin‐like domains in Endo180 (CD280, CLEC13E, KIAA0709, MRC2, TEM9, uPARAP) that can recognize glycosylated collagens, reversed actinomyosin‐based contractility [myosin‐light chain‐2 (MLC2) phosphorylation], loss of cell polarity, loss of cell–cell junctions, luminal infiltration and basal invasion induced by AGE‐modified basal lamina matrix in PEC acini. Our in vitro results were concordant with luminal occlusion of acini in the prostate glands of adult Endo180ΔEx2–6/ΔEx2–6 mice, with constitutively exposed CTLD2 and decreased survival of men with early (non‐invasive) prostate cancer with high epithelial Endo180 expression and levels of AGE. These findings indicate that AGE‐dependent modification of the basal lamina induces invasive behaviour in non‐transformed PECs via a molecular mechanism linked to cancer progression. This study provides a rationale for targeting CTLD2 in Endo180 in prostate cancer and other pathologies in which increased basal lamina thickness and tissue stiffness are driving factors.

Rodriguez-Teja_et_al-2015-The_Journal_of_Pathology.pdf - Published Version

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Depositing User: Steven Darby


Item ID: 6562
Identification Number:
ISSN: 1096-9896
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ORCID for Steven Darby: ORCID iD

Catalogue record

Date Deposited: 05 Aug 2016 08:31
Last Modified: 04 Feb 2021 19:16


Author: Steven Darby ORCID iD
Author: m Rodriguez-Teja
Author: JH Gronau
Author: C Breit
Author: YZ Zhang
Author: A Minamidate
Author: MP Caley
Author: A McCarthy
Author: TR Cox
Author: JT Erler
Author: L Gaughan
Author: CN Robson
Author: F Mauri
Author: J Waxman
Author: J Sturge

University Divisions

Faculty of Health Sciences and Wellbeing
Faculty of Health Sciences and Wellbeing > School of Pharmacy and Pharmaceutical Sciences


Sciences > Biomedical Sciences

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