Diabetic hyperglycemia promotes primary tumor progression through glycation-induced tumor extracellular matrix stiffening

Author:

Wang Wenjun1ORCID,Hapach Lauren A.12ORCID,Griggs Lauren3ORCID,Smart Kyra1ORCID,Wu Yusheng1,Taufalele Paul V.1,Rowe Matthew M.1ORCID,Young Katherine M.1,Bates Madison E.1ORCID,Johnson Andrew C.1ORCID,Ferrell Nicholas J.4ORCID,Pozzi Ambra56ORCID,Reinhart-King Cynthia A.12ORCID

Affiliation:

1. Department of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.

2. Nancy E. and Peter C. Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA.

3. College of Engineering, Pennsylvania State University, State College, PA 16802, USA.

4. Department of Internal Medicine, Division of Nephrology, Ohio State University Wexner Medical Center, Columbus, OH 43210, USA.

5. Division of Nephrology, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.

6. Veterans Affairs Hospitals, Nashville, TN 37684, USA.

Abstract

Diabetes mellitus is a complex metabolic disorder that is associated with an increased risk of breast cancer. Despite this correlation, the interplay between tumor progression and diabetes, particularly with regard to stiffening of the extracellular matrix, is still mechanistically unclear. Here, we established a murine model where hyperglycemia was induced before breast tumor development. Using the murine model, in vitro systems, and patient samples, we show that hyperglycemia increases tumor growth, extracellular matrix stiffness, glycation, and epithelial-mesenchymal transition of tumor cells. Upon inhibition of glycation or mechanotransduction in diabetic mice, these same metrics are reduced to levels comparable with nondiabetic tumors. Together, our study describes a novel biomechanical mechanism by which diabetic hyperglycemia promotes breast tumor progression via glycating the extracellular matrix. In addition, our work provides evidence that glycation inhibition is a potential adjuvant therapy for diabetic cancer patients due to the key role of matrix stiffening in both diseases.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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