Hyaluronic Acid Influences Amino Acid Metabolism via Differential L‐Type Amino Acid Transporter 1 Expression in the U87‐Malignant Glioma Cell Line

Author:

Bale Ashwin A.1ORCID,Thammineni Swaroop2,Bhargava Rohit12345ORCID,Harley Brendan135ORCID

Affiliation:

1. Department of Chemical and Biomolecular Engineering University of Illinois, Urbana‐Champaign Urbana IL 61802 USA

2. Department of Bioengineering University of Illinois, Urbana‐Champaign Urbana IL 61802 USA

3. Cancer Center at Illinois University of Illinois, Urbana‐Champaign Urbana IL 61802 USA

4. Departments of Electrical & Computer Engineering Mechanical Science & Engineering, and Chemistry Beckman Institute for Advanced Science and Technology University of Illinois, Urbana‐Champaign Urbana IL 61802 USA

5. Carl R. Woese Institute for Genomic Biology University of Illinois, Urbana‐Champaign Urbana IL 61802 USA

Abstract

The glioblastoma (GBM) tumor microenvironment is heterogeneous, complex, and being increasingly understood as a significant contributor to tumor progression. In brain tumors, the extracellular matrix contains a large concentration of hyaluronic acid (HA) that makes it important to study its role in cancer progression. In particular, abnormal accumulation of HA is observed in gliomas and is often associated with poor prognosis. In addition, HA is a polymer and its molecular weight (MW) distribution may influence tumor cell activity. Herein, the influence of the MW of HA on tumor cell metabolism is evaluated. A 2D cell culture approach is used to expose the U87‐MG (medium glucose [MG]) cell line to different HA MWs (10, 60, and 500 kDa) and glucose concentrations (0, 5.5, and 25 mm). Notably, it is found that HA influences GBM amino acid metabolism via reduction in LAT1 transporter protein expression. Also an influence on mitochondrial respiration levels and a difference in the accumulation of some key products of cell metabolic activity (lactic acid, glutamic acid, and succinic acid) are reported. Overall, in these results, it is indicated that HA MW can influence GBM metabolic state, with implications for cell invasion and tumor progression.

Funder

National Cancer Institute

University of Illinois at Urbana-Champaign

Publisher

Wiley

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