4.7 Review

Epigenetic Regulation of the Biosynthesis & Enzymatic Modification of Heparan Sulfate Proteoglycans: Implications for Tumorigenesis and Cancer Biomarkers

Journal

Publisher

MDPI
DOI: 10.3390/ijms18071361

Keywords

biomarkers; biosynthetic pathways; enzymatic modification; epigenetic regulation; glycosylation; heparan sulfate proteoglycans; lectin arrays; sulfation

Funding

  1. research incentive grant

Ask authors/readers for more resources

Emerging evidence suggests that the enzymes in the biosynthetic pathway for the synthesis of heparan sulfate moieties of heparan sulfate proteoglycans (HSPGs) are epigenetically regulated at many levels. As the exact composition of the heparan sulfate portion of the resulting HSPG molecules is critical to the broad spectrum of biological processes involved in oncogenesis, the epigenetic regulation of heparan sulfate biosynthesis has far-reaching effects on many cellular activities related to cancer progression. Given the current focus on developing new anti-cancer therapeutics focused on epigenetic targets, it is important to understand the effects that these emerging therapeutics may have on the synthesis of HSPGs as alterations in HSPG composition may have profound and unanticipated effects. As an introduction, this review will briefly summarize the variety of important roles which HSPGs play in a wide-spectrum of cancer-related cellular and physiological functions and then describe the biosynthesis of the heparan sulfate chains of HSPGs, including how alterations observed in cancer cells serve as potential biomarkers. This review will then focus on detailing the multiple levels of epigenetic regulation of the enzymes in the heparan sulfate synthesis pathway with a particular focus on regulation by miRNA and effects of epigenetic therapies on HSPGs. We will also explore the use of lectins to detect differences in heparan sulfate composition and preview their potential diagnostic and prognostic use in the clinic.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Review Nutrition & Dietetics

Epigenetic Gene Regulation by Dietary Compounds in Cancer Prevention

McKale Montgomery, Aishwarya Srinivasan

ADVANCES IN NUTRITION (2019)

Article Nutrition & Dietetics

Distinct TP53 Mutation Subtypes Differentially Influence Cellular Iron Metabolism

Stephen L. Clarke, Laurie R. Thompson, Eshan Dandekar, Aishwarya Srinivasan, McKale R. Montgomery

NUTRIENTS (2019)

Article Biochemistry & Molecular Biology

Distinct TP53 Mutation Types Exhibit Increased Sensitivity to Ferroptosis Independently of Changes in Iron Regulatory Protein Activity

Laurie R. Thompson, Thais G. Oliveira, Evan R. Hermann, Winyoo Chowanadisai, Stephen L. Clarke, McKale R. Montgomery

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2020)

Article Cell Biology

Dual inhibition of TGFβR and ROCK reverses the epithelial to mesenchymal transition in collectively migrating zebrafish keratocytes

Agnes S. Pascual, Jose L. Rapanan, Chandana K. Uppalapati, Kimbal E. Cooper, Kathryn J. Leyva, Elizabeth E. Hull

Summary: Studies suggest that the appearance of fibroblasts and the production of extracellular matrix in fibrosis associated with chronic disease may be caused by differentiation of progenitor cells, response to chronic inflammation, or a combination of both, rather than the EMT transcriptional program. The EMT process in zebrafish keratocytes involves nuclear accumulation of twist and snail/slug transcription factors and is reversed by the addition of ROCK and TGF beta R inhibitors. The requirement for ROCK activation on noncompliant substrata suggests that EMT in terminally differentiated cells like keratocytes may not occur in vivo.

CELL BIOLOGY INTERNATIONAL (2021)

Article Genetics & Heredity

Brain Magnetic Resonance Imaging Phenome-Wide Association Study With Metal Transporter Gene SLC39A8

Evan R. Hermann, Emily Chambers, Danielle N. Davis, McKale R. Montgomery, Dingbo Lin, Winyoo Chowanadisai

Summary: The study identifies various brain MRI phenotypes associated with the SLC39A8 gene, with the missense ZIP8 polymorphism rs13107325 strongly linked to 22 brain MRI phenotypes. Rare ZIP8 variants are also associated with certain brain MRI phenotypes, in addition to new probable causative SNPs identified in the study. This provides insights into how genetic variation in SLC39A8 may influence brain structure and function.

FRONTIERS IN GENETICS (2021)

Article Biochemistry & Molecular Biology

HDAC inhibition induces EMT and alterations in cellular iron homeostasis to augment ferroptosis sensitivity in SW13 cells

Thais Oliveira, Evan Hermann, Daniel Lin, Winyoo Chowanadisai, Elizabeth Hull, McKale Montgomery

Summary: Epithelial-to-mesenchymal transition (EMT) is a crucial process in development and wound healing, but it can also contribute to the progression and spread of aggressive tumors in cancer, as well as increase resistance to therapy. This study used the SW13 cell line to investigate the connection between iron metabolism and EMT, finding that HDAC inhibitor treatment led to increased iron accumulation, reduced expression of iron export proteins, and enhanced sensitivity to a form of iron-mediated cell death called ferroptosis. These findings suggest potential implications for improving iron-targeted chemotherapeutic strategies in cancer treatment.

REDOX BIOLOGY (2021)

Article Biochemistry & Molecular Biology

A Hybrid Epithelial to Mesenchymal Transition in Ex Vivo Cutaneous Squamous Cell Carcinoma Tissues

Christopher S. Pulford, Chandana K. Uppalapati, McKale R. Montgomery, Richard L. Averitte, Elizabeth E. Hull, Kathryn J. Leyva

Summary: Studying patient-derived cSCC and adjacent normal tissues revealed a hybrid EMT process within individual cSCC tumors, where cells at the tumor edges displayed a more mesenchymal phenotype, while cells in the center maintained higher expression of epithelial markers. This dynamic may be regulated by miRNA and associated transcription factors, impacting therapeutic strategies for more invasive disease.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2022)

Article Cell Biology

Differences in Antioxidant and Lipid Handling Protein Expression Influence How Cells Expressing Distinct Mutant TP53 Subtypes Maintain Iron Homeostasis

Cameron J. Cardona, Evan R. Hermann, Kate N. Kouplen, Steven D. Hartson, McKale R. Montgomery

Summary: This study reveals the differences in cellular response to iron restriction among different TP53 mutation subtypes, and suggests that mutant TP53-dependent sensitivities to iron restriction are driven by differences in cellular antioxidant and lipid handling protein expression.

CELLS (2022)

Letter Endocrinology & Metabolism

Prevalence of metabolically healthy obesity in the United States: A cross-sectional evaluation of the National Health and Nutrition Examination Survey

Ashlea C. Braun, Micah L. Hartwell, McKale R. Montgomery, Sam R. Emerson, Katherine T. Morris, Benjamin H. Greiner

OBESITY RESEARCH & CLINICAL PRACTICE (2022)

Review Biochemistry & Molecular Biology

Iron regulatory proteins: players or pawns in ferroptosis and cancer?

Cameron J. Cardona, McKale R. Montgomery

Summary: Cells regulate the amount of iron within the body and in individual cells tightly, as iron can both promote cell proliferation and contribute to tumor initiation and growth. Iron regulatory proteins (IRPs) maintain iron homeostasis at the cellular level post-transcriptionally. Ferroptosis, an iron-dependent form of programmed cell death, has potential in chemotherapy, and there is a growing body of evidence suggesting that IRPs play critical roles in the adaptive response to ferroptosis and ferroptotic cell death.

FRONTIERS IN MOLECULAR BIOSCIENCES (2023)

Meeting Abstract Oncology

The contributions of iron regulatory proteins 1 and 2 to ferroptosis activation and ferroptotic cell death.

Evan Hermann, Thais Oliveira, McKale Montgomery

CANCER RESEARCH (2021)

Meeting Abstract Oncology

Induction of distinct p53 mutation types differentially influences the control of cellular iron metabolism

Eshan Dandekar, Aishwarya Srinivasan, Stephen Clarke, Mckale Montgomery

CANCER RESEARCH (2019)

No Data Available