A Novel Role of Connective Tissue Growth Factor in the Regulation of the Epithelial Phenotype

Author:

Gogoi Radhika P.1ORCID,Galoforo Sandra2,Fox Alexandra2,Morris Colton2,Ramos Harry2,Gogoi Vir K.2,Chehade Hussein2,Adzibolosu Nicholas K.2ORCID,Shi Chenjun3,Zhang Jitao3ORCID,Tedja Roslyn2ORCID,Morris Robert1,Alvero Ayesha B.2,Mor Gil2ORCID

Affiliation:

1. Karmanos Cancer Institute, Wayne State University, 4100 John R St, Detroit, MI 48202, USA

2. C.S. Mott Center for Human Growth and Development, Department of Obstetrics and Gynecology, Wayne State University, Detroit, MI 48202, USA

3. Department of Biomedical Engineering, Wayne State University, Detroit, MI 48202, USA

Abstract

Background: Epithelial–mesenchymal transition (EMT) is a biological process where epithelial cells lose their adhesive properties and gain invasive, metastatic, and mesenchymal properties. Maintaining the balance between the epithelial and mesenchymal stage is essential for tissue homeostasis. Many of the genes promoting mesenchymal transformation have been identified; however, our understanding of the genes responsible for maintaining the epithelial phenotype is limited. Our objective was to identify the genes responsible for maintaining the epithelial phenotype and inhibiting EMT. Methods: RNA seq was performed using an vitro model of EMT. CTGF expression was determined via qPCR and Western blot analysis. The knockout of CTGF was completed using the CTGF sgRNA CRISPR/CAS9. The tumorigenic potential was determined using NCG mice. Results: The knockout of CTGF in epithelial ovarian cancer cells leads to the acquisition of functional characteristics associated with the mesenchymal phenotype such as anoikis resistance, cytoskeleton remodeling, increased cell stiffness, and the acquisition of invasion and tumorigenic capacity. Conclusions: We identified CTGF is an important regulator of the epithelial phenotype, and its loss is associated with the early cellular modifications required for EMT. We describe a novel role for CTGF, regulating cytoskeleton and the extracellular matrix interactions necessary for the conservation of epithelial structure and function. These findings provide a new window into understanding the early stages of mesenchymal transformation.

Funder

Janet Burros Memorial Foundation

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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