Ecdysoneless Overexpression Drives Mammary Tumorigenesis through Upregulation of C-MYC and Glucose Metabolism

Abstract

Ecdysoneless (ECD) protein is essential for embryogenesis, cell-cycle progression, and cellular stress mitigation with an emerging role in mRNA biogenesis. We have previously shown that ECD protein as well as its mRNA are overexpressed in breast cancer and ECD overexpression predicts shorter survival in patients with breast cancer. However, the genetic evidence for an oncogenic role of ECD has not been established. Here, we generated transgenic mice with mammary epithelium-targeted overexpression of an inducible human ECD transgene (ECDTg). Significantly, ECDTg mice develop mammary hyperplasia, preneoplastic lesions, and heterogeneous tumors with occasional lung metastasis. ECDTg tumors exhibit epithelial to mesenchymal transition and cancer stem cell characteristics. Organoid cultures of ECDTg tumors showed ECD dependency for in vitro oncogenic phenotype and in vivo growth when implanted in mice. RNA sequencing (RNA-seq) analysis of ECDTg tumors showed a c-MYC signature, and alterations in ECD levels regulated c-MYC mRNA and protein levels as well as glucose metabolism. ECD knockdown-induced decrease in glucose uptake was rescued by overexpression of mouse ECD as well as c-MYC. Publicly available expression data analyses showed a significant correlation of ECD and c-MYC overexpression in breast cancer, and ECD and c-MYC coexpression exhibits worse survival in patients with breast cancer. Taken together, we establish a novel role of overexpressed ECD as an oncogenesis driver in the mouse mammary gland through upregulation of c-MYC–mediated glucose metabolism.

Document Details

Document Type
Pub Defense Publication
Publication Date
Jun 08, 2022
Source ID
10.1158/1541-7786.mcr-22-0122

Entities

People

  • Aditya Bele
  • Aniruddha Sarkar
  • Bhopal C. Mohapatra
  • Channabasavaiah Basavaraju Gurumurthy
  • Chittibabu Guda
  • Emad A. Rakha
  • Fang Qiu
  • Hamid Band
  • Irfana Saleem
  • K-U Wagner
  • Mansour Alsaleem
  • Matthew D Storck
  • Mohsin Raza
  • Pankaj K Singh
  • Robert Cardiff
  • Sai Sundeep Kollala
  • Sameer Mirza
  • Siddesh Southekal
  • Subodh M. Lele
  • Surendra K. Shukla
  • Vimla Band

Organizations

  • National Cancer Institute
  • National Institutes of Health
  • Qassim University
  • United States Department of Defense
  • University of California
  • University of Nebraska Medical Center
  • University of Nebraska–Lincoln
  • University of Nottingham

Tags

Fields of Study

  • Biology

Readers

  • Breast cancer cell signaling and growth regulation.
  • Critical Infrastructure Protection in CBRN and WMD Threats.
  • Molecular and genetic basis of cancer.

Technology Areas

  • Biotechnology