Expression of colorectal neoplasia differentially expressed in anaplastic thyroid carcinoma and its effect on cancer

Lili Du1, Qingsong Zhao2, Jingjing Li1

  • 1Department of Endocrinology and Metabolism, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.

Abstract

Insights

Colorectal neoplasia differentially expressed (CRNDE) is highly expressed in anaplastic thyroid cancer (ATC), promoting cell proliferation. Targeting CRNDE may offer a new therapeutic strategy for ATC treatment.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Anaplastic thyroid cancer (ATC) has a high incidence among human cancers.
  • Colorectal neoplasia differentially expressed (CRNDE) is upregulated in various tumors, suggesting its potential as a therapeutic target.
  • The specific role of CRNDE in ATC remains largely unexplored.

Purpose of the Study:

  • To investigate the expression and function of CRNDE in anaplastic thyroid cancer.
  • To determine the impact of CRNDE on thyroid cancer patient prognosis.
  • To explore the potential of CRNDE as a molecular target for ATC therapy.

Main Methods:

  • Utilized Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) databases to analyze CRNDE expression in thyroid cancer (THCA).
  • Employed quantitative real-time PCR (qRT-PCR) to validate CRNDE expression in tumor and control tissues.
  • Conducted siRNA-mediated knockdown of CRNDE in ATC cell lines and analyzed cell proliferation, cell cycle, and key protein expressions.

Main Results:

  • CRNDE was found to be highly expressed in ATC tissues and associated with poor prognosis in THCA patients.
  • CRNDE knockdown in ATC cell lines (ARO) significantly reduced cell proliferation and induced G0/G1 cell cycle arrest.
  • CRNDE inhibition led to decreased expression of Wnt3a, β-catenin, and cyclin D1 proteins.

Conclusions:

  • High CRNDE expression in ATC may drive tumor cell proliferation via the Wnt/β-catenin signaling pathway.
  • CRNDE represents a promising molecular target for the development of novel anti-cancer therapies for ATC.

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