Related Experiment Video
Updated: Aug 30, 2025

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
Published on: April 7, 2017
The Function of N-Myc Downstream-Regulated Gene 2 (NDRG2) as a Negative Regulator in Tumor Cell Metastasis
Ki Won Lee1, Seyeon Lim2, Kwang Dong Kim1,2,3
1Plant Molecular Biology and Biotechnology Research Center (PMBBRC), Gyeongsang National University, Jinju 52828, Korea.
Abstract:
N-myc downstream-regulated gene 2 (NDRG2) is a tumor-suppressor gene that suppresses tumorigenesis and metastasis of tumors and increases sensitivity to anti-cancer drugs. In this review, we summarize information on the clinicopathological characteristics of tumor patients according to NDRG2 expression in various tumor tissues and provide information on the metastasis inhibition-related cell signaling modulation by NDRG2. Loss of NDRG2 expression is a prognostic factor that correlates with TNM grade and tumor metastasis and has an inverse relationship with patient survival in various tumor patients. NDRG2 inhibits cell signaling, such as AKT-, NF-κB-, STAT3-, and TGF-β-mediated signaling, to induce tumor metastasis, and induces activation of GSK-3β which has anti-tumor effects. Although NDRG2 operates as an adaptor protein to mediate the interaction between kinases and phosphatases, which is essential in regulating cell signaling related to tumor metastasis, the molecular mechanism of NDRG2 as an adapter protein does not seem to be fully elucidated. This review aims to assist the research design regarding NDRG2 function as an adaptor protein and suggests NDRG2 as a molecular target to inhibit tumor metastasis and improve the prognosis in tumor patients.
Insights
N-myc downstream-regulated gene 2 (NDRG2) suppresses tumor growth and metastasis. Loss of NDRG2 expression worsens patient prognosis, highlighting its potential as a therapeutic target for inhibiting cancer spread.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- N-myc downstream-regulated gene 2 (NDRG2) functions as a tumor suppressor, inhibiting tumorigenesis and metastasis.
- NDRG2 expression levels correlate with patient prognosis and sensitivity to anti-cancer drugs.
- Loss of NDRG2 is linked to advanced tumor stage and metastasis across various cancers.
Purpose of the Study:
- To review clinicopathological characteristics associated with NDRG2 expression in tumors.
- To elucidate NDRG2's role in modulating cell signaling pathways involved in metastasis.
- To highlight NDRG2 as a potential molecular target for improving cancer prognosis.
Main Methods:
- Literature review and synthesis of existing research on NDRG2.
- Analysis of clinicopathological data correlating NDRG2 expression with tumor characteristics.
- Examination of molecular mechanisms by which NDRG2 regulates cell signaling pathways.
Main Results:
- Reduced NDRG2 expression is a prognostic indicator of poor survival and increased metastasis.
- NDRG2 inhibits key signaling pathways like AKT, NF-κB, STAT3, and TGF-β.
- NDRG2 activates GSK-3β, contributing to its anti-tumor effects.
- NDRG2 acts as an adaptor protein in regulating signaling pathways crucial for metastasis.
Conclusions:
- NDRG2 plays a critical role in suppressing tumor metastasis and improving patient outcomes.
- Understanding NDRG2's function as an adaptor protein is key to developing targeted therapies.
- NDRG2 represents a promising molecular target for inhibiting tumor metastasis and enhancing anti-cancer strategies.
More Related Videos
Related Concept Videos
Negative Regulator Molecules
Abnormal Proliferation
Mitogens and the Cell Cycle
Receptor Downregulation in MVBs
The EGFR can initiate signaling pathways that lead to cell proliferation, migration, and differentiation. Overexpression of EGFR stimulates cells to proliferate. Excessive EGFR...
Metastasis
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...

