Induction of GADD gene expression by phenethylisothiocyanate in human colon adenocarcinoma cells

Anna Powolny1, Keiko Takahashi, Robin G Hopkins

  • 1Cellular and Molecular Nutrition Research Laboratory, Graduate Program in Nutrition, The University of North Carolina at Greensboro, Greensboro, North Carolina 27402-6170, USA.

Insights

Phenethylisothiocyanate (PEITC) triggers apoptosis in colon cancer cells by causing DNA damage and activating the GADD153 gene, potentially through an oxidative stress pathway. This research clarifies PEITC

Area of Science:

  • Molecular Biology
  • Cancer Research
  • Cell Biology

Background:

  • Phenethylisothiocyanate (PEITC) is a potential cancer chemopreventive agent.
  • The precise mechanism by which PEITC induces colon cancer cell death is not fully understood.

Purpose of the Study:

  • To elucidate the molecular mechanisms underlying PEITC-induced apoptosis in human colon adenocarcinoma cells.
  • To investigate the role of DNA damage and specific gene expression in PEITC's cytotoxic effects.

Main Methods:

  • Incubation of HCT-116 colonocytes with PEITC.
  • Assessment of morphological and biochemical markers of apoptosis.
  • DNA single-strand break detection.
  • DNA macroarray analysis and RT-PCR for apoptosis-related genes (GADD family).
  • Investigation of the role of reactive oxygen species and p53.

Main Results:

  • PEITC induced apoptosis in HCT-116 cells, evidenced by morphological changes and DNA fragmentation.
  • PEITC treatment led to single-strand DNA breaks, preceding apoptotic events.
  • Significant upregulation of GADD153 mRNA expression was observed, alongside minor increases in GADD34 and GADD45.
  • PEITC-induced GADD153 upregulation was partially dependent on reactive oxygen species and did not require functional p53.

Conclusions:

  • PEITC induces apoptosis in colon cancer cells through DNA damage and GADD153 gene activation.
  • An oxidative cellular environment and transcriptional activation involving reactive oxygen species contribute to GADD153 upregulation.
  • The p53 pathway is not essential for PEITC-mediated GADD153 induction in these colon cancer cells.

Related Concept Videos

Role Of Notch Signalling In Intestinal Stem Cell Renewal01:12

Role Of Notch Signalling In Intestinal Stem Cell Renewal

Notch signaling was first discovered in Drosophila melanogaster, where it is involved in cell lineage differentiation. Notch signaling regulates the maintenance and differentiation of intestinal stem cells or ISCs by controlling the expression of atonal homolog 1 or Atoh1. Atoh1 directs cells to differentiate into secretory cells.
Direct cell-to-cell contact is needed for the activation of Notch signaling. The signal is initiated when a notch ligand binds to a receptor on an adjacent cell, also...
Tumor Progression02:07

Tumor Progression

Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Cell Specific Gene Expression01:58

Cell Specific Gene Expression

Multicellular organisms contain a variety of structurally and functionally distinct cell types, but the DNA in all the cells originated from the same parent cells. The differences in the cells can be attributed to the differential gene expression. Liver cells, whose functions include detoxification of blood, production of bile to metabolize fats, and synthesis of proteins essential for metabolism, must express a specific set of genes to perform their functions. Gene expression also varies with...