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Updated: Aug 30, 2026

In vitro Organoid Culture of Primary Mouse Colon Tumors
Published on: May 17, 2013
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.
Abstract:
Phenethylisothiocyanate (PEITC), a potential cancer chemopreventive agent, induces colon cancer cell death, but the mechanism is not entirely clear. Therefore, the aim of this study was to further clarify the molecular effects of PEITC in causing death of human colon adenocarcinoma cells. When incubated with PEITC, HCT-116 colonocytes showed morphological features characteristic of apoptosis, such as irregular cell shape, translocation of plasma membrane phosphatidylserine, and also chromatin condensation and fragmentation. These changes occurred after single-strand breaks in DNA were detected, suggesting that PEITC induced irreparable DNA damage, which in turn triggered the process of apoptosis. DNA macroarray analysis of a selected small cluster of apoptosis-related genes revealed noticeably higher expression of only GADD45, which was confirmed by gene-specific relative RT-PCR analysis. This led to investigation of other GADD gene members possibly affected by PEITC. Whereas GADD34 mRNA expression increased just slightly, there was an appreciable elevation of the mRNA for GADD153, which is recognized as a pro-apoptotic gene. The effect of PEITC on GADD153 was attenuated by either actinomycin D or N-acetylcysteine, suggesting that PEITC-induced upregulation of GADD153 mRNA expression was partly at the level of transcriptional activation involving reactive oxygen species. Additionally, PEITC-induced upregulation of GADD153 mRNA expression did not appear to require p53, based on the observation that PEITC also increased GADD153 mRNA expression in HCT-15 colonocytes, which are known to express mutant p53. These findings suggest that PEITC creates an oxidative cellular environment that induces DNA damage and GADD153 gene activation, which in turn helps trigger apoptosis.
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.
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