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Deficient Pms2, ERCC1, Ku86, CcOI in Field Defects During Progression to Colon Cancer
Published on: July 28, 2010
Role of neutral ceramidase in colon cancer
Mónica García-Barros1,2, Nicolas Coant1,2, Toshihiko Kawamori3,4
1Department of Medicine, Stony Brook University, New York, USA.
Abstract:
Alterations in sphingolipid metabolism, especially ceramide and sphingosine 1-phosphate, have been linked to colon cancer, suggesting that enzymes of sphingolipid metabolism may emerge as novel regulators and targets in colon cancer. Neutral ceramidase (nCDase), a key enzyme in sphingolipid metabolism that hydrolyzes ceramide into sphingosine, is highly expressed in the intestine; however, its role in colon cancer has not been defined. Here we show that molecular and pharmacological inhibition of nCDase in colon cancer cells increases ceramide, and this is accompanied by decreased cell survival and increased apoptosis and autophagy, with minimal effects on noncancerous cells. Inhibition of nCDase resulted in loss of β-catenin and inhibition of ERK, components of pathways relevant for colon cancer development. Furthermore, inhibition of nCDase in a xenograft model delayed tumor growth and increased ceramide while decreasing proliferation. It is noteworthy that mice lacking nCDase treated with azoxymethane were protected from tumor formation. Taken together, these studies show that nCDase is pivotal for regulating initiation and development of colon cancer, and these data suggest that this enzyme is a suitable and novel target for colon cancer therapy.-García-Barros, M., Coant, N., Kawamori, T., Wada, M., Snider, A. J., Truman, J.-P., Wu, B. X., Furuya, H., Clarke, C. J., Bialkowska, A. B., Ghaleb, A., Yang, V. W., Obeid, L. M., Hannun, Y. A. Role of neutral ceramidase in colon cancer.
Insights
Neutral ceramidase (nCDase) inhibition in colon cancer cells increases ceramide, reducing cell survival and promoting apoptosis. Targeting nCDase shows promise for colon cancer therapy.
Area of Science:
- Biochemistry
- Oncology
- Molecular Biology
Background:
- Sphingolipid metabolism alterations, particularly ceramide and sphingosine 1-phosphate, are implicated in colon cancer.
- Neutral ceramidase (nCDase), which hydrolyzes ceramide to sphingosine, is highly expressed in the intestine but its role in colon cancer is undefined.
Purpose of the Study:
- To investigate the role of neutral ceramidase (nCDase) in colon cancer initiation and development.
- To evaluate nCDase as a potential therapeutic target for colon cancer.
Main Methods:
- Molecular and pharmacological inhibition of nCDase in colon cancer cell lines.
- Assessment of cell survival, apoptosis, autophagy, and key signaling pathways (β-catenin, ERK).
- Inhibition of nCDase in a colon cancer xenograft mouse model and evaluation of tumor growth, proliferation, and ceramide levels.
- Analysis of tumor formation in nCDase-deficient mice treated with azoxymethane.
Main Results:
- nCDase inhibition in colon cancer cells increased ceramide levels, decreased cell survival, and enhanced apoptosis and autophagy.
- Inhibition of nCDase led to loss of β-catenin and ERK signaling.
- nCDase inhibition in a xenograft model delayed tumor growth and reduced proliferation.
- nCDase-deficient mice were protected from azoxymethane-induced tumor formation.
Conclusions:
- Neutral ceramidase (nCDase) plays a pivotal role in regulating the initiation and progression of colon cancer.
- nCDase is a suitable and novel therapeutic target for colon cancer treatment.
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