This Article Full Text Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Voelkel-Johnson, C. Articles by El-Zawahry, A. Search for Related Content PubMed PubMed Citation Articles by Voelkel-Johnson, C. Articles by El-Zawahry, A.

Departments of ¹ Microbiology and Immunology and ² Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, South Carolina

Requests for reprints: Christina Voelkel-Johnson, Department of Microbiology and Immunology, Medical University of South Carolina, P.O. Box 250504, 173 Ashley Avenue, Charleston, SC 29403. Phone: 843-792-3125; Fax: 843-792-2464. E-mail: johnsocv{at}musc.edu

Tumor necrosis factor–related apoptosis-inducing ligand (TRAIL) is a member of the tumor necrosis factor superfamily that selectively induces apoptosis in malignant cells. However, not all cancer cells are susceptible to TRAIL and mechanisms of resistance and new strategies to enhance sensitivity are an area of intense investigation. Glucose withdrawal or paclitaxel increase intracellular ceramide, down-regulate cellular FLICE inhibitory protein (cFLIP), and sensitize cells to TRAIL. Therefore, we investigated whether TRAIL resistance is due to ceramide levels and/or defects in ceramide generation following ligand binding. Colon cancer cells isolated from the primary tumor (SW480) and a subsequent metastasis (SW620) of the same patient have different sensitivities to TRAIL. Mass spectrometry was used to compare ceramide content in untreated and TRAIL-treated cells. Overall levels of ceramide were comparable in the cell lines but TRAIL-sensitive SW480 cells contained a higher percentage of C₁₆-, and C₁₈-ceramide and lower C₂₄-ceramides than TRAIL-resistant SW620 cells. Upon TRAIL treatment, ceramide (primarily C₁₆-ceramide) increased in SW480 but not SW620 cells. The increase in ceramide occurred with slow kinetics, paralleling caspase-3/7 activation. Combination of C₆-ceramide with TRAIL resulted in apoptosis of SW620 cells. However, exogenous C₆-ceramide did not affect levels of cFLIP nor did pretreatment sensitize cells to TRAIL. Exposure to TRAIL prior to ceramide was required to induce apoptosis, suggesting that ceramide plays a role in enhancing or amplifying TRAIL-mediated signaling. Our results suggest that ceramide plays a role in promoting TRAIL-mediated apoptosis and that TRAIL-resistant cancers may benefit from combination therapy with ceramide or agents that enhance ceramide accumulation.

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

³ H. Gosnell and C. Voelkel-Johnson, unpublished data

Received 3/24/05; revised 5/11/05; accepted 6/20/05.

This article has been cited by other articles:

				I. A. Savtchouk, F. J. Mattie, and A. A. Ollis Ceramide: From Embryos to Tumors Sci. Signal., September 2, 2008; 1(35): jc1 - jc1. [Abstract] [Full Text] [PDF]

				C. A. Corcoran, Q. He, S. Ponnusamy, B. Ogretmen, Y. Huang, and M. S. Sheikh Neutral Sphingomyelinase-3 Is a DNA Damage and Nongenotoxic Stress-Regulated Gene That Is Deregulated in Human Malignancies Mol. Cancer Res., May 1, 2008; 6(5): 795 - 807. [Abstract] [Full Text] [PDF]

				F. H. Psahoulia, K. G. Drosopoulos, L. Doubravska, L. Andera, and A. Pintzas Quercetin enhances TRAIL-mediated apoptosis in colon cancer cells by inducing the accumulation of death receptors in lipid rafts Mol. Cancer Ther., September 1, 2007; 6(9): 2591 - 2599. [Abstract] [Full Text] [PDF]

				I. A. Savtchouk, F. J. Mattie, and A. A. Ollis Ceramide: from Embryos to Tumors Sci. Signal., July 10, 2007; 2007(394): jc1 - jc1. [Abstract] [Full Text] [PDF]

				N. Finnberg and W. S. El-Deiry Selective TRAIL-Induced Apoptosis in Dysplastic Neoplasia of the Colon May Lead to New Neoadjuvant or Adjuvant Therapies. Clin. Cancer Res., July 15, 2006; 12(14): 4132 - 4136. [Full Text] [PDF]