Differential baseline and response profile to IFN-γ gene transduction of IL-6-IL-6 receptor-α secretion discriminate primary tumors versus bone marrow metastases of nasopharyngeal carcinomas in cultureReportar como inadecuado




Differential baseline and response profile to IFN-γ gene transduction of IL-6-IL-6 receptor-α secretion discriminate primary tumors versus bone marrow metastases of nasopharyngeal carcinomas in culture - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

BMC Cancer

, 9:169

First Online: 05 June 2009Received: 17 January 2009Accepted: 05 June 2009DOI: 10.1186-1471-2407-9-169

Cite this article as: Chou, A.SB., Wang, HY., Chen, HC. et al. BMC Cancer 2009 9: 169. doi:10.1186-1471-2407-9-169

Abstract

BackgroundUnderstanding of immunobiology of bone marrow metastases designated BM-NPC versus primary tumors P-NPC of the nasopharynx is far from complete. The aim of this study was to determine if there would be differences between cultured P-NPCs and BM-NPCs with respect to i constitutive IL-6 and the IL-6 receptor gp80 subunit IL-6Rα levels in the spent media of nontransduced cells, and ii IL-6 and IL-6Rα levels in the spent media of cells transduced with a retroviral vector containing the IFN-γ gene.

MethodsA panel of NPC cell lines were transduced with the IFN-γ gene through a retroviral vector. Four clonal sublines were isolated via limiting dilution methods. Cytofluorometric analysis was performed for the detection of cell surface antigens of HLA class I, HLA class II and ICAM-1. ELISA was used to assay for IFN-γ, IL-6 and IL-6Rα in the spent media of cultured cell lines.

ResultsOur results showed that in day 3 culture supernatants, low levels of soluble IL-6 were detected in 5-5 cultured tumors derived from P-NPCs, while much higher constitutive levels of IL-6 were detected in 3-3 metastasis-derived NPC cell lines including one originated from ascites; the difference was significant p = 0.025. An inverse relationship was found between IL-6Rα and IL-6 in their release levels in cultured P-NPCs and metastasis-derived NPCs. In IFN-γ-transduced-P-NPCs, IL-6 production increased and yet IL-6Rα decreased substantially, as compared to nontransduced counterparts. At variance with P-NPC cells, the respective ongoing IL-6 and IL-6Rα release patterns of BM-NPC cells were not impeded as much following IFN-γ transduction. These observations were confirmed by extended kinetic studies with representative NPC cell lines and clonal sublines. The latter observation with the clonal sublines also indicates that selection for high IL-6 or low IL-6Rα producing subpopulations did not occur as a result of IFN-γ-transduction process. P-NPCs, which secreted constitutively only marginal levels of IFN-γ 8.4 ~ 10.5 pg-ml, could be enhanced to produce higher levels of IFN-γ 6.8- to 10.3-fold increase after IFN-γ transduction. Unlike P-NPCs, BM-NPCs spontaneously released IFN-γ at moderate levels 83.8 ~ 100.7 pg-ml, which were enhanced by 1.3- to 2.2-fold in the spent media of their IFN-γ-transduced counterparts.

ConclusionOur results showed that cultured P-NPCs and BM-NPCs could be distinguished from one another on the basis of their differential baseline secretion pattern of IFN-γ, IL-6 and IL-6Rα, and their differential response profiles to IFN-γ gene transfer of the production of these three soluble molecules. These results suggest that the IL-6 and IFN-γ pathways in a background of genetic instability be involved in the acquisition of metastatic behaviour in BM-NPCs.

Electronic supplementary materialThe online version of this article doi:10.1186-1471-2407-9-169 contains supplementary material, which is available to authorized users.

Andy Shau-Bin Chou, Hsin-Yi Wang contributed equally to this work.

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Autor: Andy Shau-Bin Chou - Hsin-Yi Wang - Hung-Chang Chen - Ming-Hsiu Tsai - Cheng-Keng Chuang - Shuen-Kuei Liao

Fuente: https://link.springer.com/







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