Background. In a previous analysis of head and neck squamous cell carcinomas (HNSCCs), we showed that the levels of the interferon-inducible protein IFI 16 inversely correlate with cancer grade. In this study, we further evaluate the molecular role of IF116 in the development of HNSCCs. Methods. The effect of IF116 expression was evaluated by its retroviral restoration in an IF116-negative HNSCC-derived cell line, HNO136, Growth rate and soft agar colony formation were evaluated. The effect of IF116 restoration in cells exposed to doxorubicin was also analyzed. Results. IF116 restoration resulted in the inhibition of both cell growth and in vitro transforming activity and increased doxorubicin-induced cell death by accumulating the cells at the G2/M phase. Conclusion. In agreement with our previous in vivo data, IF116appears to be involved in maintaining the normal growth of epithelial cells, whereas its downregulation may contribute uncontrolled cell proliferation and tumorigenesis.

Effects of IFI16 overexpression on the growth and doxorubicin sensitivity of head and neck squamous cell carcinoma-derived cell lines / M. DE ANDREA, D. Gioia, M. Mondini, B. Azzimonti, F. Reno', G. Pecorari, V. Landolfo, M. Tommasino, R. Accardi, C. HEROLD MENDE, S. Landolfo, M. Gariglio. - In: HEAD & NECK. - ISSN 1043-3074. - 29:9(2007), pp. 835-844. [10.1002/hed.20611]

Effects of IFI16 overexpression on the growth and doxorubicin sensitivity of head and neck squamous cell carcinoma-derived cell lines

F. Reno';
2007

Abstract

Background. In a previous analysis of head and neck squamous cell carcinomas (HNSCCs), we showed that the levels of the interferon-inducible protein IFI 16 inversely correlate with cancer grade. In this study, we further evaluate the molecular role of IF116 in the development of HNSCCs. Methods. The effect of IF116 expression was evaluated by its retroviral restoration in an IF116-negative HNSCC-derived cell line, HNO136, Growth rate and soft agar colony formation were evaluated. The effect of IF116 restoration in cells exposed to doxorubicin was also analyzed. Results. IF116 restoration resulted in the inhibition of both cell growth and in vitro transforming activity and increased doxorubicin-induced cell death by accumulating the cells at the G2/M phase. Conclusion. In agreement with our previous in vivo data, IF116appears to be involved in maintaining the normal growth of epithelial cells, whereas its downregulation may contribute uncontrolled cell proliferation and tumorigenesis.
Doxorubicin; Growth arrest; Head and neck squamous cell carcinoma; IFI16; Interferon
Settore BIO/16 - Anatomia Umana
2007
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1020281
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