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Fundamental Differences in Cell Cycle Deregulation in Human Papillomavirus-positive and Human Papillomavirus-negative Head/neck and Cervical Cancers

Overview
Journal Cancer Res
Specialty Oncology
Date 2007 May 19
PMID 17510386
Citations 259
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Abstract

Human papillomaviruses (HPV) are associated with nearly all cervical cancers, 20% to 30% of head and neck cancers (HNC), and other cancers. Because HNCs also arise in HPV-negative patients, this type of cancer provides unique opportunities to define similarities and differences of HPV-positive versus HPV-negative cancers arising in the same tissue. Here, we describe genome-wide expression profiling of 84 HNCs, cervical cancers, and site-matched normal epithelial samples in which we used laser capture microdissection to enrich samples for tumor-derived versus normal epithelial cells. This analysis revealed that HPV(+) HNCs and cervical cancers differed in their patterns of gene expression yet shared many changes compared with HPV(-) HNCs. Some of these shared changes were predicted, but many others were not. Notably, HPV(+) HNCs and cervical cancers were found to be up-regulated in their expression of a distinct and larger subset of cell cycle genes than that observed in HPV(-) HNC. Moreover, HPV(+) cancers overexpressed testis-specific genes that are normally expressed only in meiotic cells. Many, although not all, of the hallmark differences between HPV(+) HNC and HPV(-) HNC were a direct consequence of HPV and in particular the viral E6 and E7 oncogenes. This included a novel association of HPV oncogenes with testis-specific gene expression. These findings in primary human tumors provide novel biomarkers for early detection of HPV(+) and HPV(-) cancers, and emphasize the potential value of targeting E6 and E7 function, alone or combined with radiation and/or traditional chemotherapy, in the treatment of HPV(+) cancers.

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References
1.
Bartkova J, Lukas J, Muller H, Strauss M, Gusterson B, Bartek J . Abnormal patterns of D-type cyclin expression and G1 regulation in human head and neck cancer. Cancer Res. 1995; 55(4):949-56. View

2.
Furukawa Y, Terui Y, Sakoe K, Ohta M, Saito M . The role of cellular transcription factor E2F in the regulation of cdc2 mRNA expression and cell cycle control of human hematopoietic cells. J Biol Chem. 1994; 269(42):26249-58. View

3.
Geng Y, Eaton E, Picon M, Roberts J, Lundberg A, Gifford A . Regulation of cyclin E transcription by E2Fs and retinoblastoma protein. Oncogene. 1996; 12(6):1173-80. View

4.
Walboomers J, Meijer C . Do HPV-negative cervical carcinomas exist?. J Pathol. 1997; 181(3):253-4. DOI: 10.1002/(SICI)1096-9896(199703)181:3<253::AID-PATH755>3.0.CO;2-0. View

5.
Offenberg H, Schalk J, Meuwissen R, van Aalderen M, KESTER H, Dietrich A . SCP2: a major protein component of the axial elements of synaptonemal complexes of the rat. Nucleic Acids Res. 1998; 26(11):2572-9. PMC: 147596. DOI: 10.1093/nar/26.11.2572. View