期刊论文详细信息
Infectious Agents and Cancer
Evaluation of a combined triple method to detect causative HPV in oral and oropharyngeal squamous cell carcinomas: p16 Immunohistochemistry, Consensus PCR HPV-DNA, and In Situ Hybridization
Pantaleo Bufo7  Stefania Staibano5  Franco M Buonaguro4  Maria Lina Tornesello4  Gaetano De Rosa5  Silvana Papagerakis1  Corrado Rubini2  Giuseppina Campisi6  Simona Cagiano7  Maria Carmela Pedicillo7  Gabriella Aquino8  Gerardo Botti8  Renato Franco8  Lorenzo Lo Muzio3  Angela Santoro7  Vito Rodolico9  Giuseppe Pannone7 
[1]Department of Otolaryngology - Head and Neck Surgery - Laboratory of Oral, Head and Neck Cancer Invasion and Metastasis, Medical School, University of Michigan Ann Arbor, Ann Arbor, MI, USA
[2]Sezione di Anatomia Patologica, Università Politecnica delle Marche, Ancona, Italy
[3]Department of Surgical Sciences - Section of Oral Pathology, University of Foggia, Foggia, Italy
[4]Laboratory of Molecular Biology and Viral Oncogenesis & AIDS Reference Center, Istituto Nazionale Tumori Fondazione G. Pascale, Via Mariano Semmola 1, 80131 Naples, Italy
[5]Dipartimento di Scienze Biomorfologiche e Funzionali, Università degli Studi di Napoli 'Federico II', Via Sergio Pansini 5, 80131 Naples, Italy
[6]Dipartimento di Scienze Stomatologiche, Università di Palermo, Via del Vespro 129, 90127 Palermo, Italy
[7]Department of Surgical Sciences - Section of Anatomic Pathology and Cytopathology, University of Foggia, Viale Luigi Pinto 1, 71122 Foggia, Italy
[8]Istituto Nazionale per lo Studio e la Cura dei Tumori - Fondazione 'G. Pascale', Naples, Italy
[9]Dipartimento di Scienze per la promozione della Salute - Sez. Anatomia Patologica, Università degli Studi di Palermo, A.O.U. Policlinico "P. Giaccone" - Via del Vespro 129, 90127 Palermo, Italy
关键词: Methylation-Specific PCR;    Epigenetic;    p16-IHC;    IHC;    Immunohistochemistry;    DNA consensus PCR;    HPV;    Human papillomavirus;    OPSCC;    OSCC;    HN-SCC;    Head and neck squamous cell carcinoma;   
Others  :  803941
DOI  :  10.1186/1750-9378-7-4
 received in 2011-12-15, accepted in 2012-02-29,  发布年份 2012
PDF
【 摘 要 】

Background

Recent emerging evidences identify Human Papillomavirus (HPV) related Head and Neck squamous cell carcinomas (HN-SCCs) as a separate subgroup among Head and Neck Cancers with different epidemiology, histopathological characteristics, therapeutic response to chemo-radiation treatment and clinical outcome. However, there is not a worldwide consensus on the methods to be used in clinical practice. The endpoint of this study was to demonstrate the reliability of a triple method which combines evaluation of: 1. p16 protein expression by immunohistochemistry (p16-IHC); 2. HPV-DNA genotyping by consensus HPV-DNA PCR methods (Consensus PCR); and 3 viral integration into the host by in situ hybridization method (ISH). This triple method has been applied to HN-SCC originated from oral cavity (OSCC) and oropharynx (OPSCC), the two anatomical sites in which high risk (HR) HPVs have been clearly implicated as etiologic factors. Methylation-Specific PCR (MSP) was performed to study inactivation of p16-CDKN2a locus by epigenetic events. Reliability of multiple methods was measured by Kappa statistics.

Results

All the HN-SCCs confirmed HPV positive by PCR and/or ISH were also p16 positive by IHC, with the latter showing a very high level of sensitivity as single test (100% in both OSCC and OPSCC) but lower specificity level (74% in OSCC and 93% in OPSCC).

Concordance analysis between ISH and Consensus PCR showed a faint agreement in OPSCC (κ = 0.38) and a moderate agreement in OSCC (κ = 0.44). Furthermore, the addition of double positive score (ISHpositive and Consensus PCR positive) increased significantly the specificity of HR-HPV detection on formalin-fixed paraffin embedded (FFPE) samples (100% in OSCC and 78.5% in OPSCC), but reduced the sensitivity (33% in OSCC and 60% in OPSCC). The significant reduction of sensitivity by the double method was compensated by a very high sensitivity of p16-IHC detection in the triple approach.

Conclusions

Although HR-HPVs detection is of utmost importance in clinical settings for the Head and Neck Cancer patients, there is no consensus on which to consider the 'golden standard' among the numerous detection methods available either as single test or combinations. Until recently, quantitative E6 RNA PCR has been considered the 'golden standard' since it was demonstrated to have very high accuracy level and very high statistical significance associated with prognostic parameters. In contrast, quantitative E6 DNA PCR has proven to have very high level of accuracy but lesser prognostic association with clinical outcome than the HPV E6 oncoprotein RNA PCR. However, although it is theoretically possible to perform quantitative PCR detection methods also on FFPE samples, they reach the maximum of accuracy on fresh frozen tissue. Furthermore, worldwide diagnostic laboratories have not all the same ability to analyze simultaneously both FFPE and fresh tissues with these quantitative molecular detection methods. Therefore, in the current clinical practice a p16-IHC test is considered as sufficient for HPV diagnostic in accordance with the recently published Head and Neck Cancer international guidelines. Although p16-IHC may serve as a good prognostic indicator, our study clearly demonstrated that it is not satisfactory when used exclusively as the only HPV detecting method. Adding ISH, although known as less sensitive than PCR-based detection methods, has the advantage to preserve the morphological context of HPV-DNA signals in FFPE samples and, thus increase the overall specificity of p16/Consensus PCR combination tests.

【 授权许可】

   
2012 Pannone et al; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20140708051535732.pdf 2326KB PDF download
Figure 5. 55KB Image download
Figure 4. 345KB Image download
Figure 3. 41KB Image download
Figure 2. 146KB Image download
Figure 1. 145KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

Figure 4.

Figure 5.

【 参考文献 】
  • [1]Gillison ML, Koch WM, Capone RB: Evidence for a causal association between human papillomavirus and a subset of Head and Neck Cancers. J Natl Cancer Inst 2000, 92:709-720.
  • [2]Lo Muzio L, Campisi G, Giovannelli L, Ammatuna P, Greco I, Staibano S, Pannone G, De Rosa G, Di Liberto C, D' Angelo M: HPV-DNA and survivin expression in epithelial oral carcinogenesis: a relationship? Oral Oncol 2004, 40(7):736-741.
  • [3]Paz IB, Cook N, Odom-Maryon T, et al.: Human papillomavirus (HPV) in Head and Neck Cancer: an association of HPV 16 with squamous cell carcinoma of Waldeyer's tonsillar ring. Cancer 1997, 79:595-604.
  • [4]Ryerson AB, Peters ES, Coughlin SS, et al.: Burden of potentially human papillomavirus-associated cancers of the oropharynx and oral cavity in the US, 1998-2003. Cancer 2008, 113:2901-2909.
  • [5]Charfi L, Jouffroy T, de Cremoux P, et al.: Two types of squamous cell carcinoma of the palatine tonsil characterized by distinct etiology, molecular features and outcome. Cancer Lett 2008, 260:72-78.
  • [6]Pannone G, Santoro A, Papagerakis S, Lo Muzio L, De Rosa G, Bufo P: The role of human papillomavirus in the pathogenesis of head & neck squamous cell carcinoma: an overview. Infectious Agents and Cancer 2011, 6:4. BioMed Central Full Text
  • [7]Syrjänen K, Syrjänen S, Lamberg M, Pyrhönen S, Nuutinen J: Morphological and immunohistochemical evidence suggesting human papillomavirus (HPV) involvement in oral squamous cell carcinogenesis. Int J Oral Surg 1983, 12:418-424.
  • [8]Clifford GM, Smith JS, Plummer M, Munoz N, Franceschi S: Human papillomavirus types in invasive cervical cancer worldwide: a meta-analysis. Br J Cancer 2003, 88:63-73.
  • [9]Campisi G, Panzarella V, Giuliani M, Lajolo C, Di Fede O, Falaschini S, Di Liberto C, Scully C, Lo Muzio L: Human papillomavirus: its identity and controversial role in oral oncogenesis, premalignant and malignant lesions (review). Int J Oncol 2007, 30(4):813-823.
  • [10]Syrjänen S, Lodi G, von Bültzingslöwen I, Aliko A, Arduino P, Campisi G, Challacombe S, Ficarra G, Flaitz C, Zhou HM, Maeda H, Miller C, Jontell M: Human papillomaviruses in oral carcinoma and oral potentially malignant disorders: a systematic review. Oral Dis 2011, 17(S1):58-72.
  • [11]Termine N, Panzarella V, Falaschini S, Russo A, Matranga D, Lo Muzio L, Campisi G: HPV in oral squamous cell carcinoma vs Head and Neck squamous cell carcinoma biopsies: a meta-analysis (1988-2007). Ann Oncol 2008, 19(10):1681-1690.
  • [12]Cairns P, Polascik TJ, Eby Y, Tokino K, Califano J, Merlo A, Mao L, Herath J, Jenkins R, Westra W, et al.: Frequency of homozygous deletion at p16/CDKN2 in primary human tumours. Nat Genet 1995, 11(2):210-212.
  • [13]Merlo A, Herman JG, Mao L, Lee DJ, Gabrielson E, Burger PC, Baylin SB, Sidransky D: 5'CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers. Nat Med 1995, 1(7):686-692.
  • [14]Herman JG, Merlo A, Mao L, Lapidus RG, Issa JP, Davidson NE, Sidransky D, Baylin SB: Inactivation of the CDKN2/p16/MTS1 gene is frequently associated with aberrant DNA methylation in all common human cancers. Cancer Res 1995, 55(20):4525-4530.
  • [15]Gonzalez-Zulueta M, Bender CM, Yang AS, Nguyen T, Beart RW, Van Tornout JM, Jones PA: Methylation of the 5' CpG island of the p16/CDKN2 tumor suppressor gene in normal and transformed human tissues correlates with gene silencing. Cancer Res 1995, 55(20):4531-4535.
  • [16]Reed AL, Califano J, Cairns P, Westra WH, Jones RM, Koch W, Ahrendt S, Eby Y, Sewell D, Nawroz H, Bartek J, Sidransky D: High frequency of p16 (CDKN2/MTS-1/INK4A) inactivation in Head and Neck squamous cell carcinoma. Cancer Res 1996, 56(16):3630-3633.
  • [17]Rischin D, Young R, Fisher R, Le Q, Peters L, Choi J, O'Sullivan B, Giralt J, McArthur G: Prognostic significance of HPV and p16 status in patients with oropharyngeal cancer treated on a large international phase III trial [abstract]. J Clin Oncol 2009, 27(15s):Ab 6004.
  • [18]Reimers N, Kasper HU, Weissenborn SJ, et al.: Combined analysis of HPV-DNA, p16 and EGFR expression to predict prognosis in oropharyngeal cancer. Int J Cancer 2007, 120:1731-1738.
  • [19]National Comprehensive Cancer Network (NCCCN) Guidelines™ Version 1.2011-Head and Neck Cancers [http://www.nccn.org/professionals/physician_gls/f_guidelines.asp] webcite
  • [20]Umudum H, Rezanko T, Dag F, Dogruluk T: Human papillomavirus genome detection by in situ hybridization in fine-needle aspirates of metastatic lesions from head and neck squamous cell carcinomas. Cancer Cytopathol 2005, 105(3):171-177.
  • [21]El-Mofty SK, Zhang MQ, Davila RM: Histologic identification of human papillomavirus (HPV)-related squamous cell carcinoma in cervical lymph nodes: a reliable predictor of the site of an occult Head and Neck primary carcinoma. Head Neck Pathol 2008, 2(3):163-168.
  • [22]Pannone G, Santoro A, Carinci F, Bufo P, Papagerakis SM, Rubini C, Campisi G, Giovannelli L, Contaldo M, Serpico R, Mazzotta M, Lo Muzio L: Double demonstration of oncogenic high risk human papilloma virus DNA and HPV-E7 protein in oral cancers. Int J Immunopathol Pharmacol 2011, 24(S2):95-101.
  • [23]Scapoli L, Palmieri A, Rubini C, Martinelli M, Spinelli G, Ionna F, Carinci F: Low prevalence of human papillomavirus in squamous-cell carcinoma limited to oral cavity proper. Mod Pathol 2009, 22(3):366-372.
  • [24]Hines LE, Ceron-Cabrera D, Romero K, Anthony M, Woosley RL, Armstrong EP, Malone DC: Evaluation of warfarin drug interaction listings in US product information for warfarin and interacting drugs. Clin Ther 2011, 33(1):36-45.
  • [25]Amortegui AJ, Meyer MP, Elborne VL, Amin RM: p53, retinoblastoma gene product, and cyclin protein expression in human papillomavirus virus DNA-positive cervical intraepithelial neoplasia and invasive cancer. Mod Pathol 1995, 8(9):907-912.
  • [26]Keating JT, Cviko A, Riethdorf S, Riethdorf L, Quade BJ, Sun D, Duensing S, Sheets EE, Munger K, Crum CP: Ki-67, cyclin E, and p16INK4 are complimentary surrogate biomarkers for human papilloma virus-related cervical neoplasia. Am J Surg Pathol 2001, 25(7):884-891.
  • [27]O'Neill CJ, McCluggage WG: p16 expression in the female genital tract and its value in diagnosis. Adv Anat Pathol 2006, 13(1):8-15.
  • [28]Marur S, D'Souza G, Westra WH, Forastiere AA: HPV-associated Head and Neck Cancer: a virus-related cancer epidemic. Lancet Oncol 2010, 11(8):781-789.
  • [29]Fischer CA, Kampmann M, Zlobec I, Green E, Tornillo L, Lugli A, Wolfensberger M, Terracciano LM: p16 expression in oropharyngeal cancer: its impact on staging and prognosis compared with the conventional clinical staging parameters. Ann Oncol 2010, 21(10):1961-1966.
  • [30]Doxtader EE, Katzenstein AL: The relationship between p16 expression and high-risk human papillomavirus infection in squamous cell carcinomas from sites other than - uterine cervix: a study of 137 cases. Hum Pathol 2011, 43(3):327-332.
  • [31]El-Mofty SK, Lu DW: Prevalence of human papillomavirus type 16 DNA in squamous cell carcinoma of the palatine tonsil, and not the oral cavity, in young patients: a distinct clinicopathologic and molecular disease entity. Am J Surg Pathol 2003, 27:1463-1470.
  • [32]Cullen AP, Reid R, Campion M, Lörincz AT: Analysis of the physical state of different human papillomavirus DNAs in intraepithelial and invasive cervical neoplasm. J Virol 1991, 65:606-612.
  • [33]Dǚrst St M, Kleinheinz A, Hotz M, Gissmann L: The physical state of human papillomavirus type 16 DNA in benign and malignant genital tumours. J Gen Virol 1985, 66:1515-1522.
  • [34]Snijders PJ, Cromme FV, van den Brule AJ, Schrijnemakers HF, Snow GB, Meijer CJ, Walboomers JM: Prevalence and expression of human papillomavirus in tonsillar carcinomas, indicating a possible viral etiology. Int J Cancer 1992, 51(6):845-850.
  • [35]Mellin H, Dahlgren L, Munck-Wikland E, Lindholm J, Rabbani H, Kalantari M, et al.: Human papillomavirus type 16 is episomal and a high viral load may be correlated to better prognosis in tonsillar cancer. Int J Cancer 2002, 102:152-158.
  • [36]Prado JC, Calleja-Macias IE, Bernard HU, Kalantari M, Macay SA, Allan B, Williamson AL, Chung LP, Collins RJ, Zuna RE, Dunn ST, Ortiz-Lopez R, Barrera-Saldaña HA, Cubie HA, Cuschieri K, von Knebel-Doeberitz M, Sanchez GI, Bosch FX, Villa LL: Worldwide genomic diversity of the human papillomaviruses-53, 56, and 66, a group of high-risk HPVs unrelated to HPV16 and HPV-18. Virology 2005, 340(1):95-104.
  • [37]Kim SH, Koo BS, Kang S, Park K, Kim H, Lee KR, Lee MJ, Kim JM, Choi EC, Cho NH: HPV integration begins in the tonsillar crypt and leads to the alteration of p16, EGFR and c-myc during tumor formation. Int J Cancer 2007, 120(7):1418-1425.
  • [38]van Houten VM, Snijders PJ, van den Brekel MW: Biological evidence that human papillomaviruses are etiologically involved in a subgroup of Head and Neck squamous cell carcinomas. Int J Cancer 2001, 93:232-235.
  • [39]Klussmann JP, Weissenborn SJ, Wieland U, Dries V, Kolligs J, Jungehuelsing M, et al.: Prevalence, distribution, and viral load of human papillomavirus 16 DNA in tonsillar carcinomas. Cancer 2001, 92(11):2875-2884.
  • [40]Schache AG, Triantafilos Liloglou, Risk Janet M, Anastasia Filia, Jones Terence M, Jon Sheard, Woolgar Julia A, Helliwell Timothy R, Asterios Triantafyllou, Max Robinson, Philip Sloan, Colin Harvey-Woodworth, Daniel Sisson, Shaw Richard J: Evaluation of Human Papilloma Virus Diagnostic Testing in Oropharyngeal Squamous Cell Carcinoma: Sensitivity, Specificity, and Prognostic Discrimination. Clin Cancer Res 2011, 17:6262-6271.
  • [41]Greene FL, Page DL, Fleming ID, Fritz AG, Balch CM, Haller DG, et al.: American Joint Committee on Cancer. New York: Cancer Staging Manual. Springer; 2002.
  • [42]Husnjak K, Grce M, Magdić L, Pavelić K: Comparison of five different polymerase chain reaction methods for detection of human papillomavirus in cervical cell specimens. J Virol Methods 2000, 88(2):125-134.
  • [43]Cooper K, Herrington CS, Stickland JE, Evans MF, McGee JO: Episomal and integrated human papillomavirus in cervical neoplasia shown by non-isotopic in situ hybridization. J Clin Pathol 1991, 44:990-996.
  • [44]Evans MF, Mount SL, Beatty BG, Cooper K: Biotinyltyramide-based in situ hybridization signal patterns distinguish human papillomavirus type and grade of cervical intraepithelial neoplasia. Mod Pathol 2002, 15:1339-1347.
  • [45]Guo M, Gong Y, Deavers M, Silva EG, Jan YJ, Cogdell DE, Luthra R, Lin E, Lai HC, Zhang W, Sneige N: Evaluation of a commercialized in situ hybridization assay for detecting human papillomavirus DNA in tissue specimens from patients with cervical intraepithelial neoplasia and cervical carcinoma. J Clin Microbiol 2008, 46(1):274-280.
  • [46]Hopman AH, Kamps MA, Smedts F, Speel EJ, Herrington CS, Ramaekers FC: HPV in situ hybridization: impact of different protocols on the detection of integrated HPV. Int J Cancer 2005, 115(3):419-428.
  • [47]Hale CA, Fleiss JL: Interval estimation under two study designs for kappa with binary classifications. Biometrics 1993, 49(2):523-534.
  • [48]Nam JM: Interval estimation of the kappa coefficient with binary classification and an equal marginal probability model. Biometrics 2000, 56(2):583-585.
  • [49]Landis JR, Koch GG: The measurement of observer agreement for categorical data. Biometrics 1977, 33(1):159-174.
  文献评价指标  
  下载次数:14次 浏览次数:23次