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Published in: Infectious Agents and Cancer 1/2016

Open Access 01-12-2016 | Research Article

Salivary and serum IL-10, TNF-α, TGF-β, VEGF levels in oropharyngeal squamous cell carcinoma and correlation with HPV and EBV infections

Authors: Małgorzata Polz-Dacewicz, Małgorzata Strycharz-Dudziak, Jakub Dworzański, Agnieszka Stec, Joanna Kocot

Published in: Infectious Agents and Cancer | Issue 1/2016

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Abstract

Background

Each year approximately 6,000 new cases of head and neck cancer are registered in Poland. Human papillomavirus (HPV) and Epstein-Barr virus (EBV) have been associated with tumour formation. Cytokines have been shown to play an important role both in inflammation and carcinogenesis and they can be detected in saliva and serum with ELISA assays. Salivary biomarkers may be used as markers of early cancer detection.
The aim of this study was the analysis of the serum and salivary levels of IL-10, TNF-α, TGF-β and VEGF in patients with oropharyngeal cancer and in healthy individuals. The level of these biomarkers was also analyzed in HPV- and EBV-related cases.

Methods

The study involved 78 patients with histopathologically confirmed oropharyngeal squamous cell carcinoma and 40 healthy controls. Serum and salivary levels of IL-10, TNF-α, TGF-β and VEGF were analyzed both in patients and in healthy individuals by ELISA method using Diaclone SAS commercially available kits (France). EBV DNA was detected by the nested PCR for amplification of EBNA-2. HPV detection and genotyping was performed using the INNO-LiPA HPV Genotyping Extraassay (Innogenetics N. V, Gent, Belgium). The obtained results were subjected to statistical analysis using Mann–Whitney and Kruskal Wallis tests. Test values of p < 0.05 were considered statistically significant.

Results

The level of tested cytokines was higher in patients than in controls both in serum (IL-10: 2.3 pg/ml vs 1.65 pg/ml, p = 0.0003; TGF-β: 11.3 ng/ml vs 7.8 ng/ml, p = 0.0005; VEGF: 614 pg/ml vs 210 pg/ml, p = 0.0004; TNF-α: 15.0 ng/ml vs 12.90 ng/ml, p = 0.1397) as well as in saliva (IL-10: 5.9 pg/ml vs 2.5 pg/ml, p = 0.00002; TGF-β: 24.1 ng/ml vs 14.8 ng/ml, p = 0.00002; VEGF: 4321 pg/ml vs 280 pg/ml, p = 0.0000; TNF-α: 23.1 ng/ml vs 11.3 ng/ml, p = 0.00002).
EBV DNA was detected in 51.3 % of patients and 20 % of controls, HPV DNA was present in 30.8 % of patients and 2,5 % of controls.
The level of IL-10 was statistically higher in patients infected with EBV, HPV and co-infected with EBV/HPV. The level of TNF-α was significantly higher in patients infected with EBV, while TGF-β in patients with HPV infection and EBV/HPV co-infection.

Conclusion

Detection of salivary cytokines may be very helpful in early diagnosis, treatment and prognosis of OSCC.
Literature
1.
2.
3.
go back to reference Fakhry C, Westra WH, Li S, Cmelak A, Ridge JA, Pinto H, et al. Improved survival of patients with human papillomavirus-positive head and neck squamous cell carcinoma in a prospective clinical trials. J Natl Cancer Inst. 2008;100:261–9.CrossRefPubMed Fakhry C, Westra WH, Li S, Cmelak A, Ridge JA, Pinto H, et al. Improved survival of patients with human papillomavirus-positive head and neck squamous cell carcinoma in a prospective clinical trials. J Natl Cancer Inst. 2008;100:261–9.CrossRefPubMed
4.
go back to reference Gillison ML, Koch WM, Capone RB, Spafford M, Westra WH, Wu L, et al. Evidence for a causal association between human papillomavirus and a subset of head and neck cancers. J Natl Cancer Inst. 2000;92(9):709–20.CrossRefPubMed Gillison ML, Koch WM, Capone RB, Spafford M, Westra WH, Wu L, et al. Evidence for a causal association between human papillomavirus and a subset of head and neck cancers. J Natl Cancer Inst. 2000;92(9):709–20.CrossRefPubMed
5.
go back to reference Hillbertz NS, Hirsch JM, Jalouli J, Jalouli M, Sand L. Viral and molecular aspects of oral cancer. Anticancer Res. 2012;32(10):4201–12.PubMed Hillbertz NS, Hirsch JM, Jalouli J, Jalouli M, Sand L. Viral and molecular aspects of oral cancer. Anticancer Res. 2012;32(10):4201–12.PubMed
6.
go back to reference Scully C. Oral cancer aetiopathogenesis; past, present and future aspects. Med Oral Patol Oral Cir Bucal. 2011;16(3):e306–11.CrossRefPubMed Scully C. Oral cancer aetiopathogenesis; past, present and future aspects. Med Oral Patol Oral Cir Bucal. 2011;16(3):e306–11.CrossRefPubMed
7.
go back to reference Alibek K, Baiken Y, Kakpenova A, Mussabekova A, Zhussupbekova S, Akan M, et al. Implication of human herpesviruses in oncogenesis through immune evasion and supression. Infect Agent Cancer. 2014;9(1):3.CrossRefPubMedPubMedCentral Alibek K, Baiken Y, Kakpenova A, Mussabekova A, Zhussupbekova S, Akan M, et al. Implication of human herpesviruses in oncogenesis through immune evasion and supression. Infect Agent Cancer. 2014;9(1):3.CrossRefPubMedPubMedCentral
8.
go back to reference Schiller JT, Lowy DR. Virus infection and human cancer: an overview. Recent Results Cancer Res. 2014;193:1–10.CrossRefPubMed Schiller JT, Lowy DR. Virus infection and human cancer: an overview. Recent Results Cancer Res. 2014;193:1–10.CrossRefPubMed
9.
go back to reference IARC monographs on the evaluation of carcinogenic risks to humans. World Health Organization. Lyon, France, 2007; 222–235. IARC monographs on the evaluation of carcinogenic risks to humans. World Health Organization. Lyon, France, 2007; 222–235.
10.
go back to reference IARC monographs on the evaluation of carcinogenic risks to humans. A review of human carcinogens. Biological agents. World Health Organization. Lyon, France, 2012; 255–275. IARC monographs on the evaluation of carcinogenic risks to humans. A review of human carcinogens. Biological agents. World Health Organization. Lyon, France, 2012; 255–275.
11.
go back to reference Acharya S, Ekalaksananan T, Vatanasapt P, Loyha K, Phusingha P, Promthet S, et al. Association of Epstein-Barr virus infection with oral squamous cell carcinoma in a case–control study. J Oral Pathol Med. 2015;44:252–7.CrossRefPubMed Acharya S, Ekalaksananan T, Vatanasapt P, Loyha K, Phusingha P, Promthet S, et al. Association of Epstein-Barr virus infection with oral squamous cell carcinoma in a case–control study. J Oral Pathol Med. 2015;44:252–7.CrossRefPubMed
12.
go back to reference Jalouli J, Ibrahim SO, Mehrotra R, Jalouli MM, Sapkota D, Larson PA, Hirsch JM. Prevalence of viral (HPV, EBV, HSV) infections in oral submucous fibrosis and oral cancer from India. Acta Otolaryngol. 2010;130(11):1306–11.CrossRefPubMed Jalouli J, Ibrahim SO, Mehrotra R, Jalouli MM, Sapkota D, Larson PA, Hirsch JM. Prevalence of viral (HPV, EBV, HSV) infections in oral submucous fibrosis and oral cancer from India. Acta Otolaryngol. 2010;130(11):1306–11.CrossRefPubMed
13.
go back to reference Jalouli J, Jalouli MM, Sapkota D, Ibrahim SO, Larson PA, Sand L. Human papilloma virus, herpes simplex virus and Epstein-Barr virus in oral squamous cell carcinoma from eight different countries. Anticancer Res. 2012;32(2):571–80.PubMed Jalouli J, Jalouli MM, Sapkota D, Ibrahim SO, Larson PA, Sand L. Human papilloma virus, herpes simplex virus and Epstein-Barr virus in oral squamous cell carcinoma from eight different countries. Anticancer Res. 2012;32(2):571–80.PubMed
14.
go back to reference Kis A, Feher K, Gall T, Tar I, Boda R, Toth ED, et al. Epstein-Barr virus prevalence in oral squamous cell cancer and potentially malignant oral disorders in an eastern Hungarian population. Eur J Oral Sci. 2009;117(5):536–40.CrossRefPubMed Kis A, Feher K, Gall T, Tar I, Boda R, Toth ED, et al. Epstein-Barr virus prevalence in oral squamous cell cancer and potentially malignant oral disorders in an eastern Hungarian population. Eur J Oral Sci. 2009;117(5):536–40.CrossRefPubMed
15.
16.
go back to reference Jin L, Sturgis EM, Zhang Y, Huang Z, Song X, Chao X, et al. Association of tumor necrosis factor-alpha promoter variants with risk of HPV-associated oral squamous cell carcinoma. Mol Cancer. 2013;12:80.CrossRefPubMedPubMedCentral Jin L, Sturgis EM, Zhang Y, Huang Z, Song X, Chao X, et al. Association of tumor necrosis factor-alpha promoter variants with risk of HPV-associated oral squamous cell carcinoma. Mol Cancer. 2013;12:80.CrossRefPubMedPubMedCentral
17.
go back to reference Elashoff D, Zhou H, Reiss J, Wong J, Xiao H, Henson B, et al. Prevalidation of salivary biomarkers for oral cancer detection. Cancer Epidemiol Biomarkers Prev. 2012;21(4):664–72.CrossRefPubMedPubMedCentral Elashoff D, Zhou H, Reiss J, Wong J, Xiao H, Henson B, et al. Prevalidation of salivary biomarkers for oral cancer detection. Cancer Epidemiol Biomarkers Prev. 2012;21(4):664–72.CrossRefPubMedPubMedCentral
18.
go back to reference Korostoff A, Reder L, Masood R, Sinha UK. The role of salivary cytokine biomarkers in tongue cancer invasion and mortality. Oral Oncol. 2011;47(4):282–7.CrossRefPubMed Korostoff A, Reder L, Masood R, Sinha UK. The role of salivary cytokine biomarkers in tongue cancer invasion and mortality. Oral Oncol. 2011;47(4):282–7.CrossRefPubMed
19.
go back to reference Moser DM, Zhang X. Interleukin-10: new perspectives on an old cytokine. Immunol Rev. 2008;226:205–18.CrossRef Moser DM, Zhang X. Interleukin-10: new perspectives on an old cytokine. Immunol Rev. 2008;226:205–18.CrossRef
20.
go back to reference Torres-Poveda K, Bahena-Román M, Madrid-González C, Burquete-Garcia AI, Bermudez-Morales VH, Peralta-Zaragoza O, et al. Role of IL-10 and TGF-β1 in local immunosuppression in HPV-associated cervical neoplasia. World J Clin Oncol. 2014;5(4):753–63.CrossRefPubMedPubMedCentral Torres-Poveda K, Bahena-Román M, Madrid-González C, Burquete-Garcia AI, Bermudez-Morales VH, Peralta-Zaragoza O, et al. Role of IL-10 and TGF-β1 in local immunosuppression in HPV-associated cervical neoplasia. World J Clin Oncol. 2014;5(4):753–63.CrossRefPubMedPubMedCentral
21.
go back to reference Jin L, Sturgis EM, Cao X, Song X, Salahuddin T, Wei Q, et al. Interleukin-10 promoter variants predict HPV-positive tumors and survival of squamous cell carcinoma of the oropharynx. FASEB J. 2013;27(6):2496–503.CrossRefPubMedPubMedCentral Jin L, Sturgis EM, Cao X, Song X, Salahuddin T, Wei Q, et al. Interleukin-10 promoter variants predict HPV-positive tumors and survival of squamous cell carcinoma of the oropharynx. FASEB J. 2013;27(6):2496–503.CrossRefPubMedPubMedCentral
22.
go back to reference Goncalves AS, Arantes DA, Bernardes VF, Jaeger F, Silvia JM, Silvia TA, et al. Immunosuppresive mediators of oral squamous cell carcinoma in tumour samples and saliva. Hum Immunol. 2015;76(1):52–8.CrossRefPubMed Goncalves AS, Arantes DA, Bernardes VF, Jaeger F, Silvia JM, Silvia TA, et al. Immunosuppresive mediators of oral squamous cell carcinoma in tumour samples and saliva. Hum Immunol. 2015;76(1):52–8.CrossRefPubMed
23.
go back to reference Jiang C, Ye D, Qiu W, Zhang X, Zhang Z, He D, et al. Response of lymphocyte subsets and cytokines to Shenyang prescription in Sprague–Dawley rats with tongue squamous cell carcinomas induced by 4NQO. BMC Cancer. 2007;7:40.CrossRefPubMedPubMedCentral Jiang C, Ye D, Qiu W, Zhang X, Zhang Z, He D, et al. Response of lymphocyte subsets and cytokines to Shenyang prescription in Sprague–Dawley rats with tongue squamous cell carcinomas induced by 4NQO. BMC Cancer. 2007;7:40.CrossRefPubMedPubMedCentral
24.
go back to reference Lathers DM, Young MR. Increased aberrance of cytokine expression in plasma of patients with more advanced squamous cell carcinoma of the head and neck. Cytokine. 2004;25(5):220–8.CrossRefPubMed Lathers DM, Young MR. Increased aberrance of cytokine expression in plasma of patients with more advanced squamous cell carcinoma of the head and neck. Cytokine. 2004;25(5):220–8.CrossRefPubMed
25.
go back to reference Wajant H, Pfizenmaier K, Scheurich P. Tumor necrosis factor signaling. Cell Death Differ. 2003;10:45–65.CrossRefPubMed Wajant H, Pfizenmaier K, Scheurich P. Tumor necrosis factor signaling. Cell Death Differ. 2003;10:45–65.CrossRefPubMed
26.
27.
go back to reference Krishnan R, Thayalan DK, Padmanaban R, Ramadas R, Annasamy RK, Anandan N. Association of serum and salivary tumor necrosis factor-α with histological grading in oral cancer and its role in differentiating premalignant and malignant oral disease. Asian Pac J Cancer Prev. 2014;15(17):7141–8.CrossRefPubMed Krishnan R, Thayalan DK, Padmanaban R, Ramadas R, Annasamy RK, Anandan N. Association of serum and salivary tumor necrosis factor-α with histological grading in oral cancer and its role in differentiating premalignant and malignant oral disease. Asian Pac J Cancer Prev. 2014;15(17):7141–8.CrossRefPubMed
28.
go back to reference Juretić M, Cerović R, Belusoć-Gobić M, Brekalo Prso I, Kqiku L, Spalj S, et al. Salivary levels of TNF-α and IL-6 in patients with oral premalignant and malignant lesions. Folia Biol. 2013;59(2):99–102. Juretić M, Cerović R, Belusoć-Gobić M, Brekalo Prso I, Kqiku L, Spalj S, et al. Salivary levels of TNF-α and IL-6 in patients with oral premalignant and malignant lesions. Folia Biol. 2013;59(2):99–102.
29.
go back to reference Rhodus NL, Ho V, Miller CS, Myers S, Ondrey F. NF-kappaB dependent cytokine levels in saliva of patients with oral preneoplastic lesions and oral squamous cell carcinoma. Cancer Detect Prev. 2005;29(1):42–5.CrossRefPubMed Rhodus NL, Ho V, Miller CS, Myers S, Ondrey F. NF-kappaB dependent cytokine levels in saliva of patients with oral preneoplastic lesions and oral squamous cell carcinoma. Cancer Detect Prev. 2005;29(1):42–5.CrossRefPubMed
30.
go back to reference Piva MR, DE Souza LB, Martins-Filho PR, Nonaka CF, DE Santana ST, DE Souza Andrade ES, et al. Role of inflammation in oral carcinogenesis (Part II): CD8, FOXP3, TNF-α. TGF-β and NF-kB expression Oncol Lett. 2013;5(6):1909–14.PubMed Piva MR, DE Souza LB, Martins-Filho PR, Nonaka CF, DE Santana ST, DE Souza Andrade ES, et al. Role of inflammation in oral carcinogenesis (Part II): CD8, FOXP3, TNF-α. TGF-β and NF-kB expression Oncol Lett. 2013;5(6):1909–14.PubMed
32.
go back to reference Mincione G, Di Marcantonio MC, Artese L, Vianale G, Piccirelli A, Piccirelli M, et al. Loss of expression of TGF-beta1, TbetaRI and TbetaRII correlates with differentiation in human oral squamous cell carcinomas. Int J Oncol. 2008;32(2):323–31.PubMed Mincione G, Di Marcantonio MC, Artese L, Vianale G, Piccirelli A, Piccirelli M, et al. Loss of expression of TGF-beta1, TbetaRI and TbetaRII correlates with differentiation in human oral squamous cell carcinomas. Int J Oncol. 2008;32(2):323–31.PubMed
33.
go back to reference Friedrich RE, Klapdor R, Hagel C, Bartel-Friedrich S. Vascular endothelial growth factor (VEGF) in sera of oral and oropharyngeal squamous cell carcinoma patients. Anticancer Res. 2010;30(5):1765–6.PubMed Friedrich RE, Klapdor R, Hagel C, Bartel-Friedrich S. Vascular endothelial growth factor (VEGF) in sera of oral and oropharyngeal squamous cell carcinoma patients. Anticancer Res. 2010;30(5):1765–6.PubMed
34.
go back to reference Upile T, Jerjes W, Kafas P, Harini S, Singh SU, Guyer M, et al. Salivary VEGF: a non-invasive angiogenic and lymphangiogenic proxy in head and neck cancer prognostication. Int Arch Med. 2009;2(1):12.CrossRefPubMedPubMedCentral Upile T, Jerjes W, Kafas P, Harini S, Singh SU, Guyer M, et al. Salivary VEGF: a non-invasive angiogenic and lymphangiogenic proxy in head and neck cancer prognostication. Int Arch Med. 2009;2(1):12.CrossRefPubMedPubMedCentral
35.
go back to reference Ding L, Hu EL, Xu YJ, Huang XF, Zhang DY, Li B, et al. Serum IL-17F combined with VEGF as potential diagnostic biomarkers for oral squamous cell carcinoma. Tumour Biol. 2015;36(4):2523–9.CrossRefPubMed Ding L, Hu EL, Xu YJ, Huang XF, Zhang DY, Li B, et al. Serum IL-17F combined with VEGF as potential diagnostic biomarkers for oral squamous cell carcinoma. Tumour Biol. 2015;36(4):2523–9.CrossRefPubMed
36.
go back to reference Aggarwal S, Devaraja K, Sharma SC, Das SN. Expression of vascular endothelial growth factor (VEGF) in patients with oral squamous cell carcinoma and its clinical significance. Clin Chim Acta. 2014;436:35–40.CrossRefPubMed Aggarwal S, Devaraja K, Sharma SC, Das SN. Expression of vascular endothelial growth factor (VEGF) in patients with oral squamous cell carcinoma and its clinical significance. Clin Chim Acta. 2014;436:35–40.CrossRefPubMed
37.
go back to reference Andisheh-Tadbir A, Hamzavi M, Rezvani G, Ashraf MJ, Fattahi MJ, Khademi B, et al. Tissue expression, serum and salivary levels of vascular endothelial growth factor in patients with HNSCC. Braz J Otorhinolaryngol. 2014;80(6):503–7.CrossRefPubMed Andisheh-Tadbir A, Hamzavi M, Rezvani G, Ashraf MJ, Fattahi MJ, Khademi B, et al. Tissue expression, serum and salivary levels of vascular endothelial growth factor in patients with HNSCC. Braz J Otorhinolaryngol. 2014;80(6):503–7.CrossRefPubMed
38.
go back to reference Czerninski R, Basile JR, Kartin-Gabay T, Laviv A, Barak V. Cytokines and tumor markers in potentially malignant disorders and oral squamous cell carcinoma: a pilot study. Oral Dis. 2014;20(5):477–81.CrossRefPubMed Czerninski R, Basile JR, Kartin-Gabay T, Laviv A, Barak V. Cytokines and tumor markers in potentially malignant disorders and oral squamous cell carcinoma: a pilot study. Oral Dis. 2014;20(5):477–81.CrossRefPubMed
39.
go back to reference Tribius S, Hoffmann M. Human papilloma virus infection in head and neck cancer. Dtsch Arztebl Int. 2013;110(11):184–90.PubMedPubMedCentral Tribius S, Hoffmann M. Human papilloma virus infection in head and neck cancer. Dtsch Arztebl Int. 2013;110(11):184–90.PubMedPubMedCentral
40.
go back to reference Guan X, Sturgis EM, Lei D, Liu Z, Dahlstrom KR, Wei Q, et al. Association of TGF-beta1 genetic variants with HPV16-positive oropharyngeal cancer. Clin Cancer Res. 2010;16(5):1416–22.CrossRefPubMedPubMedCentral Guan X, Sturgis EM, Lei D, Liu Z, Dahlstrom KR, Wei Q, et al. Association of TGF-beta1 genetic variants with HPV16-positive oropharyngeal cancer. Clin Cancer Res. 2010;16(5):1416–22.CrossRefPubMedPubMedCentral
41.
go back to reference Chuang CY, Sung WW, Wang L, Lin WL, Yeh KT, Su MC, et al. Differential impact of IL-10 expression on survival and relapse between HPV16-positive and -negative oral squamous cell carcinomas. PLoS One. 2012;7(10):e47541.CrossRefPubMedPubMedCentral Chuang CY, Sung WW, Wang L, Lin WL, Yeh KT, Su MC, et al. Differential impact of IL-10 expression on survival and relapse between HPV16-positive and -negative oral squamous cell carcinomas. PLoS One. 2012;7(10):e47541.CrossRefPubMedPubMedCentral
42.
go back to reference Bermudez-Morales VH, Gutierrez LX, Alcocer-Gonzalez JM, Burguete A, Madrid-Marina V. Correlation between IL-10 gene expression and HPV infection in cervical cancer: a mechanism for immune response escape. Cancer Invest. 2008;26(10):1037–43.CrossRefPubMed Bermudez-Morales VH, Gutierrez LX, Alcocer-Gonzalez JM, Burguete A, Madrid-Marina V. Correlation between IL-10 gene expression and HPV infection in cervical cancer: a mechanism for immune response escape. Cancer Invest. 2008;26(10):1037–43.CrossRefPubMed
43.
go back to reference Jo S, Juhasz A, Zhang K, Ruel C, Loera S, Wilczynski SP, et al. Human papillomavirus infection as a prognostic factor in oropharyngeal squamous cell carcinomas treated in a prospective phase II clinical trial. Anticancer Res. 2009;29(5):1467–74.PubMedPubMedCentral Jo S, Juhasz A, Zhang K, Ruel C, Loera S, Wilczynski SP, et al. Human papillomavirus infection as a prognostic factor in oropharyngeal squamous cell carcinomas treated in a prospective phase II clinical trial. Anticancer Res. 2009;29(5):1467–74.PubMedPubMedCentral
44.
go back to reference Fei J, Hong A, Dobbins TA, Jones D, Lee CS, Loo C, et al. Prognostic significance of vascular endothelial growth factor in squamous cell carcinomas of the tonsil in relation to human papillomavirus status and epidermal growth factor receptor. Ann Surg Oncol. 2009;16(10):2908–17.CrossRefPubMed Fei J, Hong A, Dobbins TA, Jones D, Lee CS, Loo C, et al. Prognostic significance of vascular endothelial growth factor in squamous cell carcinomas of the tonsil in relation to human papillomavirus status and epidermal growth factor receptor. Ann Surg Oncol. 2009;16(10):2908–17.CrossRefPubMed
45.
go back to reference Chen CJ, Sung WW, Su TC, Chen MK, Wu PR, Yeh KT, et al. High expression of interleukin 10 might predict poor prognosis in early stage oral squamous cell carcinoma patients. Clin Chim Acta. 2013;415:25–30.CrossRefPubMed Chen CJ, Sung WW, Su TC, Chen MK, Wu PR, Yeh KT, et al. High expression of interleukin 10 might predict poor prognosis in early stage oral squamous cell carcinoma patients. Clin Chim Acta. 2013;415:25–30.CrossRefPubMed
46.
go back to reference Shi Y, Peng SL, Yang LF, Chen X, Tao YG, Cao Y. Co-infection of Epstein-Barr virus and human papillomavirus in tumorigenesis. Chin J Cancer. 2016;35(1):16.CrossRefPubMedPubMedCentral Shi Y, Peng SL, Yang LF, Chen X, Tao YG, Cao Y. Co-infection of Epstein-Barr virus and human papillomavirus in tumorigenesis. Chin J Cancer. 2016;35(1):16.CrossRefPubMedPubMedCentral
47.
go back to reference Odumade OA, Hogquist KA, Balfour Jr HH. Progress and problems in understanding and managing primary Epstein-Barr virus infections. Clin Microbiol Rev. 2011;24(1):193–209.CrossRefPubMedPubMedCentral Odumade OA, Hogquist KA, Balfour Jr HH. Progress and problems in understanding and managing primary Epstein-Barr virus infections. Clin Microbiol Rev. 2011;24(1):193–209.CrossRefPubMedPubMedCentral
48.
go back to reference Che AV, Lopez P, Pandofli PP, Roizman B. Promyelocytic leukemia protein mediates interferon-based anti-herpes simplex virus 1 effects. J Virol. 2003;77(12):7101–5.CrossRef Che AV, Lopez P, Pandofli PP, Roizman B. Promyelocytic leukemia protein mediates interferon-based anti-herpes simplex virus 1 effects. J Virol. 2003;77(12):7101–5.CrossRef
Metadata
Title
Salivary and serum IL-10, TNF-α, TGF-β, VEGF levels in oropharyngeal squamous cell carcinoma and correlation with HPV and EBV infections
Authors
Małgorzata Polz-Dacewicz
Małgorzata Strycharz-Dudziak
Jakub Dworzański
Agnieszka Stec
Joanna Kocot
Publication date
01-12-2016
Publisher
BioMed Central
Published in
Infectious Agents and Cancer / Issue 1/2016
Electronic ISSN: 1750-9378
DOI
https://doi.org/10.1186/s13027-016-0093-6

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