Genome of Helicobacter pylori and Serotype of HPV Detected in Oropharyngeal and Laryngeal Cancer and Chronic Inflammation Patients
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
34574466
PubMed Central
PMC8470705
DOI
10.3390/ijerph18189545
PII: ijerph18189545
Knihovny.cz E-zdroje
- Klíčová slova
- Helicobacter pylori, chronic inflammation, human papilloma virus, incidence, oropharynx, squamous cell carcinoma,
- MeSH
- Alphapapillomavirus * MeSH
- Helicobacter pylori * genetika MeSH
- infekce papilomavirem * epidemiologie MeSH
- infekce vyvolané Helicobacter pylori * epidemiologie MeSH
- lidé MeSH
- nádory hrtanu * MeSH
- orofarynx MeSH
- Papillomaviridae genetika MeSH
- séroskupina MeSH
- zánět MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
OBJECTIVE: Oropharyngeal/laryngeal carcinoma are common cancers of the upper aerodigestive system. Human papillomavirus (HPV) is described as the most frequent in the cancer of unknown primary. The presence of Helicobacter pylori (HP) in the oral cavity is discussed in some papers. THE AIM OF STUDY: To analyze the incidence of HPV and HP in oropharyngeal/laryngeal cancer persons versus persons with chronic tonsillar inflammation and healthy persons. METHODS: The samples were taken in three groups: (1) tissue of oropharynx/larynx cancer (103 specimens); (2) tissue of palatine tonsils (85 specimens); and (3) healthy control group (50 specimens). We analyzed the presence of HP (PCR) and HPV genomic DNA (Sacace HPV High-Risk Screen Real-TM Quant) in the samples. RESULTS: HP was detected in 86 samples (83.5%) and high-risk HPV in 62 samples (60.2%). We found a very high incidence of HP. In the cancer group, HP was detected in 82.5% cases and HPV positivity in 57.8%. In total, 7.2% of the cancer patients were negative for HP and HPV together. In turn, 53.6% of the cancer patients were positive for HP and HPV together. Four cases (4.2%) were positive for HPV only. VacA positivity was detected in 82 (79.6%) of the cancer cases and VacA negativity in 21 (20.4%) if the cancer cases. The incidence of HP in chronic inflammation (n = 85) was 65 cases (76.5%) and the incidence of HPV was 38 cases (44.7%). VacA positivity was detected in 59 (69.4%) of the chronic inflammation cases and VacA negativity was found in 26 (30.6%) of the chronic inflammation cases. Regarding the control group, we found HP positivity in 5 cases (11.1%) and HPV positivity in 19 cases (42.2%). There was VacA positivity in 6 cases (50.0%) of the control group. Statistically significantly lower prevalence of HP (p < 0.001) and HPV (p = 0.006) was found in the control group. CONCLUSIONS: We suggest that the palatine tonsils are colonized by HP. In our study, HP was present in oropharyngeal cancer in more cases in comparison with HPV infection. The presence of VacA from HP can have an influence on the human epithelial and immune cells' regulation ways. Our results do not support idea that the CagA-positive HP is a primary carcinogen in oropharyngeal area.
1st Faculty of Medicine Charles University 12108 Prague Czech Republic
3rd Faculty of Medicine Charles University 10000 Prague Czech Republic
Faculty of Biomedical Engineering Czech Technical University Prague 27201 Kladno Czech Republic
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Genç R., Çağlı S., Yüce I., Vural A., Okuducu H., Patıroğlu T., Güney E. The Role ofH. pyloriin the Development of Laryngeal Squamous Cell Carcinoma. Dis. Markers. 2013;35:447–449. doi: 10.1155/2013/950701. PubMed DOI PMC
Karczewska E., Konturek J.E., Konturek P.C., Cześnikiewicz M., Sito E., Bielański W., Kwiecień N., Obtułowicz W., Ziemniak W., Majka J., et al. Oral cavity as a potential source of gastric reinfection by Helicobacter pylori. Dig. Dis. Sci. 2002;47:978–986. doi: 10.1023/A:1015017502772. PubMed DOI
Burduk P.K. Association between infection of virulence cagA gene Helicobacter pylori and laryngeal squamous cell carcinoma. Med. Sci. Monit. 2013;19:584–591. doi: 10.12659/MSM.889011. PubMed DOI PMC
Sivars L., Tani E., Näsman A., Ramqvist T., Munck-Wikland E., Dalianis T. Human Papillomavirus as a Diagnostic and Prognostic Tool in Cancer of Unknown Primary in the Head and Neck Region. Anticancer. Res. 2016;36:487–493. PubMed
Ramqvist T., Mints M., Tertipis N., Näsman A., Romanitan M., Dalianis T. Studies on human papillomavirus (HPV) 16 E2, E5 and E7 mRNA in HPV-positive tonsillar and base of tongue cancer in relation to clinical outcome and immunological parameters. Oral. Oncol. 2015;51:1126–1131. doi: 10.1016/j.oraloncology.2015.09.007. PubMed DOI
Lim Y., Totsika M., Morrison M., Punyadeera C. Oral Microbiome: A New Biomarker Reservoir for Oral and Oropharyngeal Cancers. Theranostics. 2017;7:4313–4321. doi: 10.7150/thno.21804. PubMed DOI PMC
Bulut Y., Agacayak A., Karlidag T., Toraman Z.A., Yilmaz M. Association of cagA+ Helicobacter pylori with Adenotonsillar Hypertrophy. Tohoku J. Exp. Med. 2006;209:229–233. doi: 10.1620/tjem.209.229. PubMed DOI
Pavlík E., Lukeš P., Potužníková B., Astl J., Hrdá P., Souček A., Matucha P., Doseděl J., Šterzl I. Helicobacter pylori isolated from patients with tonsillar cancer or tonsillitis chronica could be of different genotype compared to isolates from gastrointestinal tract. Folia. Microbiol. 2007;52:91–94. doi: 10.1007/BF02932145. PubMed DOI
Abdel-Monem M.H., Magdy E., Nour Y.A., Harfoush R.A., Ibreak A. Detection of Helicobacter pylori in adenotonsillar tissue of children with chronic adenotonsillitis using rapid urease test, PCR and blood serology: A prospective study. Int. J. Pediatric Otorhinolaryngol. 2011;75:568–572. doi: 10.1016/j.ijporl.2011.01.021. PubMed DOI
Lukes P., Astl J., Pavlík E., Potuzníková B., Sterzl I., Betka J. Helicobacter pylori in tonsillar and adenoid tissue and its possible role in oropharyngeal carcinogenesis. Folia. Biol. 2008;54:33–39. PubMed
Chen M., Fang Y., Cheng L., Wu H. Helicobacter pylori is associated with poor prognosis of laryngeal precancerous lesion. Auris. Nasus. Larynx. 2020;47:268–275. doi: 10.1016/j.anl.2019.08.004. PubMed DOI
Pandey S., Follin-Arbelet B., Pun C.B., Gautam D.K., Johannessen A.C., Petersen F.C., Costea D.E., Sapkota D. Helicobacter pylori was not detected in oral squamous cell carcinomas from cohorts of Norwegian and Nepalese patients. Sci. Rep. 2020;10:8737. doi: 10.1038/s41598-020-65694-7. PubMed DOI PMC
Fellmann J., Weisert J.U., Soltermann A., Morand G., Morra L., Moch H., Huber G.F., Probst R. Helicobacter pylori detected in pharyngeal and laryngeal pathologies in patients with proven gastric colonization. Head Neck. 2013;36:1562–1566. doi: 10.1002/hed.23492. PubMed DOI
Nártová E., Kraus J., Pavlik E., Lukeš P., Katra R., Plzák J., Kolářová L., Šterzl I., Betka J., Astl J. Presence of different genotypes of Helicobacter pylori in patients with chronic tonsillitis and sleep apnoea syndrome. Eur. Arch. Oto-Rhino-Laryngol. 2014;271:607–613. doi: 10.1007/s00405-013-2607-9. PubMed DOI
Rotnáglová E., Tachezy R., Salakova M., Procházka B., Košl’abová E., Vesela E., Ludvíková V., Hamšíková E., Klozar J. HPV involvement in tonsillar cancer: Prognostic significance and clinically relevant markers. Int. J. Cancer. 2011;129:101–110. doi: 10.1002/ijc.25889. PubMed DOI
Berman T.A., Schiller J.T. Human papillomavirus in cervical cancer and oropharyngeal cancer: One cause, two diseases. Cancer. 2017;123:2219–2229. doi: 10.1002/cncr.30588. PubMed DOI
Simonidesova S., Hamsikova E., Ludvikova V., Klozar J., Vencalek O., Tachezy R. Prognostic value of posttreatment HPV-specific antibodies in patients with oropharyngeal tumors. J. Surg. Oncol. 2019;120:117–124. doi: 10.1002/jso.25473. PubMed DOI
Timbang M.R., Sim M.W., Bewley A.F., Farwell D.G., Mantravadi A., Moore M.G. HPV-related oropharyngeal cancer: A review on burden of the disease and opportunities for prevention and early detection. Hum. Vaccines Immunother. 2019;15:1920–1928. doi: 10.1080/21645515.2019.1600985. PubMed DOI PMC
D’Souza G., McNeel T., Fakhry C. Understanding personal risk of oropharyngeal cancer: Risk-groups for oncogenic oral HPV infection and oropharyngeal cancer. Ann. Oncol. 2017;28:3065–3069. doi: 10.1093/annonc/mdx535. PubMed DOI PMC
Wittekindt C., Klussmann J.P. Tumor Staging and HPV-Related Oropharyngeal Cancer. Adv. Struct. Saf. Stud. 2016;206:123–133. doi: 10.1007/978-3-319-43580-0_9. PubMed DOI
Lukeš P., Pavlik E., Potužníková B., Plzák J., Nártová E., Doseděl J., Katra R., Šterzl I., Betka J., Astl J. Comparison of Helicobacter Pylori Genotypes Obtained from the Oropharynx and Stomach of the Same Individuals–A Pilot Study. Prague Med. Rep. 2012;113:231–239. doi: 10.14712/23362936.2015.21. PubMed DOI
Lukeš P., Pavlik E., Potuznikova B., Nartova E., Foltynova E., Plzák J., Katra R., Sterzl I., Bartunkova J., Betka J., et al. Detection of Helicobacter pylori in oropharyngeal lymphatic tissue with real-time PCR and assessment of its carcinogenic potential. Eur. Arch. Oto-Rhino-Laryngol. 2014;271:399–405. doi: 10.1007/s00405-013-2574-1. PubMed DOI
Katra R., Kabelka Z., Jurovcik M., Hradsky O., Kraus J., Pavlik E., Nartova E., Lukeš P., Astl J. Pilot study: Association between Helicobacter pylori in adenoid hyperplasia and reflux episodes detected by multiple intraluminal impedance in children. Int. J. Pediatric Otorhinolaryngol. 2014;78:1243–1249. doi: 10.1016/j.ijporl.2014.04.040. PubMed DOI
Chen J., Domingue J.C., Sears C.L. Microbiota dysbiosis in select human cancers: Evidence of association and causality. Semin. Immunol. 2017;32:25–34. doi: 10.1016/j.smim.2017.08.001. PubMed DOI PMC
Lopez E.M., Tanner A.M., Du E., Patel S.N., Weiss J., Weissler M.C., Hackman T., Gupta G.P., Zevallos J., Elmore S., et al. Decline in circulating viral and human tumor markers after resection of head and neck carcinoma. Head Neck. 2021;43:27–34. doi: 10.1002/hed.26444. PubMed DOI
De Martel C., Ferlay J., Franceschi S., Vignat J., Bray F., Forman D., Plummer M. Global burden of cancers attributable to infections in 2008: A review and synthetic analysis. Lancet Oncol. 2012;13:607–615. doi: 10.1016/S1470-2045(12)70137-7. PubMed DOI
Ang K.K., Harris J., Wheeler R., Weber R., Rosenthal D.I., Nguyen-Tân P.F., Westra W.H., Chung C.H., Jordan R.C., Lu C., et al. Human Papillomavirus and Survival of Patients with Oropharyngeal Cancer. N. Engl. J. Med. 2010;363:24–35. doi: 10.1056/NEJMoa0912217. PubMed DOI PMC
Payão L.T.R.S.L.M. Helicobacter pyloriand its reservoirs: A correlation with the gastric infection. World J. Gastrointest. Pharmacol. Ther. 2016;7:126–132. doi: 10.4292/wjgpt.v7.i1.126. PubMed DOI PMC
Hwang M.S., Forman S.N., Kanter J.A., Friedman M. Tonsillar Helicobacter pylori Colonization in Chronic Tonsillitis. JAMA Otolaryngol. Neck Surg. 2015;141:245. doi: 10.1001/jamaoto.2014.3296. PubMed DOI
Siupsinskiene N., Katutiene I., Jonikiene V., Janciauskas D., Vaitkus S. Helicobacter pylori in the tonsillar tissue: A possible association with chronic tonsillitis and laryngopharyngeal reflux. J. Laryngol. Otol. 2017;131:549–556. doi: 10.1017/S0022215117000597. PubMed DOI
Najafipour R., Ahmadpour F., Farivar T.N., Pahlevan A., Johari P., Safdarian F., Mehr M.A. Assessment of Helicobacter pylori prevalence by scorpion real-time PCR in chronic tonsillitis patients. J. Glob. Infect. Dis. 2012;4:38–42. doi: 10.4103/0974-777X.93760. PubMed DOI PMC
Song Q., Lange T., Spahr A., Adler G., Bode G. Characteristic distribution pattern of Helicobacter pylori in dental plaque and saliva detected with nested PCR. J. Med. Microbiol. 2000;49:349–353. doi: 10.1099/0022-1317-49-4-349. PubMed DOI
Tang K.D., Vasani S., Menezes L., Taheri T., Walsh L.J., Hughes B.G., Frazer I.H., Kenny L., Scheper G.C., Punyadeera C. Oral HPV16 DNA as a screening tool to detect early oropharyngeal squamous cell carcinoma. Cancer Sci. 2020;111:3854–3861. doi: 10.1111/cas.14585. PubMed DOI PMC
Hatakeyama M. Structure and function of Helicobacter pylori CagA, the first-identified bacterial protein involved in human cancer. Proc. Jpn. Acad. Ser. B. 2017;93:196–219. doi: 10.2183/pjab.93.013. PubMed DOI PMC
Basso D., Navaglia F., Brigato L., Piva M.G., Toma A., Greco E., Di Mario F., Galeotti F., Roveroni G., Corsini A., et al. Analysis of Helicobacter pylori vacA andcagA genotypes and serum antibody profile in benign and malignant gastroduodenal diseases. Gut. 1998;43:182–186. doi: 10.1136/gut.43.2.182. PubMed DOI PMC
Miehlke S., Kirsch C., Agha-Amiri K., Günther T., Lehn N., Malfertheiner P., Stolte M., Ehninger G., Bayerdörffer E. The Helicobacter pylori vacA s1, m1 genotype and cagA is associated with gastric carcinoma in Germany. Int. J. Cancer. 2000;87:322–327. doi: 10.1002/1097-0215(20000801)87:3<322::AID-IJC3>3.0.CO;2-M. PubMed DOI
Fahimi F., Tohidkia M.R., Fouladi M., Aghabeygi R., Samadi N., Omidi Y. Pleiotropic cytotoxicity of VacA toxin in host cells and its impact on immunotherapy. BioImpacts. 2017;7:59–71. doi: 10.15171/bi.2017.08. PubMed DOI PMC
Chauhan N., Tay A.C.Y., Marshall B.J., Jain U. Helicobacter pyloriVacA, a distinct toxin exerts diverse functionalities in numerous cells: An overview. Helicobacter. 2019;24:e12544. doi: 10.1111/hel.12544. PubMed DOI
Caston R.R., Sierra J.C., Foegeding N.J., Truelock M.D., Campbell A.M., Frick-Cheng A.E., Bimczok D., Wilson K.T., McClain M.S., Cover T.L. Functional Properties of Helicobacter pylori VacA Toxin m1 and m2 Variants. Infect. Immun. 2020;88:e00032-20. doi: 10.1128/IAI.00032-20. PubMed DOI PMC