The Impact of Alcohol Consumption and Oral Microbiota on Upper Aerodigestive Tract Carcinomas: A Pilot Study

Author:

Fiore Marco1ORCID,Minni Antonio23,Cavalcanti Luca2ORCID,Raponi Giammarco4ORCID,Puggioni Gianluca4,Mattia Alessandro5ORCID,Gariglio Sara6ORCID,Colizza Andrea2ORCID,Meliante Piero Giuseppe2ORCID,Zoccali Federica2ORCID,Tarani Luigi7ORCID,Barbato Christian1ORCID,Lucarelli Marco89ORCID,Ceci Flavio Maria8ORCID,Francati Silvia8,Ferraguti Giampiero8ORCID,Ceccanti Mauro10ORCID,Petrella Carla1ORCID

Affiliation:

1. Institute of Biochemistry and Cell Biology (IBBC-CNR), Sapienza University Hospital Policlinico Umberto I, 00161 Roma, Italy

2. Department of Sensory Organs, Sapienza University of Rome, 00161 Roma, Italy

3. Division of Otolaryngology-Head and Neck Surgery, San Camillo de Lellis Hospital, ASL Rieti-Sapienza University, Viale Kennedy, 02100 Rieti, Italy

4. Laboratory for Clinical Microbiology, Sapienza University Hospital Policlinico Umberto I, 00161 Roma, Italy

5. Dipartimento della Pubblica Sicurezza, Direzione Centrale di Sanità, Centro di Ricerche e Laboratorio di Tossicologia Forense, Ministero dell’Interno, 00185 Roma, Italy

6. DIFAR—Department of Pharmacy, Università di Genova, Viale Cembrano 4, 16148 Genova, Italy

7. Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, 00161 Roma, Italy

8. Department of Experimental Medicine, Sapienza University of Rome, 00161 Roma, Italy

9. Pasteur Institute Cenci Bolognetti Foundation, Sapienza University of Rome, 00161 Roma, Italy

10. ASL Roma1, SITAC, Società Italiana per il Trattamento dell’Alcolismo e le sue Complicanze, 00100 Roma, Italy

Abstract

Alcohol consumption is associated with oxidative stress and an increased risk of carcinoma of the upper aero-digestive tract (UADT). Recently, it has been found that some microorganisms in the human oral cavity may locally metabolize ethanol, forming acetaldehyde, a carcinogenic metabolite of alcohol. In a cohort of patients first visited for UADT cancers, we estimated their alcohol consumption by measuring Ethyl Glucuronide/EtG (a long-lasting metabolite of ethanol) in the hair and carbohydrate-deficient transferrin/CDT (short-term index of alcohol intake) in the serum. Moreover, we analyzed, by culture-based methods, the presence of Neisseria subflava, Streptococcus mitis, Candida albicans, and glabrata (microorganisms generating acetaldehyde) in the oral cavity. According to the EtG values, we correlated drinking alcohol with endogenous oxidative stress and the investigated microorganism’s presence. We found that 55% of heavy drinkers presented microorganisms generating acetaldehyde locally. Moreover, we found that the presence of oral acetaldehyde-producing bacteria correlates with increased oxidative stress compared to patients without such bacteria. As for the study of alcohol dehydrogenase gene polymorphisms (the enzyme that transforms alcohol to acetaldehyde), we found that only the “CGTCGTCCC” haplotype was more frequent in the general population than in carcinoma patients. This pilot study suggests the importance of estimating alcohol consumption (EtG), the presence of bacteria producing acetaldehyde, and oxidative stress as risk factors for the onset of oral carcinomas.

Publisher

MDPI AG

Subject

Cell Biology,Clinical Biochemistry,Molecular Biology,Biochemistry,Physiology

Reference72 articles.

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