Association between Blood Group and Nonmelanoma Skin Cancers (Basal Cell Carcinoma and Squamous Cell Carcinoma)

• Published in: International journal of environmental research and public health 2019-06, Vol.16 (13), p.2267
• Main Authors: Celić, Dijana, Lipozenčić, Jasna, Kolarić, Branko, Ferenčak, Goran, Rajković, Jolanda Kanižaj, Borlinić, Tajana
• Format: Article
• Language: English
• Subjects: ABO system; Adult; Age; Aged; Aged, 80 and over; Annual reports; Antigens; Biomarkers - blood; Bladder; Blood Group Antigens - adverse effects; Blood groups; Cancer therapies; Carcinoma, Basal Cell - blood; Carcinoma, Basal Cell - etiology; Carcinoma, Basal Cell - physiopathology; Carcinoma, Squamous Cell - blood; Carcinoma, Squamous Cell - etiology; Carcinoma, Squamous Cell - physiopathology; Cell adhesion & migration; Cell membranes; Cigarette smoking; Croatia; Demographics; Epithelial cells; Epithelium; Female; Genetics; Health care; Humans; Male; Melanoma; Metastases; Metastasis; Middle Aged; Phenotypes; Risk Factors; Skin cancer; Skin diseases; Skin Neoplasms - blood; Skin Neoplasms - etiology; Skin Neoplasms - physiopathology; Smoking; Squamous cell carcinoma; Sunburn & sun tanning; Tumors
• ISSN: 1660-4601; 1661-7827; 1660-4601
• DOI: 10.3390/ijerph16132267

Development of nonmelanoma skin cancers (NMSCs) has been associated with certain risk factors, but studies of the association between ABO blood group and NMSCs have been rare and inconclusive. The aim of this study was to assess the association of the previously known risk factors and blood group as a new potential risk factor in NMSCs. The study included 401 patients, 202 men, and 199 women, which included 367 diagnosed cases of basal cell carcinoma and 148 diagnosed cases of squamous cell carcinoma. The control group consisted of 438 subjects, 198 men, and 240 women. A standardized questionnaire adapted for this targeted study was used. The relation between the dependent variable (NMSCs) and independent variables was investigated by logistic regression. Compared to the non AB blood group, the risk of developing NMSCs was significantly higher in the AB blood group (MOR = 2.28; 95% CI = 1.41-3.69). We established a logistic model that could best describe the probability of NMSCs development. Study results are expected to instigate basic research into the role of A and B antigens in normal skin epithelium, NMSCs etiopathogenesis, possible effect on metastatic potential and disease prognosis, potential tumor immunotherapy, and targeted detection and prevention in subjects at an increased risk of NMSCs development.