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      Association of ABO and Rh blood groups with breast cancer

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          Abstract

          Objectives

          The aim of this study was to determine the association of “ABO” and “Rhesus” blood groups with incidence of breast cancer.

          Methods

          In this study, we identified 70 research documents from data based search engines including “PubMed”, “ISI-Web of Knowledge”, “Embase” and “Google Scholar”. The research papers were selected by using the primary key-terms including “ABO blood type”, “Rhesus” blood type and “breast cancer”. The research documents in which “ABO” and “Rhesus” blood types and breast cancer was debated were included. After screening, we reviewed 32 papers and finally we selected 25 research papers which met the inclusion criteria and remaining documents were excluded.

          Results

          Blood group “A” has high incidence of breast cancer (45.88%), blood group “O” has (31.69%); “B” (16.16%) and blood group “AB” has (6.27%) incidence of breast cancer. Blood group “A” has highest and blood group “AB” has least association with breast cancer. Furthermore, “Rhesus +ve” blood group has high incidence of breast cancer (88.31%) and “Rhesus –ve” blood group has least association with breast cancer (11.68%).

          Conclusion

          Blood group “A” and “Rhesus +ve” have high risk of breast cancer, while blood type “AB” and “Rhesus –ve” are at low peril of breast cancer. Physicians should carefully monitor the females with blood group “A” and “Rh +ve” as these females are more prone to develop breast cancer. To reduce breast cancer incidence and its burden, preventive and screening programs for breast cancer especially in young women are highly recommended.

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          Most cited references24

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          ABO blood group and the risk of pancreatic cancer.

          Other than several rare, highly penetrant familial syndromes, genetic risk factors for sporadic pancreatic cancer are largely unknown. ABO blood type is an inherited characteristic that in previous small studies has been associated with the risk of gastrointestinal malignancies. We separately examined the relationship between ABO blood type and the risk of incident pancreatic cancer in two large, independent, prospective cohort studies (the Nurses' Health Study and Health Professionals Follow-up Study) that collected blood group data on 107 503 US health professionals. Hazard ratios for pancreatic cancer by ABO blood type were calculated using Cox proportional hazards models with adjustment for other known risk factors, including age, tobacco use, body mass index, physical activity, and history of diabetes mellitus. All statistical tests were two-sided. During 927 995 person-years of follow-up, 316 participants developed pancreatic cancer. ABO blood type was associated with the risk of developing pancreatic cancer (P = .004; log-rank test). Compared with participants with blood group O, those with blood groups A, AB, or B were more likely to develop pancreatic cancer (adjusted hazard ratios for incident pancreatic cancer were 1.32 [95% confidence interval {CI} = 1.02 to 1.72], 1.51 [95% CI = 1.02 to 2.23], and 1.72 [95% CI = 1.25 to 2.38], respectively). The association between blood type and pancreatic cancer risk was nearly identical in the two cohorts (P(interaction) = .97). Overall, 17% of the pancreatic cancer cases were attributable to inheriting a non-O blood group (blood group A, B, or AB). The age-adjusted incidence rates for pancreatic cancer per 100 000 person-years were 27 (95% CI = 23 to 33) for participants with blood type O, 36 (95% CI = 26 to 50) for those with blood type A, 41 (95% CI = 31 to 56) for those with blood type AB, and 46 (95% CI = 32 to 68) for those with blood type B. In two large, independent populations, ABO blood type was statistically significantly associated with the risk of pancreatic cancer. Further studies are necessary to define the mechanisms by which ABO blood type or closely linked genetic variants may influence pancreatic cancer risk.
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            ABO blood groups and risk of cancer: a systematic review and meta-analysis.

            For decades, studies have been performed to evaluate the association between ABO blood groups and risk of cancer. However, whether ABO blood groups are associated with overall cancer risk remains unclear. We therefore conducted a meta-analysis of observational studies to assess this association.
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              A genome-wide association study identifies two susceptibility loci for duodenal ulcer in the Japanese population.

              Through a genome-wide association analysis with a total of 7,035 individuals with duodenal ulcer and 25,323 controls from Japan, we identified two susceptibility loci at the PSCA gene (encoding prostate stem cell antigen) at 8q24 and at the ABO blood group locus at 9q34. The C allele of rs2294008 at PSCA was associated with increased risk of duodenal ulcer (odds ratio (OR) = 1.84; P = 3.92 × 10(-33)) in a recessive model but was associated with decreased risk of gastric cancer (OR = 0.79; P = 6.79 × 10(-12)), as reported previously. The T allele of rs2294008 encodes a translation initiation codon upstream of the reported site and changes protein localization from the cytoplasm to the cell surface. rs505922 at ABO was also associated with duodenal ulcer in a recessive model (OR = 1.32; P = 1.15 × 10(-10)). Our findings demonstrate a role for genetic variants in the pathogenesis of duodenal ulcer.
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                Author and article information

                Contributors
                Journal
                Saudi J Biol Sci
                Saudi J Biol Sci
                Saudi Journal of Biological Sciences
                Elsevier
                1319-562X
                2213-7106
                03 February 2017
                November 2017
                03 February 2017
                : 24
                : 7
                : 1609-1613
                Affiliations
                [a ]Department of Physiology, College of Medicine, King Saud University, Riyadh, Saudi Arabia
                [b ]Department of Surgery (Plastic Surgery Division), College of Medicine, King Saud University, Riyadh, Saudi Arabia
                [c ]Department of Internal Medicine (Emergency Medicine), College of Medicine, King Saud University, Riyadh, Saudi Arabia
                [d ]Army Medical College, National University of Medical Sciences, Rawalpindi, Pakistan
                [e ]Department of Medical Education, College of Medicine, King Saud University, Riyadh, Saudi Arabia
                [f ]College of Food & Agriculture Sciences, King Saud University, Riyadh, Saudi Arabia
                [g ]Department of Obstetrics and Gynecology (IVF Division), College of Medicine, King Saud University, Riyadh, Saudi Arabia
                Author notes
                [* ]Corresponding author at: Department of Physiology, College of Medicine, King Saud University, Riyadh 11461, Saudi Arabia.Department of PhysiologyCollege of MedicineKing Saud UniversityRiyadh11461Saudi Arabia sultanmeo@ 123456hotmail.com smeo@ 123456ksu.edu.sa
                Article
                S1319-562X(17)30072-4
                10.1016/j.sjbs.2017.01.058
                5892599
                29657543
                b4a323d8-1d5a-4836-947b-7c7c94fe1dbc
                © 2017 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 15 December 2016
                : 9 January 2017
                : 25 January 2017
                Categories
                Article

                blood groups,abo blood groups,breast cancer
                blood groups, abo blood groups, breast cancer

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