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      Schistosome and liver fluke derived catechol-estrogens and helminth associated cancers

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          Abstract

          Infection with helminth parasites remains a persistent public health problem in developing countries. Three of these pathogens, the liver flukes Clonorchis sinensis, Opisthorchis viverrini and the blood fluke Schistosoma haematobium, are of particular concern due to their classification as Group 1 carcinogens: infection with these worms is carcinogenic. Using liquid chromatography-mass spectrometry (LC-MS/MS) approaches, we identified steroid hormone like (e.g., oxysterol-like, catechol estrogen quinone-like, etc.) metabolites and related DNA-adducts, apparently of parasite origin, in developmental stages including eggs of S. haematobium, in urine of people with urogenital schistosomiasis, and in the adult stage of O. viverrini. Since these kinds of sterol derivatives are metabolized to active quinones that can modify DNA, which in other contexts can lead to breast and other cancers, helminth parasite associated sterols might induce tumor-like phenotypes in the target cells susceptible to helminth parasite associated cancers, i.e., urothelial cells of the bladder in the case of urogenital schistosomiasis and the bile duct epithelia or cholangiocytes, in the case of O. viverrini and C. sinensis. Indeed we postulate that helminth induced cancers originate from parasite estrogen-host epithelial/urothelial cell chromosomal DNA adducts, and here we review recent findings that support this conjecture.

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          Exome sequencing identifies distinct mutational patterns in liver fluke-related and non-infection-related bile duct cancers.

          The impact of different carcinogenic exposures on the specific patterns of somatic mutation in human tumors remains unclear. To address this issue, we profiled 209 cholangiocarcinomas (CCAs) from Asia and Europe, including 108 cases caused by infection with the liver fluke Opisthorchis viverrini and 101 cases caused by non-O. viverrini-related etiologies. Whole-exome sequencing (n = 15) and prevalence screening (n = 194) identified recurrent somatic mutations in BAP1 and ARID1A, neither of which, to our knowledge, has previously been reported to be mutated in CCA. Comparisons between intrahepatic O. viverrini-related and non-O. viverrini-related CCAs demonstrated statistically significant differences in mutation patterns: BAP1, IDH1 and IDH2 were more frequently mutated in non-O. viverrini CCAs, whereas TP53 mutations showed the reciprocal pattern. Functional studies demonstrated tumor suppressive functions for BAP1 and ARID1A, establishing the role of chromatin modulators in CCA pathogenesis. These findings indicate that different causative etiologies may induce distinct somatic alterations, even within the same tumor type.
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            Whole-genome sequence of Schistosoma haematobium.

            Schistosomiasis is a neglected tropical disease caused by blood flukes (genus Schistosoma; schistosomes) and affecting 200 million people worldwide. No vaccines are available, and treatment relies on one drug, praziquantel. Schistosoma haematobium has come into the spotlight as a major cause of urogenital disease, as an agent linked to bladder cancer and as a predisposing factor for HIV/AIDS. The parasite is transmitted to humans from freshwater snails. Worms dwell in blood vessels and release eggs that become embedded in the bladder wall to elicit chronic immune-mediated disease and induce squamous cell carcinoma. Here we sequenced the 385-Mb genome of S. haematobium using Illumina-based technology at 74-fold coverage and compared it to sequences from related parasites. We included genome annotation based on function, gene ontology, networking and pathway mapping. This genome now provides an unprecedented resource for many fundamental research areas and shows great promise for the design of new disease interventions.
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              Estrogen and the risk of breast cancer.

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                Author and article information

                Contributors
                Journal
                Front Genet
                Front Genet
                Front. Genet.
                Frontiers in Genetics
                Frontiers Media S.A.
                1664-8021
                04 November 2014
                23 December 2014
                2014
                : 5
                : 444
                Affiliations
                [1] 1Center for Parasite Biology and Immunology, National Health Institute Doutor Ricardo Jorge Porto, Portugal
                [2] 2Center for the Study of Animal Science, Instituto de Ciências e Tecnologias Agrárias e Agroalimentares, University of Porto Porto, Portugal
                [3] 3Department of Chemistry and Biochemistry, Centro de Investigação em Química, University of Porto Porto, Portugal
                [4] 4Department of Health Promotion and Chronic Diseases, National Health Institute Doutor Ricardo Jorge Porto, Portugal
                [5] 5Tropical Disease Research Laboratory, Liver Fluke and Cholangiocarcinoma Research Center, Department of Pathology, Faculty of Medicine, Khon Kaen University Khon Kaen, Thailand
                [6] 6Experimental Pathology and Therapeutics Group, Portuguese Institute for Oncology of Porto Porto, Portugal
                [7] 7Research Center for Neglected Diseases of Poverty, Department of Microbiology, Immunology and Tropical Medicine, School of Medicine & Health Sciences, George Washington University Washington, DC, USA
                Author notes

                Edited by: John R. Battista, Louisiana State University, USA

                Reviewed by: Christoph Grunau, University of Perpignan Via Domitia, France; Emmitt Randolph Jolly, Case Western Reserve University, USA; Mariya Pakharukova, Institute of Cytology and Genetics, Russia

                *Correspondence: Paul J. Brindley, Research Center for Neglected Diseases of Poverty, Department of Microbiology, Immunology and Tropical Medicine, School of Medicine & Health Sciences, George Washington University, Ross Hall, Room 521, 2300 I (Eye) Street, Northwest, Washington, DC 20037, USA e-mail: pbrindley@ 123456gwu.edu

                This article was submitted to Evolutionary and Genomic Microbiology, a section of the journal Frontiers in Genetics.

                Article
                10.3389/fgene.2014.00444
                4274992
                25566326
                b9e96468-631e-49bb-ae23-4c3096b21f7a
                Copyright © 2014 Correia da Costa, Vale, Gouveia, Botelho, Sripa, Santos, Santos, Rinaldi and Brindley.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 08 August 2014
                : 04 December 2014
                Page count
                Figures: 2, Tables: 0, Equations: 0, References: 68, Pages: 7, Words: 0
                Categories
                Genetics
                Mini Review Article

                Genetics
                urogenital schistosomiasis,opisthorchiasis,catechol-estrogens,oxysterols,dna-adducts,neglected tropical disease-associated-cancer,squamous cell carcinoma of the bladder,cholangiocarcinoma

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