Page 72 - SRPSKO DRUŠTVO ISTRAŽIVAČA RAKA
P. 72

Serbian Association for Cancer Research                                                       SDIRSACR

        6.  Wilschut, J.A.; Habbema, J.D.; van Leerdam, M.E.; Hol, L.; Lansdorp-Vogelaar, I.; Kuipers, E.J.; et al. Fecal occult
            blood testing when colonoscopy capacity is limited. J Natl Cancer Inst 2011, 103, 1741-51
        7.  Quintero, E.; Castells, A.; Bujanda, L.; Cubiella, J.; Salas, D.; Lanas, Á.; et al. Colonoscopy versus fecal immunochemical
            testing in colorectal-cancer screening. N Engl J Med 2012, 366, 697-706.
        8.  Young, G.P.; Rabeneck, L.; Winawer, S.J. The Global Paradigm Shift in Screening for Colorectal Cancer. Gastroenterology
            2019, 156, 843-851.
        9.  Robertson, D.J.; Lee, J.K.; Boland, C.R.; Dominitz, J.A.; Giardiello, F.M.; Johnson, D.A.; et al. Recommendations on
            Fecal Immunochemical Testing to Screen for Colorectal Neoplasia: A Consensus Statement by the US Multi-Society
            Task Force on Colorectal Cancer. Gastroenterology 2017, 152, 1217-1237.
        10. Murphy, N.; Moreno, V.; Hughes, D.J.; Vodicka, L.; Vodicka, P.; Aglago, E.K.; et al. Lifestyle and dietary environmental
            factors in colorectal cancer susceptibility. Mol Aspects Med 2019, 69, 2-9.
        11. Lichtenstein, P.; Holm, N.V.; Verkasalo, P.K.; Iliadou, A.; Kaprio, J.; Koskenvuo, M.; et al. Environmental and heritable
            factors in the causation of cancer–analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med
            2000, 343, 78-85
        12. Frank, C.; Sundquist, J.; Yu, H., Hemminki, A.; Hemminki, K. Concordant and discordant familial cancer: Familial
            risks, proportions and population impact. Int J Cancer 2017, 140, 1510-1516.
        13. Huyghe, J.R.; Bien, S.A.; Harrison, T.A.; Kang, H.M.; Chen, S.; Schmit, S.L.; et al. Discovery of common and rare
            genetic risk variants for colorectal cancer. Nat Genet 2019, 51, 76-87.
        14. Law, P.J.; Timofeeva, M.; Fernandez-Rozadilla, C.; Broderick, P.; Studd, J.; Fernandez-Tajes, J.; et al. Association
            analyses identify 31 new risk loci for colorectal cancer susceptibility. Nat Commun 2019, 10, 2154.
        15. Kraft, P.; Wacholder, S.; Cornelis, M.C.; Hu, F.B.; Hayes, R.B.; Thomas, G.; et al. Beyond odds ratios–communicating
            disease risk based on genetic profiles. Nat Rev Genet 2009, 10, 264-9.
        16. Dunlop, M.G.; Tenesa, A.; Farrington, S.M.; Ballereau, S.; Brewster, D.H.; Koessler, T.; et al. Cumulative impact of
            common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals. Gut 2013; 62, 871-81
        17. Jeon, J.; Du, M., Schoen, R.E.; Hoffmeister, M.; Newcomb, P.A.; Berndt, S.I.; et al. Determining Risk of Colorectal
            Cancer and Starting Age of Screening Based on Lifestyle, Environmental, and Genetic Factors. Gastroenterology
            2018, 154, 2152-2164.
        18. Thomas, M.; Sakoda, L.C.; Hoffmeister, M.; Rosenthal, E.A.; Lee, J.K.; van Duijnhoven, F.J.B.; et al. Genome-wide
            Modeling of Polygenic Risk Score in Colorectal Cancer Risk. Am J Hum Genet 2020, 107, 432-444
        19. Khera, A.V.; Chaffin, M.; Aragam, K.G.; Haas, M.E.; Roselli, C.; Choi, S.H.; et al. Genome-wide polygenic scores for
            common diseases identify individuals with risk equivalent to monogenic mutations. Nat Genet 2018, 50, 1219-
            1224.
        20. Frampton, M.J.; Law, P.; Litchfield, K.; Morris, E.J.; Kerr, D.; Turnbull, C.; et al. Implications of polygenic risk for
            personalised colorectal cancer screening. Ann Oncol 2016, 27, 429-34.
        21. Weigl, K.; Thomsen, H.; Balavarca, Y.; Hellwege, J.N.; Shrubsole, M.J.; Brenner, H. Genetic Risk Score Is Associated
            With Prevalence of Advanced Neoplasms in a Colorectal Cancer Screening Population. Gastroenterology 2018, 155,
            88-98.
        22. Guo, F.; Weigl, K.; Carr, P.R.; Heisser, T.; Jansen, L.; Knebel, P.; et al. Use of Polygenic Risk Scores to Select Screening
            Intervals After Negative Findings From Colonoscopy. Clin Gastroenterol Hepatol 2020, 18, 2742-2751.

        Acknowledgments and funding: This research was supported by grants from the Horizon Europe project STEPUPIORS
        (101079217;  HORIZON-WIDERA-2021-ACCESS-03),  Fondo  de  Investigación  Sanitaria/FEDER  (20/00113,  20/00226,
        23/00189), La Marató TV3 2019 (202008-10), Asociación Española Contra el Cáncer (PRYGN211085CAST), COST Action
        CA17118, “la Caixa” Foundation (agreement LCF/PR/SP23/52950009), CERCA Programme (Generalitat de Catalunya)
        and Agència de Gestió d'Ajuts Universitaris i de Recerca (Generalitat de Catalunya, 2021 SGR 01185). This work is
        supported (not financially) by the European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS).
        ERN GENTURIS is funded by the European Union. CIBEREHD is funded by the Instituto de Salud Carlos III.
        We are sincerely grateful to the patients, CNAG and Biobanks of all collaborating centers (Biobank of Hospital Clínic–
        IDIBAPS, Euskal Biobankoa), as well as to the Genomics facility of the Fundació de Recerca Clínic Barcelona-Institut
        d’Investigacions Biomèdiques August Pi i Sunyer (FRCB-IDIBAPS) for the technical help. This work was developed (in
        part) at the Esther Koplowitz Centre.












                                                                                                                   57
   67   68   69   70   71   72   73   74   75   76   77