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      A novel view on an old drug, 5-fluorouracil: an unexpected RNA modifier with intriguing impact on cancer cell fate

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          Abstract

          5-Fluorouracil (5-FU) is a chemotherapeutic drug widely used to treat patients with solid tumours, such as colorectal and pancreatic cancers. Colorectal cancer (CRC) is the second leading cause of cancer-related death and half of patients experience tumour recurrence. Used for over 60 years, 5-FU was long thought to exert its cytotoxic effects by altering DNA metabolism. However, 5-FU mode of action is more complex than previously anticipated since 5-FU is an extrinsic source of RNA modifications through its ability to be incorporated into most classes of RNA. In particular, a recent report highlighted that, by its integration into the most abundant RNA, namely ribosomal RNA (rRNA), 5-FU creates fluorinated active ribosomes and induces translational reprogramming. Here, we review the historical knowledge of 5-FU mode of action and discuss progress in the field of 5-FU-induced RNA modifications. The case of rRNA, the essential component of ribosome and translational activity, and the plasticity of which was recently associated with cancer, is highlighted. We propose that translational reprogramming, induced by 5-FU integration in ribosomes, contributes to 5-FU-driven cell plasticity and ultimately to relapse.

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          Graphical Abstract

          5-FU integration in ribosomes contributes to cell plasticity through translational reprogramming.

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          Global Cancer Statistics 2018: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries

          This article provides a status report on the global burden of cancer worldwide using the GLOBOCAN 2018 estimates of cancer incidence and mortality produced by the International Agency for Research on Cancer, with a focus on geographic variability across 20 world regions. There will be an estimated 18.1 million new cancer cases (17.0 million excluding nonmelanoma skin cancer) and 9.6 million cancer deaths (9.5 million excluding nonmelanoma skin cancer) in 2018. In both sexes combined, lung cancer is the most commonly diagnosed cancer (11.6% of the total cases) and the leading cause of cancer death (18.4% of the total cancer deaths), closely followed by female breast cancer (11.6%), prostate cancer (7.1%), and colorectal cancer (6.1%) for incidence and colorectal cancer (9.2%), stomach cancer (8.2%), and liver cancer (8.2%) for mortality. Lung cancer is the most frequent cancer and the leading cause of cancer death among males, followed by prostate and colorectal cancer (for incidence) and liver and stomach cancer (for mortality). Among females, breast cancer is the most commonly diagnosed cancer and the leading cause of cancer death, followed by colorectal and lung cancer (for incidence), and vice versa (for mortality); cervical cancer ranks fourth for both incidence and mortality. The most frequently diagnosed cancer and the leading cause of cancer death, however, substantially vary across countries and within each country depending on the degree of economic development and associated social and life style factors. It is noteworthy that high-quality cancer registry data, the basis for planning and implementing evidence-based cancer control programs, are not available in most low- and middle-income countries. The Global Initiative for Cancer Registry Development is an international partnership that supports better estimation, as well as the collection and use of local data, to prioritize and evaluate national cancer control efforts. CA: A Cancer Journal for Clinicians 2018;0:1-31. © 2018 American Cancer Society.
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            Projecting cancer incidence and deaths to 2030: the unexpected burden of thyroid, liver, and pancreas cancers in the United States.

            Cancer incidence and deaths in the United States were projected for the most common cancer types for the years 2020 and 2030 based on changing demographics and the average annual percentage changes in incidence and death rates. Breast, prostate, and lung cancers will remain the top cancer diagnoses throughout this time, but thyroid cancer will replace colorectal cancer as the fourth leading cancer diagnosis by 2030, and melanoma and uterine cancer will become the fifth and sixth most common cancers, respectively. Lung cancer is projected to remain the top cancer killer throughout this time period. However, pancreas and liver cancers are projected to surpass breast, prostate, and colorectal cancers to become the second and third leading causes of cancer-related death by 2030, respectively. Advances in screening, prevention, and treatment can change cancer incidence and/or death rates, but it will require a concerted effort by the research and healthcare communities now to effect a substantial change for the future. ©2014 American Association for Cancer Research.
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              Epidemiology of Pancreatic Cancer: Global Trends, Etiology and Risk Factors

              Pancreatic cancer is the seventh leading cause of cancer-related deaths worldwide. However, its toll is higher in more developed countries. Reasons for vast differences in mortality rates of pancreatic cancer are not completely clear yet, but it may be due to lack of appropriate diagnosis, treatment and cataloging of cancer cases. Because patients seldom exhibit symptoms until an advanced stage of the disease, pancreatic cancer remains one of the most lethal malignant neoplasms that caused 432,242 new deaths in 2018 (GLOBOCAN 2018 estimates). Globally, 458,918 new cases of pancreatic cancer have been reported in 2018, and 355,317 new cases are estimated to occur until 2040. Despite advancements in the detection and management of pancreatic cancer, the 5-year survival rate still stands at 9% only. To date, the causes of pancreatic carcinoma are still insufficiently known, although certain risk factors have been identified, such as tobacco smoking, diabetes mellitus, obesity, dietary factors, alcohol abuse, age, ethnicity, family history and genetic factors, Helicobacter pylori infection, non-O blood group and chronic pancreatitis. In general population, screening of large groups is not considered useful to detect the disease at its early stage, although newer techniques and the screening of tightly targeted groups (especially of those with family history), are being evaluated. Primary prevention is considered of utmost importance. Up-to-date statistics on pancreatic cancer occurrence and outcome along with a better understanding of the etiology and identifying the causative risk factors are essential for the primary prevention of this disease.
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                Author and article information

                Contributors
                Journal
                NAR Cancer
                NAR Cancer
                narcancer
                NAR Cancer
                Oxford University Press
                2632-8674
                September 2021
                14 August 2021
                14 August 2021
                : 3
                : 3
                : zcab032
                Affiliations
                Inserm U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Université Claude Bernard Lyon 1 , Centre Léon Bérard, F-69373 Lyon Cedex 08, France
                Inserm U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Université Claude Bernard Lyon 1 , Centre Léon Bérard, F-69373 Lyon Cedex 08, France
                Institut de pathologies multi-sites des Hospices Civils de Lyon , Groupement Hospitalier Est, F-69677 Bron, France
                Inserm U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Université Claude Bernard Lyon 1 , Centre Léon Bérard, F-69373 Lyon Cedex 08, France
                Laboratoire de chimie analytique, Faculté de pharmacie de Lyon, Université de Lyon , 8 avenue Rockefeller, F-69373 Lyon, France
                Laboratoire de biochimie et de pharmaco-toxicologie , Centre hospitalier Lyon-Sud – Hospices Civils de Lyon, F-69495 Pierre Bénite, France
                Inserm U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Université Claude Bernard Lyon 1 , Centre Léon Bérard, F-69373 Lyon Cedex 08, France
                Inserm U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Université Claude Bernard Lyon 1 , Centre Léon Bérard, F-69373 Lyon Cedex 08, France
                Inserm U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Université Claude Bernard Lyon 1 , Centre Léon Bérard, F-69373 Lyon Cedex 08, France
                Inserm U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Université Claude Bernard Lyon 1 , Centre Léon Bérard, F-69373 Lyon Cedex 08, France
                Inserm U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Université Claude Bernard Lyon 1 , Centre Léon Bérard, F-69373 Lyon Cedex 08, France
                Département d’Endoscopie et de Gastroentérologie , Pavillon L, Hôpital Edouard Herriot, Hospices Civils de Lyon, F-69008 Lyon, France
                Inserm U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Université Claude Bernard Lyon 1 , Centre Léon Bérard, F-69373 Lyon Cedex 08, France
                Ecole Normale Supérieure de Lyon , F-69007 Lyon, France
                Inserm U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Université Claude Bernard Lyon 1 , Centre Léon Bérard, F-69373 Lyon Cedex 08, France
                Laboratoire de biochimie et de pharmaco-toxicologie , Centre hospitalier Lyon-Sud – Hospices Civils de Lyon, F-69495 Pierre Bénite, France
                Laboratoire de toxicologie, Faculté de pharmacie de Lyon, Université de Lyon , 8 avenue Rockefeller, F-69373 Lyon, France
                Inserm U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Université Claude Bernard Lyon 1 , Centre Léon Bérard, F-69373 Lyon Cedex 08, France
                Inserm U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Université de Lyon, Université Claude Bernard Lyon 1 , Centre Léon Bérard, F-69373 Lyon Cedex 08, France
                Author notes
                To whom correspondence should be addressed. Tel: +33 478 782 819; Email: jean-jacques.diaz@ 123456lyon.unicancer.fr
                Correspondence may also be addressed to Nicole Dalla Venezia. Tel: +33 426 556 745; Email: nicole.dalla-venezia@ 123456lyon.unicancer.fr

                The authors wish it to be known that, in their opinion, the first two authors should be regarded as Joint First Authors.

                Author information
                https://orcid.org/0000-0002-9557-8221
                https://orcid.org/0000-0002-7914-4319
                Article
                zcab032
                10.1093/narcan/zcab032
                8364333
                34409299
                5972b430-2d47-458c-aa14-9e44714a724f
                © The Author(s) 2021. Published by Oxford University Press on behalf of NAR Cancer.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@ 123456oup.com

                History
                : 09 August 2021
                : 01 July 2021
                : 18 March 2021
                Page count
                Pages: 13
                Funding
                Funded by: Institut National de la Santé et de la Recherche Médicale, DOI 10.13039/501100001677;
                Funded by: Centre National de la Recherche Scientifique, DOI 10.13039/501100004794;
                Funded by: Université Claude Bernard Lyon 1, DOI 10.13039/501100006687;
                Funded by: Agence Nationale de la Recherche, DOI 10.13039/501100001665;
                Award ID: ANR-13-BSV8-0012-01 RIBOMETH
                Award ID: ANR-19-CE12-0004 ACTIMETH
                Funded by: Institut National Du Cancer, DOI 10.13039/501100006364;
                Award ID: PLBIO 2018-131 FluoRib
                Funded by: PAIR Sein program;
                Award ID: ARC INCa LNCC 7625 RiboTEM
                Funded by: SIRIC program;
                Award ID: INCa-DGOS-Inserm 12563 LYriCAN
                Funded by: Labex, DOI 10.13039/501100004100;
                Award ID: DEVCAN2UMAN
                Funded by: Fondation ARC pour la Recherche sur le Cancer, DOI 10.13039/501100004097;
                Award ID: 20161204686 MARACAS
                Funded by: Ligue Contre le Cancer, DOI 10.13039/501100004099;
                Categories
                AcademicSubjects/SCI00030
                AcademicSubjects/SCI00980
                AcademicSubjects/SCI01060
                AcademicSubjects/SCI01140
                AcademicSubjects/SCI01180
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