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      Targeting autophagy in prostate cancer: preclinical and clinical evidence for therapeutic response

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          Abstract

          Prostate cancer is a leading cause of death worldwide and new estimates revealed prostate cancer as the leading cause of death in men in 2021. Therefore, new strategies are pertinent in the treatment of this malignant disease. Macroautophagy/autophagy is a “self-degradation” mechanism capable of facilitating the turnover of long-lived and toxic macromolecules and organelles. Recently, attention has been drawn towards the role of autophagy in cancer and how its modulation provides effective cancer therapy. In the present review, we provide a mechanistic discussion of autophagy in prostate cancer. Autophagy can promote/inhibit proliferation and survival of prostate cancer cells. Besides, metastasis of prostate cancer cells is affected (via induction and inhibition) by autophagy. Autophagy can affect the response of prostate cancer cells to therapy such as chemotherapy and radiotherapy, given the close association between autophagy and apoptosis. Increasing evidence has demonstrated that upstream mediators such as AMPK, non-coding RNAs, KLF5, MTOR and others regulate autophagy in prostate cancer. Anti-tumor compounds, for instance phytochemicals, dually inhibit or induce autophagy in prostate cancer therapy. For improving prostate cancer therapy, nanotherapeutics such as chitosan nanoparticles have been developed. With respect to the context-dependent role of autophagy in prostate cancer, genetic tools such as siRNA and CRISPR-Cas9 can be utilized for targeting autophagic genes. Finally, these findings can be translated into preclinical and clinical studies to improve survival and prognosis of prostate cancer patients.

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          Highlights

          • Prostate cancer is among the leading causes of death in men where targeting autophagy is of importance in treatment;

          • Autophagy governs proliferation and metastasis capacity of prostate cancer cells;

          • Autophagy modulation is of interest in improving the therapeutic response of prostate cancer cells;

          • Molecular pathways, especially involving non-coding RNAs, regulate autophagy in prostate cancer;

          • Autophagy possesses both diagnostic and prognostic roles in prostate cancer, with promises for clinical application.

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          Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries

          This article provides an update on the global cancer burden using the GLOBOCAN 2020 estimates of cancer incidence and mortality produced by the International Agency for Research on Cancer. Worldwide, an estimated 19.3 million new cancer cases (18.1 million excluding nonmelanoma skin cancer) and almost 10.0 million cancer deaths (9.9 million excluding nonmelanoma skin cancer) occurred in 2020. Female breast cancer has surpassed lung cancer as the most commonly diagnosed cancer, with an estimated 2.3 million new cases (11.7%), followed by lung (11.4%), colorectal (10.0 %), prostate (7.3%), and stomach (5.6%) cancers. Lung cancer remained the leading cause of cancer death, with an estimated 1.8 million deaths (18%), followed by colorectal (9.4%), liver (8.3%), stomach (7.7%), and female breast (6.9%) cancers. Overall incidence was from 2-fold to 3-fold higher in transitioned versus transitioning countries for both sexes, whereas mortality varied <2-fold for men and little for women. Death rates for female breast and cervical cancers, however, were considerably higher in transitioning versus transitioned countries (15.0 vs 12.8 per 100,000 and 12.4 vs 5.2 per 100,000, respectively). The global cancer burden is expected to be 28.4 million cases in 2040, a 47% rise from 2020, with a larger increase in transitioning (64% to 95%) versus transitioned (32% to 56%) countries due to demographic changes, although this may be further exacerbated by increasing risk factors associated with globalization and a growing economy. Efforts to build a sustainable infrastructure for the dissemination of cancer prevention measures and provision of cancer care in transitioning countries is critical for global cancer control.
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            Cancer Statistics, 2021

            Each year, the American Cancer Society estimates the numbers of new cancer cases and deaths in the United States and compiles the most recent data on population-based cancer occurrence. Incidence data (through 2017) were collected by the Surveillance, Epidemiology, and End Results Program; the National Program of Cancer Registries; and the North American Association of Central Cancer Registries. Mortality data (through 2018) were collected by the National Center for Health Statistics. In 2021, 1,898,160 new cancer cases and 608,570 cancer deaths are projected to occur in the United States. After increasing for most of the 20th century, the cancer death rate has fallen continuously from its peak in 1991 through 2018, for a total decline of 31%, because of reductions in smoking and improvements in early detection and treatment. This translates to 3.2 million fewer cancer deaths than would have occurred if peak rates had persisted. Long-term declines in mortality for the 4 leading cancers have halted for prostate cancer and slowed for breast and colorectal cancers, but accelerated for lung cancer, which accounted for almost one-half of the total mortality decline from 2014 to 2018. The pace of the annual decline in lung cancer mortality doubled from 3.1% during 2009 through 2013 to 5.5% during 2014 through 2018 in men, from 1.8% to 4.4% in women, and from 2.4% to 5% overall. This trend coincides with steady declines in incidence (2.2%-2.3%) but rapid gains in survival specifically for nonsmall cell lung cancer (NSCLC). For example, NSCLC 2-year relative survival increased from 34% for persons diagnosed during 2009 through 2010 to 42% during 2015 through 2016, including absolute increases of 5% to 6% for every stage of diagnosis; survival for small cell lung cancer remained at 14% to 15%. Improved treatment accelerated progress against lung cancer and drove a record drop in overall cancer mortality, despite slowing momentum for other common cancers.
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              MicroRNAs: target recognition and regulatory functions.

              MicroRNAs (miRNAs) are endogenous approximately 23 nt RNAs that play important gene-regulatory roles in animals and plants by pairing to the mRNAs of protein-coding genes to direct their posttranscriptional repression. This review outlines the current understanding of miRNA target recognition in animals and discusses the widespread impact of miRNAs on both the expression and evolution of protein-coding genes.
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                Author and article information

                Contributors
                milad.ashrafizadeh@sabanciuniv.edu
                apkumar@nus.edu.sg
                ywang@bccrc.ca
                Journal
                J Exp Clin Cancer Res
                J Exp Clin Cancer Res
                Journal of Experimental & Clinical Cancer Research : CR
                BioMed Central (London )
                0392-9078
                1756-9966
                22 March 2022
                22 March 2022
                2022
                : 41
                : 105
                Affiliations
                [1 ]GRID grid.5334.1, ISNI 0000 0004 0637 1566, Faculty of Engineering and Natural Sciences, , Sabanci University, ; Orta Mahalle, Üniversite Caddesi No. 27, Orhanlı, Tuzla, 34956 Istanbul, Turkey
                [2 ]GRID grid.411463.5, ISNI 0000 0001 0706 2472, Department of Genetics, Faculty of Advanced Science and Technology, Tehran Medical Sciences, , Islamic Azad University, ; Tehran, Iran
                [3 ]GRID grid.411463.5, ISNI 0000 0001 0706 2472, Farhikhtegan Medical Convergence sciences Research Center, Farhikhtegan Hospital Tehran Medical sciences, , Islamic Azad University, ; Tehran, Iran
                [4 ]GRID grid.472472.0, ISNI 0000 0004 1756 1816, Department of Biology, Faculty of Science, , Islamic Azad University, Science and Research Branch, ; Tehran, Iran
                [5 ]GRID grid.472315.6, ISNI 0000 0004 0494 0825, Faculty of Veterinary Medicine, Kazerun Branch, , Islamic Azad University, ; Kazerun, Iran
                [6 ]GRID grid.508740.e, ISNI 0000 0004 5936 1556, Department of Biomedical Engineering, Faculty of Engineering and Natural Sciences, , Istinye University, ; 34396 Istanbul, Turkey
                [7 ]GRID grid.46072.37, ISNI 0000 0004 0612 7950, Department of Comparative Biosciences, Faculty of Veterinary Medicine, , University of Tehran, ; Tehran, 1417466191 Iran
                [8 ]GRID grid.46072.37, ISNI 0000 0004 0612 7950, Department of Food Hygiene and Quality Control, Division of Epidemiology & Zoonoses, , Faculty of Veterinary Medicine University of Tehran, ; Tehran, Iran
                [9 ]GRID grid.17091.3e, ISNI 0000 0001 2288 9830, Department of Urological Sciences and Vancouver Prostate Centre, , University of British Columbia, ; V6H3Z6, Vancouver, BC Canada
                [10 ]GRID grid.10837.3d, ISNI 0000 0000 9606 9301, Cancer Research Group-School of Life Health and Chemical Sciences, , The Open University, ; Walton Hall, Milton Keynes, MK7 6AA UK
                [11 ]GRID grid.34477.33, ISNI 0000000122986657, Department of Laboratory Medicine and Pathology, , University of Washington, ; Seattle, WA 98195 USA
                [12 ]GRID grid.8547.e, ISNI 0000 0001 0125 2443, Shanghai Institute of Cardiovascular Diseases, Department of Cardiology, Zhongshan Hospital, , Fudan University, ; Shanghai, 200032 China
                [13 ]GRID grid.214458.e, ISNI 0000000086837370, Life Sciences Institute & Department of Molecular, Cellular and Developmental Biology, , University of Michigan, ; Ann Arbor, MI 48109 USA
                [14 ]GRID grid.4280.e, ISNI 0000 0001 2180 6431, Cancer Science Institute of Singapore and Department of Pharmacology, Yong Loo Lin School of Medicine, , National University of Singapore, ; Singapore, 117599 Singapore
                [15 ]GRID grid.4280.e, ISNI 0000 0001 2180 6431, NUS Centre for Cancer Research (N2CR), Yong Loo Lin School of Medicine, , National University of Singapore, ; Singapore, Singapore
                Author information
                http://orcid.org/0000-0003-0391-1769
                http://orcid.org/0000-0002-0275-0783
                http://orcid.org/0000-0002-7828-8118
                http://orcid.org/0000-0002-3754-5712
                http://orcid.org/0000-0002-9749-8591
                Article
                2293
                10.1186/s13046-022-02293-6
                8939209
                35317831
                8accd6b7-1c04-4e75-85e5-bec094b569cd
                © The Author(s) 2022

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 12 December 2021
                : 16 February 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001459, Ministry of Education - Singapore;
                Award ID: MOE-T2EP30120-0016
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100002655, Terry Fox Foundation;
                Award ID: 1062
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100000024, Canadian Institutes of Health Research;
                Award ID: 141635
                Award Recipient :
                Categories
                Review
                Custom metadata
                © The Author(s) 2022

                Oncology & Radiotherapy
                anti-tumor compounds,autophagy,biomarker,non-coding rnas,prostate cancer,therapy response

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