29
views
0
recommends
+1 Recommend
4 collections
    0
    shares

          The flagship journal of the Society for Endocrinology. Learn more

      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      ENDOCRINOLOGY IN THE TIME OF COVID-19: Clinical management of neuroendocrine neoplasms (NENs)

      other

      Read this article at

      ScienceOpenPublisherPMC
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          In viral pandemics, most specifically Covid-19, many patients with neuroendocrine neoplasms (NENs), including phaeochromocytomas, paragangliomas and medullary thyroid carcinoma, may develop Covid-19 in a mild or severe form, or be concerned about the influence of viral infection relative to their anti-tumoral therapy. In general, newly presenting patients should be assessed, and patients recently receiving chemotherapy, targeted therapy or radionuclide therapy, or showing tumour growth, should be closely followed. For previously diagnosed patients, who have indolent disease, some delay in routine follow-up or treatment may not be problematic. However, patients developing acute secretory syndromes due to functional neuroendocrine neoplasms (such as of the pancreas, intestine or lung), phaeochromocytomas and paragangliomas, will require prompt treatment. Patients with life-threatening Covid-19-related symptoms should be urgently treated and long-term anti-tumoral treatments may be temporarily delayed. In patients with especially aggressive NENs, a careful judgement should be made regarding the severity of any Covid-19 illness, tumour grade, and the immunosuppressant effects of any planned chemotherapy, immunotherapy (e.g. interferon-alpha), targeted therapy or related treatment. In other cases, especially patients with completely resected NENs, or who are under surveillance for a genetic disorder, a telephone or delayed consultation may be in order, balancing the risk of a delay against that of the possible development of Covid-19.

          Related collections

          Most cited references22

          • Record: found
          • Abstract: found
          • Article: not found

          SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor

          Summary The recent emergence of the novel, pathogenic SARS-coronavirus 2 (SARS-CoV-2) in China and its rapid national and international spread pose a global health emergency. Cell entry of coronaviruses depends on binding of the viral spike (S) proteins to cellular receptors and on S protein priming by host cell proteases. Unravelling which cellular factors are used by SARS-CoV-2 for entry might provide insights into viral transmission and reveal therapeutic targets. Here, we demonstrate that SARS-CoV-2 uses the SARS-CoV receptor ACE2 for entry and the serine protease TMPRSS2 for S protein priming. A TMPRSS2 inhibitor approved for clinical use blocked entry and might constitute a treatment option. Finally, we show that the sera from convalescent SARS patients cross-neutralized SARS-2-S-driven entry. Our results reveal important commonalities between SARS-CoV-2 and SARS-CoV infection and identify a potential target for antiviral intervention.
            • Record: found
            • Abstract: found
            • Article: not found

            Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus

            Spike (S) proteins of coronaviruses, including the coronavirus that causes severe acute respiratory syndrome (SARS), associate with cellular receptors to mediate infection of their target cells 1,2 . Here we identify a metallopeptidase, angiotensin-converting enzyme 2 (ACE2) 3,4 , isolated from SARS coronavirus (SARS-CoV)-permissive Vero E6 cells, that efficiently binds the S1 domain of the SARS-CoV S protein. We found that a soluble form of ACE2, but not of the related enzyme ACE1, blocked association of the S1 domain with Vero E6 cells. 293T cells transfected with ACE2, but not those transfected with human immunodeficiency virus-1 receptors, formed multinucleated syncytia with cells expressing S protein. Furthermore, SARS-CoV replicated efficiently on ACE2-transfected but not mock-transfected 293T cells. Finally, anti-ACE2 but not anti-ACE1 antibody blocked viral replication on Vero E6 cells. Together our data indicate that ACE2 is a functional receptor for SARS-CoV. Supplementary information The online version of this article (doi:10.1038/nature02145) contains supplementary material, which is available to authorized users.
              • Record: found
              • Abstract: found
              • Article: not found

              High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study

              Little evidence of increased thrombotic risk is available in COVID-19 patients. Our purpose was to assess thrombotic risk in severe forms of SARS-CoV-2 infection.

                Author and article information

                Journal
                Eur J Endocrinol
                Eur J Endocrinol
                EJE
                European Journal of Endocrinology
                Bioscientifica Ltd (Bristol )
                0804-4643
                1479-683X
                August 2020
                09 June 2020
                : 183
                : 2
                : G79-G88
                Affiliations
                [1 ]Wolfson Diabetes and Endocrinology Clinic , Cambridge University Hospital NHS Foundation Trust, Cambridge, UK
                [2 ]Department of Medical Genetics , Cambridge University, Cambridge, UK
                [3 ]Department of Endocrine Oncology , University Medical Centre Utrecht, ENETS Centre of Excellence, Utrecht, Netherlands
                [4 ]Division of Endocrinology , Abdominal Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland
                [5 ]Royal Free Hospital ENETs Centre of Excellence , London, UK
                [6 ]Centre for Endocrinology , Barts and the London School of Medicine, London, UK
                [7 ]Oxford Centre for Diabetes , Endocrinology and Metabolism, University of Oxford, Oxford, UK
                [8 ]Academic Endocrine Unit , Radcliffe Department of Medicine, University of Oxford, Oxford, UK
                Author notes
                Correspondence should be addressed to R V Thakker; Email: rajesh.thakker@ 123456ndm.ox.ac.uk

                This manuscript is part of a commissioned series of urgent clinical guidance documents on the management of endocrine conditions in the time of Covid-19. This clinical guidance document underwent expedited open peer review by Karel Pacak (NICHD, Bethesdad, MD, USA), Simona Grozinsky-Glasberg (Hadassah-Hebrew University Hospital, Jerusalem, Israel), and Wouter de Herder (Erasmus MC, Rotterdam, The Netherlands)

                Article
                EJE-20-0424
                10.1530/EJE-20-0424
                7938008
                32554825
                714ad1cb-d36f-48bd-96ec-84d4b7e496f1
                © 2020 The authors

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 25 April 2020
                : 09 June 2020
                Categories
                Clinical Practice Guidance

                Endocrinology & Diabetes
                Endocrinology & Diabetes

                Comments

                Comment on this article

                Related Documents Log