706
views
0
recommends
+1 Recommend
2 collections
    4
    shares

      To submit to Bentham Journals, please click here

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

      Reduction of Breast Cancer Relapses with Perioperative Non-Steroidal Anti-Inflammatory Drugs: New Findings and a Review

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          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

          To explain a bimodal pattern of hazard of relapse among early stage breast cancer patients identified in multiple databases, we proposed that late relapses result from steady stochastic progressions from single dormant malignant cells to avascular micrometastases and then on to growing deposits. However in order to explain early relapses, we had to postulate that something happens at about the time of surgery to provoke sudden exits from dormant phases to active growth and then to detection. Most relapses in breast cancer are in the early category. Recent data from Forget et al. suggest an unexpected mechanism. They retrospectively studied results from 327 consecutive breast cancer patients comparing various perioperative analgesics and anesthetics in one Belgian hospital and one surgeon. Patients were treated with mastectomy and conventional adjuvant therapy. Relapse hazard updated Sept 2011 are presented. A common Non-Steroidal Anti-Inflammatory Drug (NSAID) analgesic used in surgery produced far superior disease-free survival in the first 5 years after surgery. The expected prominent early relapse events in months 9-18 are reduced 5-fold. If this observation holds up to further scrutiny, it could mean that the simple use of this safe, inexpensive and effective anti-inflammatory agent at surgery might eliminate early relapses. Transient systemic inflammation accompanying surgery could facilitate angiogenesis of dormant micrometastases, proliferation of dormant single cells, and seeding of circulating cancer stem cells (perhaps in part released from bone marrow) resulting in early relapse and could have been effectively blocked by the perioperative anti-inflammatory agent.

          Related collections

          Most cited references109

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

          Inflammation and cancer.

          Recent data have expanded the concept that inflammation is a critical component of tumour progression. Many cancers arise from sites of infection, chronic irritation and inflammation. It is now becoming clear that the tumour microenvironment, which is largely orchestrated by inflammatory cells, is an indispensable participant in the neoplastic process, fostering proliferation, survival and migration. In addition, tumour cells have co-opted some of the signalling molecules of the innate immune system, such as selectins, chemokines and their receptors for invasion, migration and metastasis. These insights are fostering new anti-inflammatory therapeutic approaches to cancer development.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Inflammation and cancer: back to Virchow?

            The response of the body to a cancer is not a unique mechanism but has many parallels with inflammation and wound healing. This article reviews the links between cancer and inflammation and discusses the implications of these links for cancer prevention and treatment. We suggest that the inflammatory cells and cytokines found in tumours are more likely to contribute to tumour growth, progression, and immunosuppression than they are to mount an effective host antitumour response. Moreover cancer susceptibility and severity may be associated with functional polymorphisms of inflammatory cytokine genes, and deletion or inhibition of inflammatory cytokines inhibits development of experimental cancer. If genetic damage is the "match that lights the fire" of cancer, some types of inflammation may provide the "fuel that feeds the flames". Over the past ten years information about the cytokine and chemokine network has led to development of a range of cytokine/chemokine antagonists targeted at inflammatory and allergic diseases. The first of these to enter the clinic, tumour necrosis factor antagonists, have shown encouraging efficacy. In this article we have provided a rationale for the use of cytokine and chemokine blockade, and further investigation of non-steroidal anti-inflammatory drugs, in the chemoprevention and treatment of malignant diseases.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Deterministic Nonperiodic Flow

                Bookmark

                Author and article information

                Journal
                Curr Med Chem
                Curr. Med. Chem
                CMC
                Current Medicinal Chemistry
                Bentham Science Publishers
                0929-8673
                1875-533X
                November 2013
                November 2013
                : 20
                : 33
                : 4163-4176
                Affiliations
                [1 ]Harvard School of Public Health, BLDG I, Rm 1311, 665 Huntington, Ave, Boston, MA 02115, USA;
                [2 ]Royal Free and UCL Medical School, Centre for Clinical Science and Technology, University College London, Clerkenwell Building, Archway Campus, Highgate Hill, London, UK;
                [3 ]Scientific Directorate, Fondazione IRCCS Istituto Nazionale Tumori, Via Venezian 1, 20133 Milan, Italy;
                [4 ]Oncology Analytics, Inc, 8751 W. Broward Blvd, Suite 500, Plantation FL 33324, USA;
                [5 ]Department of Anesthesiology, Universite Catholique de Louvain, St-Luc Hospital, av. Hippocrate 10-1821, 1200 Brussels, Belgium;
                [6 ]James Paget University Hospital, Lowestoft Road, Gorleston, Great Yarmouth, Norfolk NR31 6LA, UK;
                [7 ]Clinical Trials Group of the Division of Surgery and Interventional Science, University College London, Clerkenwell Building, Archway Campus, Highgate Hill, London N19 5LW, UK;
                [8 ]Beth Israel Deaconess Medical Center, 330 Brookline Ave, Boston, MA 02215, Harvard Medical School, and GlobalCures, Boston, MA 02115, USA
                Author notes
                [* ]Address correspondence to this author at the Harvard School of Public Health, BLDG I, Rm 1311, 665 Huntington, Ave, Boston, MA 02115, USA; Tel: 1-203-675-0017; Fax: 1-617-432-4310; Email: michael.retsky@ 123456gmail.com
                Article
                CMC-20-4163
                10.2174/09298673113209990250
                3831877
                23992307
                6af44dcd-6af1-496e-90dc-1d4ad1bd54e1
                © 2013 Bentham Science Publishers

                This is an open access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.5/), which permits unrestrictive use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 17 February 2013
                : 26 March 2013
                : 31 March 2013
                Categories
                Article

                Pharmaceutical chemistry
                breast cancer,early relapse,late relapse,angiogenesis,inflammation,surgery,analgesic,perioperative,metastases,bleeding,nsaid,dormancy.

                Comments

                Comment on this article