Literature DB >> 20303610

Inhibition of multifunctional dipeptidyl peptidase-IV: is there a risk of oncological and immunological adverse effects?

Tomas Stulc1, Aleksi Sedo.   

Abstract

Inhibitors of dipeptidyl peptidase-IV (DPP-IV) are a novel class of anti-diabetes drugs; inhibiting the breakdown of incretins, they increase their biological availability and decrease thus blood glucose levels. However, in addition to regulating glucose homeostasis, DPP-IV has many diverse functions, such as modulating cell growth, differentiation and transformation and immune function. Within the immune system, DPP-IV exerts mainly stimulating effects, while its relation to malignancies is highly variable. Therefore, long-term inhibition of this enzyme could have serious side effects including immune dysregulation or increased risk of cancer. Although the data on the effects of DPP-IV inhibitors in humans are scarce, the increased risk of infections and the tendency towards a higher incidence of some tumours fall in line with experimental evidence suggesting the possibility of their adverse immunological and oncological effects. Further research is obviously needed to clarify the effector mechanisms of DPP-IV inhibitors on immune function and tumour biology. Most important, however, is obtaining reassuring safety data from adequately powered, long-term trials of DPP-IV inhibitors in humans. In the meantime, all the potential risks of DPP-IV inhibitors should be kept in mind, and this class of drugs needs to be regarded with some degree of caution. Copyright 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 20303610     DOI: 10.1016/j.diabres.2010.02.017

Source DB:  PubMed          Journal:  Diabetes Res Clin Pract        ISSN: 0168-8227            Impact factor:   5.602


  15 in total

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2.  Pancreatitis, pancreatic, and thyroid cancer with glucagon-like peptide-1-based therapies.

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3.  Exenatide therapy and the risk of pancreatitis and pancreatic cancer in a privately insured population.

Authors:  John A Romley; Dana P Goldman; Matthew Solomon; Daniel McFadden; Anne L Peters
Journal:  Diabetes Technol Ther       Date:  2012-07-30       Impact factor: 6.118

4.  Effect of zinc and calcium ions on the rat kidney membrane-bound form of dipeptidyl peptidase IV.

Authors:  Hansel Gómez; Mae Chappé; Pedro A Valiente; Tirso Pons; María de Los Angeles Chávez; Jean-Louis Charli; Isel Pascual
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5.  DPP4 inhibitor-induced polyarthritis: a report of three cases.

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6.  Cancer risk in type 2 diabetes mellitus: metabolic links and therapeutic considerations.

Authors:  Grace Sun; Sangeeta R Kashyap
Journal:  J Nutr Metab       Date:  2011-06-01

Review 7.  Recent Advances in Dipeptidyl-Peptidase-4 Inhibition Therapy: Lessons from the Bench and Clinical Trials.

Authors:  Jixin Zhong; Quan Gong; Aditya Goud; Srividya Srinivasamaharaj; Sanjay Rajagopalan
Journal:  J Diabetes Res       Date:  2015-05-14       Impact factor: 4.011

Review 8.  The Dipeptidyl Peptidase Family, Prolyl Oligopeptidase, and Prolyl Carboxypeptidase in the Immune System and Inflammatory Disease, Including Atherosclerosis.

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Review 9.  Diabetes and cancer: two diseases with obesity as a common risk factor.

Authors:  S K Garg; H Maurer; K Reed; R Selagamsetty
Journal:  Diabetes Obes Metab       Date:  2013-06-12       Impact factor: 6.577

10.  Prognostic significance of the combined expression of neutral endopeptidase and dipeptidyl peptidase IV in intrahepatic cholangiocarcinoma patients after surgery resection.

Authors:  Jianyong Zhu; Xiaodong Guo; Baoan Qiu; Zhiyan Li; Nianxin Xia; Yingxiang Yang; Peng Liu
Journal:  Onco Targets Ther       Date:  2014-02-17       Impact factor: 4.147

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