Literature DB >> 34259137

Use of Exogenous Enzymes in Human Therapy: Approved Drugs and Potential Applications.

Patrizia Cioni1, Edi Gabellieri1, Barbara Campanini2, Stefano Bettati1, Samanta Raboni1.   

Abstract

The development of safe and efficacious enzyme-based human therapies has increased greatly in the last decades, thanks to remarkable advances in the understanding of the molecular mechanisms responsible for different diseases, and the characterization of the catalytic activity of relevant exogenous enzymes that may play a remedial effect in the treatment of such pathologies. Several enzyme-based biotherapeutics have been approved by FDA (the U.S. Food and Drug Administration) and EMA (the European Medicines Agency) and many are undergoing clinical trials. Apart from enzyme replacement therapy in human genetic diseases, which is not discussed in this review, approved enzymes for human therapy find applications in several fields, from cancer therapy to thrombolysis and the treatment, e.g., of clotting disorders, cystic fibrosis, lactose intolerance and collagen-based disorders. The majority of therapeutic enzymes are of microbial origin, the most convenient source due to fast, simple and cost-effective production and manipulation. The use of microbial recombinant enzymes has broadened prospects for human therapy but some hurdles such as high immunogenicity, protein instability, short half-life and low substrate affinity, still need to be tackled. Alternative sources of enzymes, with reduced side effects and improved activity, as well as genetic modification of the enzymes and novel delivery systems are constantly searched. Chemical modification strategies, targeted-and/or nanocarrier-mediated delivery, directed evolution and site-specific mutagenesis, fusion proteins generated by genetic manipulation are the most explored tools to reduce toxicity and improve bioavailability and cellular targeting. This review provides a description of exogenous enzymes that are presently employed for the therapeutic management of human diseases with their current FDA/EMA-approved status, along with those already experimented at the clinical level and potential promising candidates. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Entities:  

Keywords:  Recombinant proteins; anticancer biologics; biopharmaceuticals.; cancer enzymatic starvation; fibrinolytic therapy; pharmaceutical enzymes

Mesh:

Substances:

Year:  2022        PMID: 34259137     DOI: 10.2174/0929867328666210713094722

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  2 in total

Review 1.  Harnessing the Potential of Enzymes as Inhaled Therapeutics in Respiratory Tract Diseases: A Review of the Literature.

Authors:  Gilles Vanderstocken; Nicholas L Woolf; Giuseppe Trigiante; Jessica Jackson; Rory McGoldrick
Journal:  Biomedicines       Date:  2022-06-17

2.  A Key Silencing Histone Mark on Chromatin Is Lost When Colorectal Adenocarcinoma Cells Are Depleted of Methionine by Methionine γ-Lyase.

Authors:  Samanta Raboni; Serena Montalbano; Stephanie Stransky; Benjamin A Garcia; Annamaria Buschini; Stefano Bettati; Simone Sidoli; Andrea Mozzarelli
Journal:  Front Mol Biosci       Date:  2021-10-01
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.