Proteasome inhibitors in the treatment of multiple myeloma

التفاصيل البيبلوغرافية
العنوان: Proteasome inhibitors in the treatment of multiple myeloma
المؤلفون: Jatin J. Shah, Robert Z. Orlowski
المصدر: Leukemia. 23:1964-1979
بيانات النشر: Springer Science and Business Media LLC, 2009.
سنة النشر: 2009
مصطلحات موضوعية: Oncology, Cancer Research, medicine.medical_specialty, Antineoplastic Agents, Article, Bortezomib, Lactones, chemistry.chemical_compound, Chemosensitization, hemic and lymphatic diseases, Internal medicine, medicine, Humans, Protease Inhibitors, Pyrroles, Multiple myeloma, Hematology, business.industry, medicine.disease, Boronic Acids, Carfilzomib, Proteasome, chemistry, Pyrazines, Immunology, Proteasome inhibitor, Multiple Myeloma, business, Oligopeptides, Salinosporamide A, medicine.drug
الوصف: Targeting intracellular protein turnover by inhibiting the ubiquitin-proteasome pathway as a strategy for cancer therapy is a new addition to our chemotherapeutic armamentarium, and has seen its greatest successes against multiple myeloma. The first-in-class proteasome inhibitor bortezomib was initially approved for treatment of patients in the relapsed/refractory setting as a single agent, and was recently shown to induce even greater benefits as part of rationally-designed combinations that overcome chemoresistance. Modulation of proteasome function is also a rational approach to achieve chemosensitization to other anti-myeloma agents, and bortezomib has now been incorporated into the front-line setting. Bortezomib-based induction regimens are able to achieve higher overall response rates and response qualities than was the case with prior standards of care, and unlike these older approaches, maintain efficacy in patients with clinically- and molecularly-defined high-risk disease. Second-generation proteasome inhibitors with novel properties, such as NPI-0052 and carfilzomib, are entering the clinical arena, and showing evidence of anti-myeloma activity. In this spotlight review, we provide an overview of the current state of the art use of bortezomib and other proteasome inhibitors against multiple myeloma, and highlight areas for future study that will further optimize our ability to benefit patients with this disease.
تدمد: 1476-5551
0887-6924
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70dbb635bcff79a2b7bb4d033728c302Test
https://doi.org/10.1038/leu.2009.173Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....70dbb635bcff79a2b7bb4d033728c302
قاعدة البيانات: OpenAIRE