摘要
disintegrin和metalloprotease(亚当)17 sheddase,能够释放ectodomains膜蛋白,如生长因子(如表皮生长因子受体配体),细胞因子及其受体、粘附和信号分子。这些活动调节多种生理和病理过程包括炎症、肿瘤的生长和转移过程。在本文中,我们将总结ADAM17生物学和关注它在癌症中的作用和可能的使用ADAM17抑制剂在癌症治疗。最近的成就在这一领域的发展包括小分子metalloprotease ADAM17与增强特异性抑制剂,单克隆抗体,合成短RNA分子基因沉默。这些方法成功地抑制癌细胞的生长和侵袭性或致敏细胞毒性药物,电离辐射或靶向治疗,在临床前研究。这些发现表明ADAM17抑制剂的重新定位,这还没有被证明失败作为抗炎剂,为新的抗癌治疗的发展,尤其是在EGFR ligand-dependent癌症。未来的研究应该解决ADAM17抑制剂作为短期治疗结合不同的抗癌疗法。
关键词: ADAM17、癌症、小分子抑制剂
图形摘要
Current Drug Targets
Title:Targeting ADAM17 Sheddase Activity in Cancer
Volume: 17 Issue: 16
Author(s): Armando Rossello, Elisa Nuti, Silvano Ferrini, Marina Fabbi
Affiliation:
关键词: ADAM17、癌症、小分子抑制剂
摘要: A disintegrin and metalloprotease (ADAM)17 is a sheddase, capable of releasing the ectodomains of membrane proteins such as growth factors (e.g. Epidermal Growth Factor Receptor ligands), cytokines and their receptors, adhesion and signaling molecules. These activities regulate several physiological and pathological processes including inflammation, tumor growth and metastatic progression. In this review, we will summarize ADAM17 biology and focus on its role in cancer and the possible usage of ADAM17 inhibitors in cancer therapy. Recent achievements in this area include the development of small molecule metalloprotease inhibitors with enhanced specificity for ADAM17, monoclonal antibodies, and synthetic short RNA molecules for gene silencing. These approaches successfully inhibited cancer cell growth and invasiveness or sensitized them to cytotoxic drugs, ionizing radiations or targeted therapies, in preclinical studies. These findings suggest the repositioning of ADAM17 inhibitors, which have yet proven unsuccessful as anti-inflammatory agents, for the development of new anti-cancer therapies, particularly in EGFR ligand-dependent cancers. Future studies should address ADAM17 inhibitors as short-term treatments in combination with different anti-cancer therapies.
Export Options
About this article
Cite this article as:
Armando Rossello, Elisa Nuti, Silvano Ferrini, Marina Fabbi , Targeting ADAM17 Sheddase Activity in Cancer, Current Drug Targets 2016; 17 (16) . https://dx.doi.org/10.2174/1389450117666160727143618
DOI https://dx.doi.org/10.2174/1389450117666160727143618 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
Related Journals
Related Books
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers
Related Articles
-
Women Tipping the Scale During Pregnancy: A Special Population for Obesity Interventions,Treatments and Clinical Trials
Current Pharmaceutical Design Synthesis and Biological Evaluation of the Salicylamide and Salicylic Acid Derivatives as Anti-Estrogen Agents
Medicinal Chemistry Proteasome Regulators: Activators and Inhibitors
Current Medicinal Chemistry Effect of Pinocembrin Isolated from Boesenbergia pandurata on Xenobiotic-Metabolizing Enzymes in Rat Liver
Drug Metabolism Letters Linking Fold, Function and Phylogeny: A Comparative Genomics View on Protein (Domain) Evolution
Current Genomics Synthesis and Antibacterial / Anticancer Activities of Compounds Containing Pyrazole Ring Linked to Piperazines
Current Bioactive Compounds Puerarin Stimulates Osteogenic Differentiation and Bone Formation Through the ERK1/2 and p38-MAPK Signaling Pathways
Current Molecular Medicine MicroRNA Gene Networks in Oncogenesis
Current Genomics The Anticancer Activity of the N-Terminal CARD-Like Domain of Arginine Deiminase (ADI) from Pseudomonas aeruginosa
Letters in Drug Design & Discovery Electrochemical Immunosensors for Disease Detection and Diagnosis
Current Medicinal Chemistry Editorial (Thematic Issue: Combined Cancer Therapy)
Current Pharmaceutical Design Alternate Strategies of Hsp90 Modulation for the Treatment of Cancer and Other Diseases
Current Topics in Medicinal Chemistry The Synthetic Oleanane Triterpenoid HIMOXOL Induces Autophagy in Breast Cancer Cells via ERK1/2 MAPK Pathway and Beclin-1 Up-regulation
Anti-Cancer Agents in Medicinal Chemistry Proteins as Alternate Targets of Enediynes
Letters in Drug Design & Discovery Role of EGFR Inhibitors in the Treatment of Central Nervous System Metastases from Non-Small Cell Lung Cancer
Current Cancer Drug Targets Adverse Effects and Safety of Etirinotecan Pegol, a Novel Topoisomerase Inhibitor, in Cancer Treatment: A Systematic Review
Current Cancer Therapy Reviews Evaluation of Cytotoxic Mechanisms of Clinacanthus Nutans Extracts in Cancer Cells
The Natural Products Journal Novel Substituted Quinazolines for Potent EGFR Tyrosine Kinase Inhibitors
Current Medicinal Chemistry Saponins: the Potential Chemotherapeutic Agents in Pursuing New Anti-glioblastoma Drugs
Mini-Reviews in Medicinal Chemistry Promises and Challenges of Adult Stem Cells in Cancer Therapy
Immunology, Endocrine & Metabolic Agents in Medicinal Chemistry (Discontinued)