Chemokines as novel therapeutic targets in inflammatory diseases

2002 ◽  
Vol 63 (7) ◽  
pp. 1191-1196 ◽  
Author(s):  
Maureen N. Ajuebor ◽  
Mark G. Swain ◽  
Mauro Perretti
2017 ◽  
Author(s):  
Charlotte Lussey-Lepoutre ◽  
Kate E R Hollinshead ◽  
Christian Ludwig ◽  
Melanie Menara ◽  
Aurelie Morin ◽  
...  

2013 ◽  
Vol 20 (37) ◽  
pp. 4806-4814 ◽  
Author(s):  
Brigitta Buttari ◽  
Elisabetta Profumo ◽  
Rita Businaro ◽  
Luciano Saso ◽  
Raffaele Capoano ◽  
...  

2016 ◽  
Vol 16 (20) ◽  
pp. 2303-2315 ◽  
Author(s):  
Rajender Kumar ◽  
Parvati Sharma ◽  
Deepak Kumar Gaur ◽  
Shikha Jain

Cancers ◽  
2021 ◽  
Vol 13 (8) ◽  
pp. 1781
Author(s):  
Gustavo A. Arias-Pinilla ◽  
Helmout Modjtahedi

Pancreatic cancer remains as one of the most aggressive cancer types. In the absence of reliable biomarkers for its early detection and more effective therapeutic interventions, pancreatic cancer is projected to become the second leading cause of cancer death in the Western world in the next decade. Therefore, it is essential to discover novel therapeutic targets and to develop more effective and pancreatic cancer-specific therapeutic agents. To date, 45 monoclonal antibodies (mAbs) have been approved for the treatment of patients with a wide range of cancers; however, none has yet been approved for pancreatic cancer. In this comprehensive review, we discuss the FDA approved anticancer mAb-based drugs, the results of preclinical studies and clinical trials with mAbs in pancreatic cancer and the factors contributing to the poor response to antibody therapy (e.g. tumour heterogeneity, desmoplastic stroma). MAb technology is an excellent tool for studying the complex biology of pancreatic cancer, to discover novel therapeutic targets and to develop various forms of antibody-based therapeutic agents and companion diagnostic tests for the selection of patients who are more likely to benefit from such therapy. These should result in the approval and routine use of antibody-based agents for the treatment of pancreatic cancer patients in the future.


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