Exosomes in the Treatment of Pancreatic Cancer: A Moonshot to PDAC Treatment?

被引:19
作者
Papadakos, Stavros P. [1 ]
Dedes, Nikolaos [1 ]
Pergaris, Alexandros [1 ]
Gazouli, Maria [2 ]
Theocharis, Stamatios [1 ]
机构
[1] Natl & Kapodistrian Univ Athens, Med Sch, Dept Pathol 1, Athens 11527, Greece
[2] Natl & Kapodistrian Univ Athens, Med Sch, Lab Biol, Athens 11527, Greece
关键词
pancreatic cancer; exosomes; biomarkers; diagnosis; prognosis; therapy; MESENCHYMAL STROMAL CELLS; DUCTAL ADENOCARCINOMA; NAB-PACLITAXEL; RISK-FACTORS; STEM-CELLS; GEMCITABINE; CHEMORESISTANCE; IMMUNOTHERAPY; ASSOCIATION; RESISTANCE;
D O I
10.3390/ijms23073620
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pancreatic Ductal Adenocarcinoma (PDAC) constitutes a leading cause of cancer death globally. Its mortality remains unaltered despite the considerable scientific progress made in the fields of diagnostics and treatment. Exosomes comprise of small extracellular vesicles secreted by nearly all cells; their cargo contains a vast array of biomolecules, such as proteins and microRNAs. It is currently established that their role as messengers is central to a plethora of both physiologic and pathologic processes. Accumulating data have shed light on their contributions to carcinogenesis, metastasis, and immunological response. Meanwhile, the advancement of personalized targeted therapies into everyday clinical practice necessitates the development of cost-efficient treatment approaches. The role of exosomes is currently being extensively investigated towards this direction. This review aims to summarize the current pre-clinical and clinical evidence regarding the effects of exosomal applications in the timely diagnosis, prognosis, and therapeutic management of pancreatic cancer.
引用
收藏
页数:17
相关论文
共 128 条
[1]  
[Anonymous], CIRCULATING EXTRACEL
[2]  
[Anonymous], iExosomes in Treating Participants With Metastatic Pancreas Cancer With KrasG12D Mutation - Full Text View - ClinicalTrials.gov
[3]   Enhancement of Gemcitabine sensitivity in pancreatic adenocarcinoma by novel exosome-mediated delivery of the Survivin-T34A mutant [J].
Aspe, Jonathan R. ;
Osterman, Carlos J. Diaz ;
Jutzy, Jessica M. S. ;
Deshields, Simone ;
Whang, Sonia ;
Wall, Nathan R. .
JOURNAL OF EXTRACELLULAR VESICLES, 2014, 3 (01) :1-9
[4]   Pancreatic ductal adenocarcinoma: Risk factors, screening, and early detection [J].
Becker, Andrew E. ;
Hernandez, Yasmin G. ;
Frucht, Harold ;
Lucas, Aimee L. .
WORLD JOURNAL OF GASTROENTEROLOGY, 2014, 20 (32) :11182-11198
[5]   A microenvironment-inspired synthetic three-dimensional model for pancreatic ductal adenocarcinoma organoids [J].
Below, Christopher R. ;
Kelly, Joanna ;
Brown, Alexander ;
Humphries, Jonathan D. ;
Hutton, Colin ;
Xu, Jingshu ;
Lee, Brian Y. ;
Cintas, Celia ;
Zhang, Xiaohong ;
Hernandez-Gordillo, Victor ;
Stockdale, Linda ;
Goldsworthy, Matthew A. ;
Geraghty, Joe ;
Foster, Lucy ;
O'Reilly, Derek A. ;
Schedding, Barbara ;
Askari, Janet ;
Burns, Jessica ;
Hodson, Nigel ;
Smith, Duncan L. ;
Lally, Catherine ;
Ashton, Garry ;
Knight, David ;
Mironov, Aleksandr ;
Banyard, Antonia ;
Eble, Johannes A. ;
Morton, Jennifer P. ;
Humphries, Martin J. ;
Griffith, Linda G. ;
Jorgensen, Claus .
NATURE MATERIALS, 2022, 21 (01) :110-+
[6]   Transfer of miRNA in Macrophage-Derived Exosomes Induces Drug Resistance in Pancreatic Adenocarcinoma [J].
Binenbaum, Yoav ;
Fridman, Eran ;
Yaari, Zvi ;
Milman, Neta ;
Schroeder, Avi ;
Ben David, Gil ;
Shlomi, Tomer ;
Gil, Ziv .
CANCER RESEARCH, 2018, 78 (18) :5287-5299
[7]   Gemcitabine-releasing mesenchymal stromal cells inhibit in vitro proliferation of human pancreatic carcinoma cells [J].
Bonomi, Arianna ;
Sordi, Valeria ;
Dugnani, Erica ;
Ceserani, Valentina ;
Dossena, Marta ;
Cocce, Valentina ;
Cavicchini, Loredana ;
Ciusanj, Emilto ;
Bondiolotti, Gianpietro ;
Piovani, Giovanna ;
Pascucci, Luisa ;
Sisto, Francesca ;
Alessandri, Giulio ;
Piemonti, Lorenzo ;
Parati, Eugenjo ;
Pessina, Augusto .
CYTOTHERAPY, 2015, 17 (12) :1687-1695
[8]   Diabetes, antidiabetic medications, and pancreatic cancer risk: an analysis from the International Pancreatic Cancer Case-Control Consortium [J].
Bosetti, C. ;
Rosato, V. ;
Li, D. ;
Silverman, D. ;
Petersen, G. M. ;
Bracci, P. M. ;
Neale, R. E. ;
Muscat, J. ;
Anderson, K. ;
Gallinger, S. ;
Olson, S. H. ;
Miller, A. B. ;
Bueno-de-Mesquita, H. Bas ;
Scelo, G. ;
Janout, V. ;
Holcatova, I. ;
Lagiou, P. ;
Serraino, D. ;
Lucenteforte, E. ;
Fabianova, E. ;
Ghadirian, P. ;
Baghurst, P. A. ;
Zatonski, W. ;
Foretova, L. ;
Fontham, E. ;
Bamlet, W. R. ;
Holly, E. A. ;
Negri, E. ;
Hassan, M. ;
Prizment, A. ;
Cotterchio, M. ;
Cleary, S. ;
Kurtz, R. C. ;
Maisonneuve, P. ;
Trichopoulos, D. ;
Polesel, J. ;
Duell, E. J. ;
Boffetta, P. ;
La Vecchia, C. .
ANNALS OF ONCOLOGY, 2014, 25 (10) :2065-2072
[9]   High Clinical Value of Liquid Biopsy to Detect Circulating Tumor Cells and Tumor Exosomes in Pancreatic Ductal Adenocarcinoma Patients Eligible for Up-Front Surgery [J].
Buscail, Etienne ;
Alix-Panabieres, Catherine ;
Quincy, Pascaline ;
Cauvin, Thomas ;
Chauvet, Alexandre ;
Degrandi, Olivier ;
Caumont, Charline ;
Verdon, Severine ;
Lamrissi, Isabelle ;
Moranvillier, Isabelle ;
Buscail, Camille ;
Marty, Marion ;
Laurent, Christophe ;
Vendrely, Veronique ;
Moreau-Gaudry, Francois ;
Bedel, Aurelie ;
Dabernat, Sandrine ;
Chiche, Laurence .
CANCERS, 2019, 11 (11)
[10]   CD63-GPC1-Positive Exosomes Coupled with CA19-9 Offer Good Diagnostic Potential for Resectable Pancreatic Ductal Adenocarcinoma [J].
Buscail, Etienne ;
Chauvet, Alexandre ;
Quincy, Pascaline ;
Degrandi, Olivier ;
Buscail, Camille ;
Lamrissi, Isabelle ;
Moranvillier, Isabelle ;
Caumont, Charline ;
Verdon, Severine ;
Brisson, Alain ;
Marty, Marion ;
Chiche, Laurence ;
Laurent, Christophe ;
Vendrely, Veronique ;
Moreau-Gaudry, Francois ;
Bedel, Aurelie ;
Dabernat, Sandrine .
TRANSLATIONAL ONCOLOGY, 2019, 12 (11) :1395-1403