The involvement of exosomes in the diagnosis and treatment of pancreatic cancer

被引:86
作者
Ariston Gabriel, Abakundana Nsenga [1 ,2 ]
Wang, Fang [3 ]
Jiao, Qinlian [1 ,4 ]
Yvette, Umwali [2 ,5 ]
Yang, Xuemei [1 ]
Al-Ameri, Samed Ahmed [1 ,2 ]
Du, Lutao [1 ]
Wang, Yun-shan [1 ]
Wang, Chuanxin [1 ]
机构
[1] Shandong Univ, Second Hosp, Dept Clin Lab, Cheeloo Coll Med, Jinan 250033, Shandong, Peoples R China
[2] Shandong Univ, Sch Med, Dept Clin Lab Diagnost, Cheeloo Coll Med, Jinan 250012, Shandong, Peoples R China
[3] Shandong Univ, Inst Med Sci, Second Hosp, Cheeloo Coll Med, Jinan 250033, Shandong, Peoples R China
[4] Shandong Univ, Marine Coll, Weihai 264209, Peoples R China
[5] Shandong Univ, Qilu Hosp, Dept Clin Lab, Cheeloo Coll Med, Jinan 250012, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Exosomes; Pancreatic cancer; Biomarker; Treatment; METASTASIS; RISK;
D O I
10.1186/s12943-020-01245-y
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
At the moment, pancreatic cancer is among the deadliest gastrointestinal diseases, and pancreatic cancer growth is a complex biological process that is based on different kinds of genes. Exosomes are extracellular vesicles containing microRNAs (miRNAs), messenger RNA (mRNA), and proteins, they act as the most prominent mediator of intercellular communication, and they regulate, instruct, and re-educate their surrounding microenvironment and target specific organs. Due to accumulative evidence proved that exosomes are involved in metastasis, cell proliferation, EMT, angiogenesis, and TME of pancreatic cancer, exosomes are crucial potential candidates to detect pancreatic cancer early. This review aims to convey the current understanding of the main functions employed by exosomes in early diagnosis and treatment of pancreatic cancer.
引用
收藏
页数:9
相关论文
共 95 条
[21]  
Hannafon BN, 2013, INT J MOL SCI
[22]   Heterogeneity of KRAS Mutations in Pancreatic Ductal Adenocarcinoma [J].
Hashimoto, Daisuke ;
Arima, Kota ;
Yokoyama, Naomi ;
Chikamoto, Akira ;
Taki, Katsunobu ;
Inoue, Risa ;
Kaida, Takayoshi ;
Higashi, Takaaki ;
Nitta, Hidetoshi ;
Ohmuraya, Masaki ;
Hirota, Masahiko ;
Beppu, Toru ;
Baba, Hideo .
PANCREAS, 2016, 45 (08) :1111-1114
[23]   Trp53R172H and KraSG12D cooperate to promote chromosomal instability and widely metastatic pancreatic ductal adenocarcinoma in mice [J].
Hingorani, SR ;
Wang, LF ;
Multani, AS ;
Combs, C ;
Deramaudt, TB ;
Hruban, RH ;
Rustgi, AK ;
Chang, S ;
Tuveson, DA .
CANCER CELL, 2005, 7 (05) :469-483
[24]   MiR-361-3p regulates ERK1/2-induced EMT via DUSP2 mRNA degradation in pancreatic ductal adenocarcinoma [J].
Hu, Jisheng ;
Li, Le ;
Chen, Hongze ;
Zhang, Guangquan ;
Liu, Huan ;
Kong, Rui ;
Chen, Hua ;
Wang, Yongwei ;
Li, Yilong ;
Tian, Fengyu ;
Lv, Xinjian ;
Li, Guanqun ;
Sun, Bei .
CELL DEATH & DISEASE, 2018, 9
[25]   Focus on Extracellular Vesicles: Physiological Role and Signalling Properties of Extracellular Membrane Vesicles [J].
Iraci, Nunzio ;
Leonardi, Tommaso ;
Gessler, Florian ;
Vega, Beatriz ;
Pluchino, Stefano .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (02)
[26]  
Joshi GK, 2015, ACS NANO
[27]   MicroRNA-21 in Pancreatic Ductal Adenocarcinoma Tumor-Associated Fibroblasts Promotes Metastasis [J].
Kadera, Brian E. ;
Li, Luyi ;
Toste, Paul A. ;
Wu, Nanping ;
Adams, Curtis ;
Dawson, David W. ;
Donahue, Timothy R. .
PLOS ONE, 2013, 8 (08)
[28]  
Kahlert C, 2014, J Biol Chem
[29]   The biology and function of exosomes in cancer [J].
Kalluri, Raghu .
JOURNAL OF CLINICAL INVESTIGATION, 2016, 126 (04) :1208-1215
[30]  
Kamerkar S, 2017, NATURE