Exosomes as a liquid biopsy for lung cancer

被引:140
作者
Cui, Shaohua [1 ,2 ]
Cheng, Zhuoan [3 ]
Qin, Wenxin [2 ]
Jiang, Liyan [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Resp Med, 241 HuaiHai W Rd, Shanghai 200030, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Renji Hosp, Shanghai Canc Inst,State Key Lab Oncogenes & Rela, 25 Ln 2200 Xie Tu Rd, Shanghai 200032, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Biomed Engn, Shanghai, Peoples R China
关键词
Lung cancer; Exosome; Liquid biopsy; Biomarker; ADENOCARCINOMA CELLS; CIRCULATING EXOSOMES; BIOGENESIS; SECRETION; BIOMARKER; PROTEINS; PLASMA; MICRORNA; HETEROGENEITY; MICROVESICLES;
D O I
10.1016/j.lungcan.2017.12.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In lung cancer and other malignancies, the so-called "liquid biopsy" is quickly moving into clinical practice. Its full potential has not yet been fully identified, but the "liquid biopsy" is no longer a promise but has become a reality that allows for better treatment selection and monitoring of lung cancer. This emerging field has significant potential to make up for the limitations of the traditional tissue-derived biomaterials. Exosomes are spherical nano-sized vesicles with a diameter of 40-100 nm and a density of 1.13-1.19 g/ml. In both physiological and pathological conditions, exosomes can be released by different cell types, including immune cells, stem cells and tumor cells. These small molecules may serve as promising biomarkers in lung cancer "liquid biopsy" as they can be easily obtained from most body fluids. In addition, the lipid bilayer of exosomes allows for stable cargoes which are relatively hard to degrade. Furthermore, the composition of exosomes reflects that of their parental cells, suggesting that exosomes are potential surrogates of the original cells and, therefore, are useful for understanding cell biology. Previous studies have demonstrated that exosomes play important roles in cell-to-cell communication. Moreover, tumor-derived exosomes are evolved in tumor-specific biological process, including tumor proliferation and progression. Recently, a growing number of studies has focused on exosomal cargo and their use in lung cancer genesis and progression. In addition, their utility as lung cancer diagnostic, prognostic and predictive biomarkers have also been studied. The current review primarily summaries lung cancer-related exosomal biomarkers that have recently been identified and discusses their potential in clinical practice.
引用
收藏
页码:46 / 54
页数:9
相关论文
共 77 条
[1]   Exosomal formulation enhances therapeutic response of celastrol against lung cancer [J].
Aqil, Farrukh ;
Kausar, Hina ;
Agrawal, Ashish Kumar ;
Jeyabalan, Jeyaprakash ;
Kyakulaga, Al-Hassan ;
Munagala, Radha ;
Gupta, Ramesh .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 2016, 101 (01) :12-21
[2]   Exosomes in cancer development, metastasis, and drug resistance: a comprehensive review [J].
Azmi, Asfar S. ;
Bao, Bin ;
Sarkar, Fazlul H. .
CANCER AND METASTASIS REVIEWS, 2013, 32 (3-4) :623-642
[3]   microRNAs Derived from Circulating Exosomes as Noninvasive Biomarkers for Screening and Diagnosing Lung Cancer [J].
Cazzoli, Riccardo ;
Buttitta, Fiamma ;
Di Nicola, Marta ;
Malatesta, Sara ;
Marchetti, Antonio ;
Rom, William N. ;
Pass, Harvey I. .
JOURNAL OF THORACIC ONCOLOGY, 2013, 8 (09) :1156-1162
[4]   Triple SILAC quantitative proteomic analysis reveals differential abundance of cell signaling proteins between normal and lung cancer-derived exosomes [J].
Clark, David J. ;
Fondrie, William E. ;
Yang, Austin ;
Mao, Li .
JOURNAL OF PROTEOMICS, 2016, 133 :161-169
[5]   Biogenesis, Secretion, and Intercellular Interactions of Exosomes and Other Extracellular Vesicles [J].
Colombo, Marina ;
Raposo, Graca ;
Thery, Clotilde .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 30, 2014, 30 :255-289
[6]   Analysis of ESCRT functions in exosome biogenesis, composition and secretion highlights the heterogeneity of extracellular vesicles [J].
Colombo, Marina ;
Moita, Catarina ;
van Niel, Guillaume ;
Kowal, Joanna ;
Vigneron, James ;
Benaroch, Philippe ;
Manel, Nicolas ;
Moita, Luis F. ;
Thery, Clotilde ;
Raposo, Graca .
JOURNAL OF CELL SCIENCE, 2013, 126 (24) :5553-5565
[7]   Tissue inhibitor of metalloproteinases-1 induces a pro-tumourigenic increase of miR-210 in lung adenocarcinoma cells and their exosomes [J].
Cui, H. ;
Seubert, B. ;
Stahl, E. ;
Dietz, H. ;
Reuning, U. ;
Moreno-Leon, L. ;
Ilie, M. ;
Hofman, P. ;
Nagase, H. ;
Mari, B. ;
Krueger, A. .
ONCOGENE, 2015, 34 (28) :3640-3650
[8]   Exosomal microRNA in plasma as a non-invasive biomarker for the recurrence of non-small cell lung cancer [J].
Dejima, Hitoshi ;
Iinuma, Hisae ;
Kanaoka, Rie ;
Matsutani, Noriyuki ;
Kawamura, Masafumi .
ONCOLOGY LETTERS, 2017, 13 (03) :1256-1263
[9]   Circulating miR-29a and miR-150 correlate with delivered dose during thoracic radiation therapy for non-small cell lung cancer [J].
Dinh, Tru-Khang T. ;
Fendler, Wojciech ;
Chalubinska-Fendler, Justyna ;
Acharya, Sanket S. ;
O'Leary, Colin ;
Deraska, Peter V. ;
D'Andrea, Alan D. ;
Chowdhury, Dipanjan ;
Kozono, David .
RADIATION ONCOLOGY, 2016, 11
[10]   Selective transfer of exosomes from oligodendrocytes to microglia by macropinocytosis [J].
Fitzner, Dirk ;
Schnaars, Mareike ;
van Rossum, Denise ;
Krishnamoorthy, Gurumoorthy ;
Dibaj, Payam ;
Bakhti, Mostafa ;
Regen, Tommy ;
Hanisch, Uwe-Karsten ;
Simons, Mikael .
JOURNAL OF CELL SCIENCE, 2011, 124 (03) :447-458