The potential role of tumor-derived exosomes in diagnosis, prognosis, and response to therapy in cancer

被引:41
作者
Czystowska-Kuzmicz, Malgorzata [1 ]
Whiteside, Theresa L. [2 ,3 ,4 ,5 ]
机构
[1] Med Univ Warsaw, Dept Biochem, Warsaw, Poland
[2] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA USA
[3] Univ Pittsburgh, Sch Med, Dept Immunol, Pittsburgh, PA USA
[4] Univ Pittsburgh, Sch Med, Dept Otolaryngol, Pittsburgh, PA USA
[5] UPMC Hillman Canc Ctr, Pittsburgh, PA 15213 USA
关键词
Cancer biomarkers; prognosis; response to therapy; small extracellular vesicles (sEV); tumor-derived exosomes (TEX); EXTRACELLULAR VESICLES; NECK-CANCER; HEPATOCELLULAR-CARCINOMA; COLORECTAL-CANCER; SUPPRESSOR-CELLS; INDUCE APOPTOSIS; T-CELLS; PLASMA; HEAD; MICROVESICLES;
D O I
10.1080/14712598.2020.1813276
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction Small extracellular vesicles (sEV) produced by tumors and called TEX mediate communication and regulate the tumor microenvironment. As a 'liquid tumor biopsy' and with the ability to induce pro-tumor reprogramming, TEX offer a promising approach to monitoring cancer progression or response to therapy. Areas covered TEX isolation from body fluids and separation by immunoaffinity capture from other EVs enables TEX molecular and functional characterization in vitro and in vivo. TEX carry membrane-bound PD-L1 and a rich cargo of other proteins and nucleic acids that reflect the tumor content and activity. TEX transfer this cargo to recipient cells, activating various molecular pathways and inducing pro-tumor transcriptional changes. TEX may interfere with immune therapies, and TEX plasma levels correlate with patients' responses to therapy. TEX induce local and systemic alterations in immune cells which may have a prognostic value. Expert opinion TEX have a special advantage as potential cancer biomarkers. Their cargo emerges as a correlate of developing or progressing malignant disease; their phenotype mimics that of the tumor; and their functional reprogramming of immune cells provides a reading of the patients' immune status prior and post immunotherapy. Validation of TEX and T-cell-derived sEV as cancer biomarkers is an impending future task.
引用
收藏
页码:241 / 258
页数:18
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