Exosomal Long Non-coding RNAs: Emerging Players in the Tumor Microenvironment

被引:50
作者
Pathania, Anup S. [1 ,2 ]
Challagundla, Kishore B. [1 ,2 ,3 ]
机构
[1] Univ Nebraska Med Ctr, Dept Biochem & Mol Biol, 985870 Nebraska Med Ctr, Omaha, NE 68198 USA
[2] Univ Nebraska Med Ctr, Fred & Pamela Buffet Canc Ctr, 985870 Nebraska Med Ctr, Omaha, NE 68198 USA
[3] Univ Nebraska Med Ctr, Childrens Hlth Res Inst, Omaha, NE 68198 USA
关键词
CELL-DERIVED EXOSOMES; EXTRACELLULAR VESICLES; COLORECTAL-CANCER; LNCRNA; PROMOTE; INVASION; PROGRESSION; EXPRESSION; MICRORNAS; AUTOPHAGY;
D O I
10.1016/j.omtn.2020.09.039
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Recent advances in exosome biology have uncovered a significant role of exosomes in cancer and make them a determining factor in intercellular communication. Exosomes are types of extracellular vesicles that are involved in the communication between cells by exchanging various signaling molecules between the surrounding cells. Among various signaling molecules, long non-coding RNAs (lncRNAs), a type of non-coding RNA having a size of more than 200 nt in length and lacking protein-coding potential, have emerged as crucial regulators of intercellular communication. Tumor-derived exosomes containing various lncRNAs, known as exosomal lncRNAs, reprogram the microenvironment by regulating numerous cellular functions, including the regulation of gene transcription that favors cancer growth and progression, thus significantly determining the biological effects of exosomes. In addition, deregulated expression of lncRNAs is found in various human cancers and serves as a diagnostic biomarker to predict cancer type. The present review discusses the role of exosomal lncRNAs in the crosstalk between tumor cells and the surrounding cells of the microenvironment. Furthermore, we also discuss the involvement of exosomal lncRNAs within the tumor microenvironment in favoring tumor growth, metabolic reprogramming of tumor cells, and tumor-supportive autophagy. Therefore, lncRNAs can be used as a therapeutic target in the treatment of various human cancers.
引用
收藏
页码:1371 / 1383
页数:13
相关论文
共 152 条
[1]   TUMOR-DERIVED URINARY EXOSOMAL LONG NON-CODING RNAs AS DIAGNOSTIC BIOMARKERS FOR BLADDER CANCER [J].
Abbastabar, Maryam ;
Sarfi, Mohammad ;
Golestani, Abolfazl ;
Karimi, Ali ;
Pourmand, Gholamreza ;
Khalili, Ehsan .
EXCLI JOURNAL, 2020, 19 :301-310
[2]   MicroRNAs and other tiny endogenous RNAs in C-elegans [J].
Ambros, V ;
Lee, RC ;
Lavanway, A ;
Williams, PT ;
Jewell, D .
CURRENT BIOLOGY, 2003, 13 (10) :807-818
[3]   Delivering the promise of RNA therapeutics [J].
不详 .
NATURE MEDICINE, 2019, 25 (09) :1321-1321
[4]   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
[5]  
Bae Susan, 2018, Genes Cancer, V9, P87, DOI 10.18632/genesandcancer.172
[6]   Exosomes: New players in cell-cell communication [J].
Bang, Claudia ;
Thum, Thomas .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2012, 44 (11) :2060-2064
[7]   The Intronic Long Noncoding RNA ANRASSF1 Recruits PRC2 to the RASSF1A Promoter, Reducing the Expression of RASSF1A and Increasing Cell Proliferation [J].
Beckedorff, Felipe C. ;
Ayupe, Ana C. ;
Crocci-Souza, Renan ;
Amaral, Murilo S. ;
Nakaya, Helder I. ;
Soltys, Daniela T. ;
Menck, Carlos F. M. ;
Reis, Eduardo M. ;
Verjovski-Almeida, Sergio .
PLOS GENETICS, 2013, 9 (08)
[8]   Exosome in Cardiovascular Diseases: A Complex World Full of Hope [J].
Bellin, Gloria ;
Gardin, Chiara ;
Ferroni, Letizia ;
Chachques, Juan Carlos ;
Rogante, Massimo ;
Mitrecic, Dinko ;
Ferrari, Roberto ;
Zavan, Barbara .
CELLS, 2019, 8 (02)
[9]   Activated T Cell Exosomes Promote Tumor Invasion via Fas Signaling Pathway [J].
Cai, Zhijian ;
Yang, Fei ;
Yu, Lei ;
Yu, Zhou ;
Jiang, Lingling ;
Wang, Qingqing ;
Yang, Yunshan ;
Wang, Lie ;
Cao, Xuetao ;
Wang, Jianli .
JOURNAL OF IMMUNOLOGY, 2012, 188 (12) :5954-5961
[10]   The transcriptional landscape of the mammalian genome [J].
Carninci, P ;
Kasukawa, T ;
Katayama, S ;
Gough, J ;
Frith, MC ;
Maeda, N ;
Oyama, R ;
Ravasi, T ;
Lenhard, B ;
Wells, C ;
Kodzius, R ;
Shimokawa, K ;
Bajic, VB ;
Brenner, SE ;
Batalov, S ;
Forrest, ARR ;
Zavolan, M ;
Davis, MJ ;
Wilming, LG ;
Aidinis, V ;
Allen, JE ;
Ambesi-Impiombato, X ;
Apweiler, R ;
Aturaliya, RN ;
Bailey, TL ;
Bansal, M ;
Baxter, L ;
Beisel, KW ;
Bersano, T ;
Bono, H ;
Chalk, AM ;
Chiu, KP ;
Choudhary, V ;
Christoffels, A ;
Clutterbuck, DR ;
Crowe, ML ;
Dalla, E ;
Dalrymple, BP ;
de Bono, B ;
Della Gatta, G ;
di Bernardo, D ;
Down, T ;
Engstrom, P ;
Fagiolini, M ;
Faulkner, G ;
Fletcher, CF ;
Fukushima, T ;
Furuno, M ;
Futaki, S ;
Gariboldi, M .
SCIENCE, 2005, 309 (5740) :1559-1563