Exosomal microRNAs in cancer: Potential biomarkers and immunotherapeutic targets for immune checkpoint molecules

被引:21
作者
Alotaibi, Faizah [1 ]
机构
[1] King Saud bin Abdulaziz Univ Hlth Sci, Coll Sci & Hlth Profess, King Abdullah Int Med Res Ctr, Minist Natl Guard Hlth Affairs, Riyadh, Saudi Arabia
关键词
exosomal miRNA; extracellular vesicles (EVs); cancer; small non-coding RNAs (sncRNAs); biomarker; clinical implication; liquid bioposy; immune checkpoint molecules; ACUTE MYELOID-LEUKEMIA; ACUTE LYMPHOBLASTIC-LEUKEMIA; CIRCULATING MICRORNAS; OVARIAN-CANCER; TEMOZOLOMIDE RESISTANCE; DIAGNOSTIC BIOMARKERS; CLINICAL-SIGNIFICANCE; TRANSFERRIN RECEPTOR; CELL-PROLIFERATION; TUMOR RECURRENCE;
D O I
10.3389/fgene.2023.1052731
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Exosomes are small extracellular vesicles with a lipid bilayer structure secreted from different cell types which can be found in various body fluids including blood, pleural fluid, saliva and urine. They carry different biomolecules including proteins, metabolites, and amino acids such as microRNAs which are small non-coding RNAs that regulate gene expression and promote cell-to-cell communication. One main function of the exosomal miRNAs (exomiRs) is their role in cancer pathogenesis. Alternation in exomiRs expression could indicate disease progression and can regulate cancer growth and facilitate drug response/resistance. It can also influence the tumour microenvironment by controlling important signaling that regulating immune checkpoint molecules leading to activation of T cell anti-tumour immunity. Therefore, they can be used as potential novel cancer biomarkers and innovative immunotherapeutic agents. This review highlights the use of exomiRs as potential reliable biomarkers for cancer diagnosis, treatment response and metastasis. Finally, discuses their potential as immunotherapeutic agents to regulate immune checkpoint molecules and promote T cell anti-tumour immunity.
引用
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页数:14
相关论文
共 149 条
[51]
Global microRNA expression profiling uncovers molecular markers for classification and prognosis in aggressive B-cell lymphoma [J].
Iqbal, Javeed ;
Shen, Yulei ;
Huang, Xin ;
Liu, Yanyan ;
Wake, Laura ;
Liu, Cuiling ;
Deffenbacher, Karen ;
Lachel, Cynthia M. ;
Wang, Chao ;
Rohr, Joseph ;
Guo, Shuangping ;
Smith, Lynette M. ;
Wright, George ;
Bhagavathi, Sharathkumar ;
Dybkaer, Karen ;
Fu, Kai ;
Greiner, Timothy C. ;
Vose, Julie M. ;
Jaffe, Elaine ;
Rimsza, Lisa ;
Rosenwald, Andreas ;
Ott, German ;
Delabie, Jan ;
Campo, Elias ;
Braziel, Rita M. ;
Cook, James R. ;
Tubbs, Raymond R. ;
Armitage, James O. ;
Weisenburger, Dennis D. ;
Staudt, Louis M. ;
Gascoyne, Randy D. ;
McKeithan, Timothy W. ;
Chan, Wing C. .
BLOOD, 2015, 125 (07) :1137-1145
[52]
Non-Coding RNAs of Extracellular Vesicles: Key Players in Organ-Specific Metastasis and Clinical Implications [J].
Jiang, Qian ;
Tan, Xiao-Ping ;
Zhang, Cai-Hua ;
Li, Zhi-Yuan ;
Li, Du ;
Xu, Yan ;
Liu, Yu Xuan ;
Wang, Lingzhi ;
Ma, Zhaowu .
CANCERS, 2022, 14 (22)
[53]
MicroRNA-221 sensitizes chronic myeloid leukemia cells to imatinib by targeting STAT5 [J].
Jiang, Xiaoxiao ;
Cheng, Yanhong ;
Hu, Chaojie ;
Zhang, Aimei ;
Ren, Yingli ;
Xu, Xiucai .
LEUKEMIA & LYMPHOMA, 2019, 60 (07) :1709-1720
[54]
Circulating exosomal MicroRNAs: New non-invasive biomarkers of non-communicable disease [J].
Jimenez-Avalos, Jorge Armando ;
Fernandez-Macias, Juan Carlos ;
Gonzalez-Palomo, Ana Karen .
MOLECULAR BIOLOGY REPORTS, 2021, 48 (01) :961-967
[55]
Prognostic value of miR-16 expression in childhood acute lymphoblastic leukemia relationships to normal and malignant lymphocyte proliferation [J].
Kaddar, T. ;
Chien, W. W. ;
Bertrand, Y. ;
Pages, M. P. ;
Rouault, J. P. ;
Salles, G. ;
Ffrench, M. ;
Magaud, J. P. .
LEUKEMIA RESEARCH, 2009, 33 (09) :1217-1223
[56]
Circulating miRNAs can serve as potential diagnostic biomarkers in chronic myelogenous leukemia patients [J].
Keramati, Farid ;
Jafarian, Arefeh ;
Soltani, Adele ;
Javandoost, Ehsan ;
Mollaei, Mojtaba ;
Fallah, Parviz .
LEUKEMIA RESEARCH REPORTS, 2021, 16
[57]
Human prostate cancer bone metastases have an actionable immunosuppressive microenvironment [J].
Kfoury, Youmna ;
Baryawno, Ninib ;
Severe, Nicolas ;
Mei, Shenglin ;
Gustafsson, Karin ;
Hirz, Taghreed ;
Brouse, Thomas ;
Scadden, Elizabeth W. ;
Igolkina, Anna A. ;
Kokkaliaris, Konstantinos ;
Choi, Bryan D. ;
Barkas, Nikolas ;
Randolph, Mark A. ;
Shin, John H. ;
Saylor, Philip J. ;
Scadden, David T. ;
Sykes, David B. ;
Kharchenko, Peter, V .
CANCER CELL, 2021, 39 (11) :1464-+
[58]
Expression differences of miR-142-5p between treatment-naive chronic myeloid leukemia patients responding and non-responding to imatinib therapy suggest a link to oncogenic ABL2, SRI, cKIT and MCL1 signaling pathways critical for development of therapy resistance [J].
Kluemper, Theresa ;
Bruckmueller, Henrike ;
Diewock, Tobias ;
Kaehler, Meike ;
Haenisch, Sierk ;
Pott, Christiane ;
Bruhn, Oliver ;
Cascorbi, Ingolf .
EXPERIMENTAL HEMATOLOGY & ONCOLOGY, 2020, 9 (01)
[59]
miRBase: annotating high confidence microRNAs using deep sequencing data [J].
Kozomara, Ana ;
Griffiths-Jones, Sam .
NUCLEIC ACIDS RESEARCH, 2014, 42 (D1) :D68-D73
[60]
New Concepts in Cancer Biomarkers: Circulating miRNAs in Liquid Biopsies [J].
Larrea, Erika ;
Sole, Carla ;
Manterola, Lorea ;
Goicoechea, Ibai ;
Armesto, Maria ;
Arestin, Maria ;
Caffarel, Maria M. ;
Araujo, Angela M. ;
Araiz, Maria ;
Fernandez-Mercado, Marta ;
Lawrie, Charles H. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (05)