Review Article | | Peer-Reviewed

The Role of Exosomal Long Non-Coding RNAs in Tumors and Tumour Metabolism

Received: 10 July 2024     Accepted: 12 August 2024     Published: 27 August 2024
Views:       Downloads:
Abstract

Long non-coding RNAs (lncRNAs) are RNAs that do not have protein-coding functions and are involved in a wide range of important regulatory processes through four modes of (1) signaling (2) guidance (3) structural backbone (4) decoying, which regulate gene expression at epigenetic, transcriptional and post-transcriptional levels. Exosomes are extracellular vesicles released by various cells, whose contents are protected from degradation and stabilized in the extracellular environment due to their lipid bilayer membrane structure, and which are thought to play an important role in many diseases, including tumors. The exosomes secreted by tumor cells and stromal cells contain proteins, nucleic acids, lipids, cytokines, transcription factors and other biologically active substances. With the help of exosomes, they are stably transported between cells and mediate the exchange of substances and information between cells in order to achieve intercellular communication, thus affecting the biological activities of target cells. Among them, lncRNAs are selectively sorted into exosomes, which can regulate tumor metabolism as well as tumor progression through exosomes in various ways. In this paper, the role of exosomal lncRNAs in the tumor microenvironment and tumor metabolism is reviewed, with a view to providing markers, targets and directions for clinical diagnosis, tumor therapy and tumor-related research.

Published in American Journal of Biomedical and Life Sciences (Volume 12, Issue 3)
DOI 10.11648/j.ajbls.20241203.13
Page(s) 49-56
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Exosomes, Long Non-Coding RNA, Tumor Microenvironment, Tumor Metabolism

References
[1] Park E G, Pyo S J, Cui Y et al. Tumor Immune Microenvironment Lncrnas. Brief Bioinform, 2022, 1.
[2] Matsui M, Corey D R. Non-Coding Rnas as Drug Targets. Nat Rev Drug Discov, 2017, 3: 167-179.
[3] Struhl K. Transcriptional Noise and the Fidelity of Initiation by Rna Polymerase II. Nat Struct Mol Biol, 2007, 2: 103-105.
[4] Jarroux J, Morillon A, Pinskaya M. History, Discovery, and Classification of Lncrnas. Adv Exp Med Biol, 2017, 1-46.
[5] Bridges M C, Daulagala A C, Kourtidis A. Lnccation: Lncrna Localization and Function. J Cell Biol, 2021, 2.
[6] Zhu S, Wang Z, Xu J. Connecting Versatile Lncrnas with Heterogeneous Nuclear Ribonucleoprotein K and Pathogenic Disorders. Trends Biochem Sci, 2019, 9: 733-736.
[7] Moran V A, Niland C N, Khalil A M. Co-Immunoprecipitation of Long Noncoding Rnas. Methods Mol Biol, 2012, 219-228.
[8] Ashrafizadeh M, Rabiee N, Kumar A P et al. Long Noncoding Rnas (Lncrnas) in Pancreatic Cancer Progression. Drug Discov Today, 2022, 8: 2181-2198.
[9] Cao H L, Liu Z J, Huang P L et al. Lncrna-Rmrp Promotes Proliferation, Migration and Invasion of Bladder Cancer Via Mir-206. Eur Rev Med Pharmaco, 2019, 3: 1012-1021.
[10] Tao H, Zhang Y, Yuan T et al. Identification of an Emt-Related Lncrna Signature and Linc01116 as an Immune-Related Oncogene in Hepatocellular Carcinoma. Aging (Albany NY), 2022, 3: 1473-1491.
[11] He J, Zhu S, Liang X et al. Lncrna as a Multifunctional Regulator in Cancer Multi-Drug Resistance. Mol Biol Rep, 2021, 8: 1-15.
[12] Zhang Q, Li T, Wang Z et al. Lncrna Nr2F1-as1 Promotes Breast Cancer Angiogenesis through Activating Igf-1/Igf-1R/Erk Pathway. J Cell Mol Med, 2020, 14: 8236-8247.
[13] Xu Z, Peng B, Liang Q et al. Construction of a Ferroptosis-Related Nine-Lncrna Signature for Predicting Prognosis and Immune Response in Hepatocellular Carcinoma. Front Immunol, 2021, 719175.
[14] Xing C, Sun S G, Yue Z Q et al. Role of Lncrna Lucat1 in Cancer. Biomed Pharmacother, 2021, 111158.
[15] Grote P, Boon R A. Lncrnas Coming of Age. Circ Res, 2018, 5: 535-537.
[16] Kalra H, Drummen G P, Mathivanan S. Focus On Extracellular Vesicles: Introducing the Next Small Big Thing. Int J Mol Sci, 2016, 2: 170.
[17] Chen C, Luo Y, He W et al. Exosomal Long Noncoding Rna Lnmat2 Promotes Lymphatic Metastasis in Bladder Cancer. J Clin Invest, 2020, 1: 404-421.
[18] Linghan Tian, Xin Liu, Xicai Wang. Effect of exosome-derived lncRNA in tumor and its microenvironment. Chinese Journal of Tumor Biotherapy, 2019, 02: 236-240.
[19] Ahadi A, Brennan S, Kennedy P J et al. Long Non-Coding Rnas Harboring Mirna Seed Regions are Enriched in Prostate Cancer Exosomes. Sci Rep-Uk, 2016, 24922.
[20] Yiyong Wang, Yuyu Guan, Jingyun Du et al. Research progress of biomolecular markers in early diagnosis of ovarian cancer. Hebei Pharmaceutical, 2019, 18: 2855-2860. h
[21] Sundararajan V, Sarkar F H, Ramasamy T S. The Multifaceted Role of Exosomes in Cancer Progression: Diagnostic and Therapeutic Implications [Corrected]. Cell Oncol, 2018, 3: 223-252.
[22] Jia Y, Chen Y, Wang Q et al. Exosome: Emerging Biomarker in Breast Cancer. Oncotarget, 2017, 25: 41717-41733.
[23] Jing Guo, Linlin Xu, Xiaolong Wang et al. Exosome-derived Long Non-coding RNA H19 Promotes Cell Proliferation and Metastasis in Hepatocellular Carcinoma. Chinese Journal of Biochemistry and Molecular Biology, 2018, 12: 1325-1333.
[24] Ding L, Ren J, Zhang D et al. A Novel Stromal Lncrna Signature Reprograms Fibroblasts to Promote the Growth of Oral Squamous Cell Carcinoma Via Lncrna-Caf/Interleukin-33. Carcinogenesis, 2018, 3: 397-406.
[25] Han S, Qi Y, Luo Y et al. Exosomal Long Non-Coding Rna: Interaction Between Cancer Cells and Non-Cancer Cells. Front Oncol, 2020, 617837.
[26] Wang F, Ying H Q, He B S et al. Upregulated Lncrna-Uca1 Contributes to Progression of Hepatocellular Carcinoma through Inhibition of Mir-216B and Activation of Fgfr1/Erk Signaling Pathway. Oncotarget, 2015, 10: 7899-7917.
[27] Todorova D, Simoncini S, Lacroix R et al. Extracellular Vesicles in Angiogenesis. Circ Res, 2017, 10: 1658-1673.
[28] Nakamura K, Martin K C, Jackson J K et al. Brain-Derived Neurotrophic Factor Activation of Trkb Induces Vascular Endothelial Growth Factor Expression Via Hypoxia-Inducible Factor-1Alpha in Neuroblastoma Cells. Cancer Res, 2006, 8: 4249-4255.
[29] Qiu J J, Lin X J, Tang X Y et al. Exosomal Metastasis Associated Lung Adenocarcinoma Transcript 1 Promotes Angiogenesis and Predicts Poor Prognosis in Epithelial Ovarian Cancer. Int J Biol Sci, 2018, 14: 1960-1973.
[30] Chen Y, Zhou Y, Chen J et al. Exosomal Lncrna Snhg12 Promotes Angiogenesis and Breast Cancer Progression. Breast Cancer-Tokyo, 2024, 4: 607-620.
[31] Najafi M, Farhood B, Mortezaee K. Cancer Stem Cells (Cscs) in Cancer Progression and Therapy. J Cell Physiol, 2019, 6: 8381-8395.
[32] Tirino V, Desiderio V, Paino F et al. Cancer Stem Cells in Solid Tumors: An Overview and New Approaches for their Isolation and Characterization. Faseb J, 2013, 1: 13-24.
[33] Ren J, Ding L, Zhang D et al. Carcinoma-Associated Fibroblasts Promote the Stemness and Chemoresistance of Colorectal Cancer by Transferring Exosomal Lncrna H19. Theranostics, 2018, 14: 3932-3948.
[34] Li Z, Jiang P, Li J et al. Tumor-Derived Exosomal Lnc-Sox2Ot Promotes Emt and Stemness by Acting as a Cerna in Pancreatic Ductal Adenocarcinoma. Oncogene, 2018, 28: 3822-3838.
[35] Pastushenko I, Blanpain C. Emt Transition States During Tumor Progression and Metastasis. Trends Cell Biol, 2019, 3: 212-226.
[36] Chen C W, Fu M, Du ZH et al. Long Noncoding Rna Mrpl23-as1 Promotes Adenoid Cystic Carcinoma Lung Metastasis. Cancer Res, 2020, 11: 2273-2285.
[37] Pan L, Liang W, Fu M et al. Exosomes-Mediated Transfer of Long Noncoding Rna Zfas1 Promotes Gastric Cancer Progression. J Cancer Res Clin, 2017, 6: 991-1004.
[38] Piao H Y, Guo S, Wang Y et al. Exosome-Transmitted Lncrna Pcgem1 Promotes Invasive and Metastasis in Gastric Cancer by Maintaining the Stability of Snai1. Clin Transl Oncol, 2021, 2: 246-256.
[39] Qu L, Ding J, Chen C et al. Exosome-Transmitted Lncarsr Promotes Sunitinib Resistance in Renal Cancer by Acting as a Competing Endogenous Rna. Cancer Cell, 2016, 5: 653-668.
[40] Dong H, Wang W, Chen R et al. [Retracted] Exosome-Mediated Transfer of Lncrna Snhg14 Promotes Trastuzumab Chemoresistance in Breast Cancer. Int J Oncol, 2022, 2.
[41] Du Y, Kong G, You X et al. Elevation of Highly Up-Regulated in Liver Cancer (Hulc) by Hepatitis B Virus X Protein Promotes Hepatoma Cell Proliferation Via Down-Regulating P18. J Biol Chem, 2012, 31: 26302-26311.
[42] Li X, Lei Y, Wu M et al. Regulation of Macrophage Activation and Polarization by Hcc-Derived Exosomal Lncrna Tuc339. Int J Mol Sci, 2018, 10.
[43] Jiang R, Tang J, Chen Y et al. The Long Noncoding Rna Lnc-Egfr Stimulates T-Regulatory Cells Differentiation thus Promoting Hepatocellular Carcinoma Immune Evasion. Nat Commun, 2017, 15129.
[44] Chen J, Wang S, Jia S et al. Integrated Analysis of Long Non-Coding Rna and Mrna Expression Profile in Pancreatic Cancer Derived Exosomes Treated Dendritic Cells by Microarray Analysis. J Cancer, 2018, 1: 21-31.
[45] Long J, Zhang C J, Zhu N et al. Lipid Metabolism and Carcinogenesis, Cancer Development. Am J Cancer Res, 2018, 5: 778-791.
[46] Zou Z W, Ma C, Medoro L et al. Lncrna Anril is Up-Regulated in Nasopharyngeal Carcinoma and Promotes the Cancer Progression Via Increasing Proliferation, Reprograming Cell Glucose Metabolism and Inducing Side-Population Stem-Like Cancer Cells. Oncotarget, 2016, 38: 61741-61754.
[47] Zeng B, Ye H, Chen J et al. Lncrna Tug1 Sponges Mir-145 to Promote Cancer Progression and Regulate Glutamine Metabolism Via Sirt3/Gdh Axis. Oncotarget, 2017, 69: 113650-113661.
[48] Liu T, Han C, Fang P et al. Cancer-Associated Fibroblast-Specific Lncrna Linc01614 Enhances Glutamine Uptake in Lung Adenocarcinoma. J Hematol Oncol, 2022, 1: 141.
[49] Cui M, Xiao Z, Wang Y et al. Long Noncoding Rna Hulc Modulates Abnormal Lipid Metabolism in Hepatoma Cells through an Mir-9-Mediated Rxra Signaling Pathway. Cancer Res, 2015, 5: 846-857.
[50] Yingshi Lin, Hualin Tao. Diagnostic value of plasma exosomal lncRNA MALAT1 for breast cancer. Journal of Southwest Medical University, 2018, 02: 117-120.
Cite This Article
  • APA Style

    Luo, Y., Liu, Y., Jiang, Z. (2024). The Role of Exosomal Long Non-Coding RNAs in Tumors and Tumour Metabolism. American Journal of Biomedical and Life Sciences, 12(3), 49-56. https://doi.org/10.11648/j.ajbls.20241203.13

    Copy | Download

    ACS Style

    Luo, Y.; Liu, Y.; Jiang, Z. The Role of Exosomal Long Non-Coding RNAs in Tumors and Tumour Metabolism. Am. J. Biomed. Life Sci. 2024, 12(3), 49-56. doi: 10.11648/j.ajbls.20241203.13

    Copy | Download

    AMA Style

    Luo Y, Liu Y, Jiang Z. The Role of Exosomal Long Non-Coding RNAs in Tumors and Tumour Metabolism. Am J Biomed Life Sci. 2024;12(3):49-56. doi: 10.11648/j.ajbls.20241203.13

    Copy | Download

  • @article{10.11648/j.ajbls.20241203.13,
      author = {Yaomin Luo and Yanhong Liu and Zhen Jiang},
      title = {The Role of Exosomal Long Non-Coding RNAs in Tumors and Tumour Metabolism
    },
      journal = {American Journal of Biomedical and Life Sciences},
      volume = {12},
      number = {3},
      pages = {49-56},
      doi = {10.11648/j.ajbls.20241203.13},
      url = {https://doi.org/10.11648/j.ajbls.20241203.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajbls.20241203.13},
      abstract = {Long non-coding RNAs (lncRNAs) are RNAs that do not have protein-coding functions and are involved in a wide range of important regulatory processes through four modes of (1) signaling (2) guidance (3) structural backbone (4) decoying, which regulate gene expression at epigenetic, transcriptional and post-transcriptional levels. Exosomes are extracellular vesicles released by various cells, whose contents are protected from degradation and stabilized in the extracellular environment due to their lipid bilayer membrane structure, and which are thought to play an important role in many diseases, including tumors. The exosomes secreted by tumor cells and stromal cells contain proteins, nucleic acids, lipids, cytokines, transcription factors and other biologically active substances. With the help of exosomes, they are stably transported between cells and mediate the exchange of substances and information between cells in order to achieve intercellular communication, thus affecting the biological activities of target cells. Among them, lncRNAs are selectively sorted into exosomes, which can regulate tumor metabolism as well as tumor progression through exosomes in various ways. In this paper, the role of exosomal lncRNAs in the tumor microenvironment and tumor metabolism is reviewed, with a view to providing markers, targets and directions for clinical diagnosis, tumor therapy and tumor-related research.
    },
     year = {2024}
    }
    

    Copy | Download

  • TY  - JOUR
    T1  - The Role of Exosomal Long Non-Coding RNAs in Tumors and Tumour Metabolism
    
    AU  - Yaomin Luo
    AU  - Yanhong Liu
    AU  - Zhen Jiang
    Y1  - 2024/08/27
    PY  - 2024
    N1  - https://doi.org/10.11648/j.ajbls.20241203.13
    DO  - 10.11648/j.ajbls.20241203.13
    T2  - American Journal of Biomedical and Life Sciences
    JF  - American Journal of Biomedical and Life Sciences
    JO  - American Journal of Biomedical and Life Sciences
    SP  - 49
    EP  - 56
    PB  - Science Publishing Group
    SN  - 2330-880X
    UR  - https://doi.org/10.11648/j.ajbls.20241203.13
    AB  - Long non-coding RNAs (lncRNAs) are RNAs that do not have protein-coding functions and are involved in a wide range of important regulatory processes through four modes of (1) signaling (2) guidance (3) structural backbone (4) decoying, which regulate gene expression at epigenetic, transcriptional and post-transcriptional levels. Exosomes are extracellular vesicles released by various cells, whose contents are protected from degradation and stabilized in the extracellular environment due to their lipid bilayer membrane structure, and which are thought to play an important role in many diseases, including tumors. The exosomes secreted by tumor cells and stromal cells contain proteins, nucleic acids, lipids, cytokines, transcription factors and other biologically active substances. With the help of exosomes, they are stably transported between cells and mediate the exchange of substances and information between cells in order to achieve intercellular communication, thus affecting the biological activities of target cells. Among them, lncRNAs are selectively sorted into exosomes, which can regulate tumor metabolism as well as tumor progression through exosomes in various ways. In this paper, the role of exosomal lncRNAs in the tumor microenvironment and tumor metabolism is reviewed, with a view to providing markers, targets and directions for clinical diagnosis, tumor therapy and tumor-related research.
    
    VL  - 12
    IS  - 3
    ER  - 

    Copy | Download

Author Information
  • Sections