Competitive Endogenous RNA Network Involving miRNA and lncRNA in Non-Hodgkin Lymphoma: Current Advances and Clinical Perspectives
Non-Hodgkin lymphoma (NHL) is a heterogeneous malignancy with variable patient outcomes. There is still a lack of understanding about the different players involved in lymphomagenesis, and the identification of new diagnostic and prognostic biomarkers is urgent. MicroRNAs and long non-coding RNAs em...
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Published in | Biomedicines Vol. 9; no. 12; p. 1934 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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17.12.2021
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Abstract | Non-Hodgkin lymphoma (NHL) is a heterogeneous malignancy with variable patient outcomes. There is still a lack of understanding about the different players involved in lymphomagenesis, and the identification of new diagnostic and prognostic biomarkers is urgent. MicroRNAs and long non-coding RNAs emerged as master regulators of B-cell development, and their deregulation has been associated with the initiation and progression of lymphomagenesis. They can function by acting alone or, as recently proposed, by creating competing endogenous RNA (ceRNA) networks. Most studies have focused on individual miRNAs/lncRNAs function in lymphoma, and there is still limited data regarding their interactions in lymphoma progression. The study of miRNAs' and lncRNAs' deregulation in NHL, either alone or as ceRNAs networks, offers new insights into the molecular mechanisms underlying lymphoma pathogenesis and opens a window of opportunity to identify potential diagnostic and prognostic biomarkers. In this review, we summarized the current knowledge regarding the role of miRNAs and lncRNAs in B-cell lymphoma, including their interactions and regulatory networks. Finally, we summarized the studies investigating the potential of miRNAs and lncRNAs as clinical biomarkers, with a special focus on the circulating profiles, to be applied as a non-invasive, easy-to-obtain, and reproducible liquid biopsy for dynamic management of NHL patients. |
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AbstractList | Non-Hodgkin lymphoma (NHL) is a heterogeneous malignancy with variable patient outcomes. There is still a lack of understanding about the different players involved in lymphomagenesis, and the identification of new diagnostic and prognostic biomarkers is urgent. MicroRNAs and long non-coding RNAs emerged as master regulators of B-cell development, and their deregulation has been associated with the initiation and progression of lymphomagenesis. They can function by acting alone or, as recently proposed, by creating competing endogenous RNA (ceRNA) networks. Most studies have focused on individual miRNAs/lncRNAs function in lymphoma, and there is still limited data regarding their interactions in lymphoma progression. The study of miRNAs’ and lncRNAs’ deregulation in NHL, either alone or as ceRNAs networks, offers new insights into the molecular mechanisms underlying lymphoma pathogenesis and opens a window of opportunity to identify potential diagnostic and prognostic biomarkers. In this review, we summarized the current knowledge regarding the role of miRNAs and lncRNAs in B-cell lymphoma, including their interactions and regulatory networks. Finally, we summarized the studies investigating the potential of miRNAs and lncRNAs as clinical biomarkers, with a special focus on the circulating profiles, to be applied as a non-invasive, easy-to-obtain, and reproducible liquid biopsy for dynamic management of NHL patients. |
Author | Fernandes, Mara Marques, Herlander Teixeira, Ana Luísa Medeiros, Rui |
AuthorAffiliation | 4 Life and Health Sciences Research Institute (ICVS), School of Medicine, Campus de Gualtar, University of Minho, 4710-057 Braga, Portugal; herlandermarques@hotmail.com 1 Molecular Oncology and Viral Pathology Group, Research Center of IPO Porto (CI-IPOP)/RISE@CI-IPOP (Health Research Network), Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center (Porto.CCC), 4200-072 Porto, Portugal; mara.aires.fernandes@ipoporto.min-saude.pt (M.F.); ana.luisa.teixeira@ipoporto.min-saude.pt (A.L.T.) 7 CINTESIS, Center for Health Technology and Services Research, Faculty of Medicine, University of Porto, 4200-450 Porto, Portugal 3 Faculty of Medicine, University of Porto (FMUP), 4200-319 Porto, Portugal 6 Department of Oncology, Hospital de Braga, 4710-243 Braga, Portugal 9 Biomedical Research Center (CEBIMED), Faculty of Health Sciences of Fernando Pessoa University (UFP), 4249-004 Porto, Portugal 2 Research Department of the Portuguese League against Cancer Regional Nucleus |
AuthorAffiliation_xml | – name: 6 Department of Oncology, Hospital de Braga, 4710-243 Braga, Portugal – name: 9 Biomedical Research Center (CEBIMED), Faculty of Health Sciences of Fernando Pessoa University (UFP), 4249-004 Porto, Portugal – name: 7 CINTESIS, Center for Health Technology and Services Research, Faculty of Medicine, University of Porto, 4200-450 Porto, Portugal – name: 3 Faculty of Medicine, University of Porto (FMUP), 4200-319 Porto, Portugal – name: 1 Molecular Oncology and Viral Pathology Group, Research Center of IPO Porto (CI-IPOP)/RISE@CI-IPOP (Health Research Network), Portuguese Oncology Institute of Porto (IPO Porto)/Porto Comprehensive Cancer Center (Porto.CCC), 4200-072 Porto, Portugal; mara.aires.fernandes@ipoporto.min-saude.pt (M.F.); ana.luisa.teixeira@ipoporto.min-saude.pt (A.L.T.) – name: 8 ICBAS—Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, 4050-513 Porto, Portugal – name: 4 Life and Health Sciences Research Institute (ICVS), School of Medicine, Campus de Gualtar, University of Minho, 4710-057 Braga, Portugal; herlandermarques@hotmail.com – name: 2 Research Department of the Portuguese League against Cancer Regional Nucleus of the North (LPCC-NRN), 4200-177 Porto, Portugal – name: 5 ICVS/3B’s–PT Government Associate Laboratory, 4805-017 Braga/Guimarães, Portugal |
Author_xml | – sequence: 1 givenname: Mara orcidid: 0000-0001-9023-1109 surname: Fernandes fullname: Fernandes, Mara email: RISE@CI-IPOP organization: Faculty of Medicine, University of Porto (FMUP), 4200-319 Porto, Portugal – sequence: 2 givenname: Herlander orcidid: 0000-0002-5854-4444 surname: Marques fullname: Marques, Herlander organization: CINTESIS, Center for Health Technology and Services Research, Faculty of Medicine, University of Porto, 4200-450 Porto, Portugal – sequence: 3 givenname: Ana Luísa orcidid: 0000-0002-7489-2211 surname: Teixeira fullname: Teixeira, Ana Luísa email: RISE@CI-IPOP organization: ICBAS-Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, 4050-513 Porto, Portugal – sequence: 4 givenname: Rui orcidid: 0000-0003-3010-8373 surname: Medeiros fullname: Medeiros, Rui email: RISE@CI-IPOP organization: Biomedical Research Center (CEBIMED), Faculty of Health Sciences of Fernando Pessoa University (UFP), 4249-004 Porto, Portugal |
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Snippet | Non-Hodgkin lymphoma (NHL) is a heterogeneous malignancy with variable patient outcomes. There is still a lack of understanding about the different players... |
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SubjectTerms | B-cell lymphoma Biomarkers Biopsy Cell cycle Cell growth Chemotherapy Gene expression lncRNAs Lymphocytes B Lymphoma Malignancy Medical prognosis MicroRNAs miRNA miRNAs Molecular modelling Non-coding RNA Non-Hodgkin's lymphoma Pathogenesis Patients Review Transcription factors |
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Title | Competitive Endogenous RNA Network Involving miRNA and lncRNA in Non-Hodgkin Lymphoma: Current Advances and Clinical Perspectives |
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