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Increased levels of microRNA‐320 in blood serum and plasma is associated with imminent and advanced lung cancer

Lung cancer (LC) incidence is increasing globally and altered levels of microRNAs (miRNAs) in blood may contribute to identification of individuals with LC. We identified miRNAs differentially expressed in peripheral blood at LC diagnosis and evaluated, in pre‐diagnostic blood specimens, how long be...

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Autores principales: Nøst, Therese Haugdahl, Skogholt, Anne Heidi, Urbarova, Ilona, Mjelle, Robin, Paulsen, Erna‐Elise, Dønnem, Tom, Andersen, Sigve, Markaki, Maria, Røe, Oluf Dimitri, Johansson, Mikael, Johansson, Mattias, Grønberg, Bjørn Henning, Sandanger, Torkjel Manning, Sætrom, Pål
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892825/
https://www.ncbi.nlm.nih.gov/pubmed/36337027
http://dx.doi.org/10.1002/1878-0261.13336
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author Nøst, Therese Haugdahl
Skogholt, Anne Heidi
Urbarova, Ilona
Mjelle, Robin
Paulsen, Erna‐Elise
Dønnem, Tom
Andersen, Sigve
Markaki, Maria
Røe, Oluf Dimitri
Johansson, Mikael
Johansson, Mattias
Grønberg, Bjørn Henning
Sandanger, Torkjel Manning
Sætrom, Pål
author_facet Nøst, Therese Haugdahl
Skogholt, Anne Heidi
Urbarova, Ilona
Mjelle, Robin
Paulsen, Erna‐Elise
Dønnem, Tom
Andersen, Sigve
Markaki, Maria
Røe, Oluf Dimitri
Johansson, Mikael
Johansson, Mattias
Grønberg, Bjørn Henning
Sandanger, Torkjel Manning
Sætrom, Pål
author_sort Nøst, Therese Haugdahl
collection PubMed
description Lung cancer (LC) incidence is increasing globally and altered levels of microRNAs (miRNAs) in blood may contribute to identification of individuals with LC. We identified miRNAs differentially expressed in peripheral blood at LC diagnosis and evaluated, in pre‐diagnostic blood specimens, how long before diagnosis expression changes in such candidate miRNAs could be detected. We identified upregulated candidate miRNAs in plasma specimens from a hospital‐based study sample of 128 patients with confirmed LC and 62 individuals with suspected but confirmed negative LC (FalsePos). We then evaluated the expression of candidate miRNAs in pre‐diagnostic plasma or serum specimens of 360 future LC cases and 375 matched controls. There were 1663 miRNAs detected in diagnostic specimens, nine of which met our criteria for candidate miRNAs. Higher expression of three candidates, miR‐320b, 320c, and 320d, was associated with poor survival, independent of LC stage and subtype. Moreover, miR‐320c and miR‐320d expression was higher in pre‐diagnostic specimens collected within 2 years of LC diagnosis. Our results indicated that elevated levels of miR‐320c and miR‐320d may be early indications of imminent and advanced LC.
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spelling pubmed-98928252023-02-06 Increased levels of microRNA‐320 in blood serum and plasma is associated with imminent and advanced lung cancer Nøst, Therese Haugdahl Skogholt, Anne Heidi Urbarova, Ilona Mjelle, Robin Paulsen, Erna‐Elise Dønnem, Tom Andersen, Sigve Markaki, Maria Røe, Oluf Dimitri Johansson, Mikael Johansson, Mattias Grønberg, Bjørn Henning Sandanger, Torkjel Manning Sætrom, Pål Mol Oncol Research Articles Lung cancer (LC) incidence is increasing globally and altered levels of microRNAs (miRNAs) in blood may contribute to identification of individuals with LC. We identified miRNAs differentially expressed in peripheral blood at LC diagnosis and evaluated, in pre‐diagnostic blood specimens, how long before diagnosis expression changes in such candidate miRNAs could be detected. We identified upregulated candidate miRNAs in plasma specimens from a hospital‐based study sample of 128 patients with confirmed LC and 62 individuals with suspected but confirmed negative LC (FalsePos). We then evaluated the expression of candidate miRNAs in pre‐diagnostic plasma or serum specimens of 360 future LC cases and 375 matched controls. There were 1663 miRNAs detected in diagnostic specimens, nine of which met our criteria for candidate miRNAs. Higher expression of three candidates, miR‐320b, 320c, and 320d, was associated with poor survival, independent of LC stage and subtype. Moreover, miR‐320c and miR‐320d expression was higher in pre‐diagnostic specimens collected within 2 years of LC diagnosis. Our results indicated that elevated levels of miR‐320c and miR‐320d may be early indications of imminent and advanced LC. John Wiley and Sons Inc. 2022-11-27 /pmc/articles/PMC9892825/ /pubmed/36337027 http://dx.doi.org/10.1002/1878-0261.13336 Text en © 2022 The Authors. Molecular Oncology published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Nøst, Therese Haugdahl
Skogholt, Anne Heidi
Urbarova, Ilona
Mjelle, Robin
Paulsen, Erna‐Elise
Dønnem, Tom
Andersen, Sigve
Markaki, Maria
Røe, Oluf Dimitri
Johansson, Mikael
Johansson, Mattias
Grønberg, Bjørn Henning
Sandanger, Torkjel Manning
Sætrom, Pål
Increased levels of microRNA‐320 in blood serum and plasma is associated with imminent and advanced lung cancer
title Increased levels of microRNA‐320 in blood serum and plasma is associated with imminent and advanced lung cancer
title_full Increased levels of microRNA‐320 in blood serum and plasma is associated with imminent and advanced lung cancer
title_fullStr Increased levels of microRNA‐320 in blood serum and plasma is associated with imminent and advanced lung cancer
title_full_unstemmed Increased levels of microRNA‐320 in blood serum and plasma is associated with imminent and advanced lung cancer
title_short Increased levels of microRNA‐320 in blood serum and plasma is associated with imminent and advanced lung cancer
title_sort increased levels of microrna‐320 in blood serum and plasma is associated with imminent and advanced lung cancer
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892825/
https://www.ncbi.nlm.nih.gov/pubmed/36337027
http://dx.doi.org/10.1002/1878-0261.13336
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