MicroRNA characteristics in epithelial ovarian cancer

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Standard

MicroRNA characteristics in epithelial ovarian cancer. / Prahm, Kira Philipsen; Høgdall, Claus Kim; Karlsen, Mona Aarenstrup; Christensen, Ib Jarle; Novotny, Guy Wayne; Høgdall, Estrid.

I: Plos One, Bind 16, Nr. 6, e0252401, 2021, s. 1-18.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Prahm, KP, Høgdall, CK, Karlsen, MA, Christensen, IJ, Novotny, GW & Høgdall, E 2021, 'MicroRNA characteristics in epithelial ovarian cancer', Plos One, bind 16, nr. 6, e0252401, s. 1-18. https://doi.org/10.1371/journal.pone.0252401

APA

Prahm, K. P., Høgdall, C. K., Karlsen, M. A., Christensen, I. J., Novotny, G. W., & Høgdall, E. (2021). MicroRNA characteristics in epithelial ovarian cancer. Plos One, 16(6), 1-18. [e0252401]. https://doi.org/10.1371/journal.pone.0252401

Vancouver

Prahm KP, Høgdall CK, Karlsen MA, Christensen IJ, Novotny GW, Høgdall E. MicroRNA characteristics in epithelial ovarian cancer. Plos One. 2021;16(6):1-18. e0252401. https://doi.org/10.1371/journal.pone.0252401

Author

Prahm, Kira Philipsen ; Høgdall, Claus Kim ; Karlsen, Mona Aarenstrup ; Christensen, Ib Jarle ; Novotny, Guy Wayne ; Høgdall, Estrid. / MicroRNA characteristics in epithelial ovarian cancer. I: Plos One. 2021 ; Bind 16, Nr. 6. s. 1-18.

Bibtex

@article{a24b0615666e499e94e5f184d768c6a8,
title = "MicroRNA characteristics in epithelial ovarian cancer",
abstract = "The purpose of the current study was to clarify differences in microRNA expression according to clinicopathological characteristics, and to investigate if miRNA profiles could predict cytoreductive outcome in patients with FIGO stage IIIC and IV ovarian cancer. Patients enrolled in the Pelvic Mass study between 2004 and 2010, diagnosed and surgically treated for epithelial ovarian cancer, were used for investigation. MicroRNA was profiled from tumour tissue with global microRNA microarray analysis. Differences in miRNA expression profiles were analysed according to histologic subtype, FIGO stage, tumour grade, type I or II tumours and result of primary cytoreductive surgery. One microRNA, miR-130a, which was found to be associated with serous histology and advanced FIGO stage, was also validated using data from external cohorts. Another seven microRNAs (miR-34a, miR-455-3p, miR-595, miR-1301, miR-146-5p, 193a-5p, miR-939) were found to be significantly associated with the clinicopathological characteristics (p ≤ 0.001), in our data, but mere not similarly significant when tested against external cohorts. Further validation in comparable cohorts, with microRNA profiled using newest and similar methods are warranted. ",
author = "Prahm, {Kira Philipsen} and H{\o}gdall, {Claus Kim} and Karlsen, {Mona Aarenstrup} and Christensen, {Ib Jarle} and Novotny, {Guy Wayne} and Estrid H{\o}gdall",
note = "Publisher Copyright: {\textcopyright} 2021 Prahm et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.",
year = "2021",
doi = "10.1371/journal.pone.0252401",
language = "English",
volume = "16",
pages = "1--18",
journal = "PLoS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "6",

}

RIS

TY - JOUR

T1 - MicroRNA characteristics in epithelial ovarian cancer

AU - Prahm, Kira Philipsen

AU - Høgdall, Claus Kim

AU - Karlsen, Mona Aarenstrup

AU - Christensen, Ib Jarle

AU - Novotny, Guy Wayne

AU - Høgdall, Estrid

N1 - Publisher Copyright: © 2021 Prahm et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

PY - 2021

Y1 - 2021

N2 - The purpose of the current study was to clarify differences in microRNA expression according to clinicopathological characteristics, and to investigate if miRNA profiles could predict cytoreductive outcome in patients with FIGO stage IIIC and IV ovarian cancer. Patients enrolled in the Pelvic Mass study between 2004 and 2010, diagnosed and surgically treated for epithelial ovarian cancer, were used for investigation. MicroRNA was profiled from tumour tissue with global microRNA microarray analysis. Differences in miRNA expression profiles were analysed according to histologic subtype, FIGO stage, tumour grade, type I or II tumours and result of primary cytoreductive surgery. One microRNA, miR-130a, which was found to be associated with serous histology and advanced FIGO stage, was also validated using data from external cohorts. Another seven microRNAs (miR-34a, miR-455-3p, miR-595, miR-1301, miR-146-5p, 193a-5p, miR-939) were found to be significantly associated with the clinicopathological characteristics (p ≤ 0.001), in our data, but mere not similarly significant when tested against external cohorts. Further validation in comparable cohorts, with microRNA profiled using newest and similar methods are warranted.

AB - The purpose of the current study was to clarify differences in microRNA expression according to clinicopathological characteristics, and to investigate if miRNA profiles could predict cytoreductive outcome in patients with FIGO stage IIIC and IV ovarian cancer. Patients enrolled in the Pelvic Mass study between 2004 and 2010, diagnosed and surgically treated for epithelial ovarian cancer, were used for investigation. MicroRNA was profiled from tumour tissue with global microRNA microarray analysis. Differences in miRNA expression profiles were analysed according to histologic subtype, FIGO stage, tumour grade, type I or II tumours and result of primary cytoreductive surgery. One microRNA, miR-130a, which was found to be associated with serous histology and advanced FIGO stage, was also validated using data from external cohorts. Another seven microRNAs (miR-34a, miR-455-3p, miR-595, miR-1301, miR-146-5p, 193a-5p, miR-939) were found to be significantly associated with the clinicopathological characteristics (p ≤ 0.001), in our data, but mere not similarly significant when tested against external cohorts. Further validation in comparable cohorts, with microRNA profiled using newest and similar methods are warranted.

UR - http://www.scopus.com/inward/record.url?scp=85107334819&partnerID=8YFLogxK

U2 - 10.1371/journal.pone.0252401

DO - 10.1371/journal.pone.0252401

M3 - Journal article

C2 - 34086724

AN - SCOPUS:85107334819

VL - 16

SP - 1

EP - 18

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 6

M1 - e0252401

ER -

ID: 304280656