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Differential Expression of lincRNA-ROR Spliced Transcript Variants in Breast Cancer

BACKGROUND: We investigated the expression pattern of a human stem cell-specific, large intergenic noncoding RNA (lincRNA) regulator of reprogramming (lincRNA-ROR) and its spliced transcript variants in breast tumors. Breast cancer is the leading cause of cancer mortality in women; therefore, findin...

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Autores principales: Saadat Akhtar, Mozhgan, Gholipour, Akram, Bagheri Moghaddam, Mahrokh, Oveisee, Maziar, Mowla, Seyed Javad, Malakootian, Mahshid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113567/
https://www.ncbi.nlm.nih.gov/pubmed/37089151
http://dx.doi.org/10.18502/ijph.v52i2.11896
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author Saadat Akhtar, Mozhgan
Gholipour, Akram
Bagheri Moghaddam, Mahrokh
Oveisee, Maziar
Mowla, Seyed Javad
Malakootian, Mahshid
author_facet Saadat Akhtar, Mozhgan
Gholipour, Akram
Bagheri Moghaddam, Mahrokh
Oveisee, Maziar
Mowla, Seyed Javad
Malakootian, Mahshid
author_sort Saadat Akhtar, Mozhgan
collection PubMed
description BACKGROUND: We investigated the expression pattern of a human stem cell-specific, large intergenic noncoding RNA (lincRNA) regulator of reprogramming (lincRNA-ROR) and its spliced transcript variants in breast tumors. Breast cancer is the leading cause of cancer mortality in women; therefore, finding a reliable diagnostic tumor marker, based on the molecular profile of tumor cells, is warranted. METHODS: qRT-PCR was used to investigate the expression alteration of a specific stem cell-related lincRNA and its spliced transcript variants in breast tumors which provided by the Iran National Tumor Bank (2014–2016). Suitability of lincRNA-ROR and expression alterations of its spliced transcript variants as breast tumor biomarkers were examined by ROC curve analysis. RESULTS: Expression was significantly upregulated in lincRNA-ROR variants 1 (NR-048536) and 4 (AB844432) and downregulated in variant 3 (AB844431), with expression levels failing to distinguish between breast tumor types, grades, and malignancy stages. Whereas ROC curve analysis gave good scores to the expressions of variants 1 (AUC=0.7675, P=0.003) and 3 (AUC=0.9383, P=0.00173), suggesting their suitability as potential breast tumor biomarkers, it gave an AUC score of 0.6033 for lincRNA-ROR spliced variant 4 (P=0.4118), denoting its unsuitability as a breast cancer biomarker. CONCLUSION: Aberrant expressions of lincRNA-ROR spliced transcript variants could serve as reliable biomarkers with potential usefulness in breast cancer diagnosis. However, further research should elucidate the role and tissue expression of lincRNA-ROR spliced transcript variants in various cancers.
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spelling pubmed-101135672023-04-20 Differential Expression of lincRNA-ROR Spliced Transcript Variants in Breast Cancer Saadat Akhtar, Mozhgan Gholipour, Akram Bagheri Moghaddam, Mahrokh Oveisee, Maziar Mowla, Seyed Javad Malakootian, Mahshid Iran J Public Health Original Article BACKGROUND: We investigated the expression pattern of a human stem cell-specific, large intergenic noncoding RNA (lincRNA) regulator of reprogramming (lincRNA-ROR) and its spliced transcript variants in breast tumors. Breast cancer is the leading cause of cancer mortality in women; therefore, finding a reliable diagnostic tumor marker, based on the molecular profile of tumor cells, is warranted. METHODS: qRT-PCR was used to investigate the expression alteration of a specific stem cell-related lincRNA and its spliced transcript variants in breast tumors which provided by the Iran National Tumor Bank (2014–2016). Suitability of lincRNA-ROR and expression alterations of its spliced transcript variants as breast tumor biomarkers were examined by ROC curve analysis. RESULTS: Expression was significantly upregulated in lincRNA-ROR variants 1 (NR-048536) and 4 (AB844432) and downregulated in variant 3 (AB844431), with expression levels failing to distinguish between breast tumor types, grades, and malignancy stages. Whereas ROC curve analysis gave good scores to the expressions of variants 1 (AUC=0.7675, P=0.003) and 3 (AUC=0.9383, P=0.00173), suggesting their suitability as potential breast tumor biomarkers, it gave an AUC score of 0.6033 for lincRNA-ROR spliced variant 4 (P=0.4118), denoting its unsuitability as a breast cancer biomarker. CONCLUSION: Aberrant expressions of lincRNA-ROR spliced transcript variants could serve as reliable biomarkers with potential usefulness in breast cancer diagnosis. However, further research should elucidate the role and tissue expression of lincRNA-ROR spliced transcript variants in various cancers. Tehran University of Medical Sciences 2023-02 /pmc/articles/PMC10113567/ /pubmed/37089151 http://dx.doi.org/10.18502/ijph.v52i2.11896 Text en Copyright © 2023 Saadat Akhtar et al. Published by Tehran University of Medical Sciences https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Original Article
Saadat Akhtar, Mozhgan
Gholipour, Akram
Bagheri Moghaddam, Mahrokh
Oveisee, Maziar
Mowla, Seyed Javad
Malakootian, Mahshid
Differential Expression of lincRNA-ROR Spliced Transcript Variants in Breast Cancer
title Differential Expression of lincRNA-ROR Spliced Transcript Variants in Breast Cancer
title_full Differential Expression of lincRNA-ROR Spliced Transcript Variants in Breast Cancer
title_fullStr Differential Expression of lincRNA-ROR Spliced Transcript Variants in Breast Cancer
title_full_unstemmed Differential Expression of lincRNA-ROR Spliced Transcript Variants in Breast Cancer
title_short Differential Expression of lincRNA-ROR Spliced Transcript Variants in Breast Cancer
title_sort differential expression of lincrna-ror spliced transcript variants in breast cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113567/
https://www.ncbi.nlm.nih.gov/pubmed/37089151
http://dx.doi.org/10.18502/ijph.v52i2.11896
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