Abnormal Long Non-Coding RNAs Expression Patterns Have the Potential Ability for Predicting Survival and Treatment Response in Breast Cancer.


Journal

Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097

Informations de publication

Date de publication:
29 06 2021
Historique:
received: 18 05 2021
revised: 11 06 2021
accepted: 23 06 2021
entrez: 2 7 2021
pubmed: 3 7 2021
medline: 12 1 2022
Statut: epublish

Résumé

Abnormal long non-coding RNAs (lncRNAs) expression has been documented to have oncogene or tumor suppressor functions in the development and progression of cancer, emerging as promising independent biomarkers for molecular cancer stratification and patients' prognosis. Examining the relationship between lncRNAs and the survival rates in malignancies creates new scenarios for precision medicine and targeted therapy. Breast cancer (BRCA) is a heterogeneous malignancy. Despite advances in its molecular classification, there are still gaps to explain in its multifaceted presentations and a substantial lack of biomarkers that can better predict patients' prognosis in response to different therapeutic strategies. Here, we performed a re-analysis of gene expression data generated using cDNA microarrays in a previous study of our group, aiming to identify differentially expressed lncRNAs (DELncRNAs) with a potential predictive value for response to treatment with taxanes in breast cancer patients. Results revealed 157 DELncRNAs (90 up- and 67 down-regulated). We validated these new biomarkers as having prognostic and predictive value for breast cancer using in silico analysis in public databases. Data from TCGA showed that compared to normal tissue, MIAT was up-regulated, while KCNQ1OT1, LOC100270804, and FLJ10038 were down-regulated in breast tumor tissues. KCNQ1OT1, LOC100270804, and FLJ10038 median levels were found to be significantly higher in the luminal subtype. The ROC plotter platform results showed that reduced expression of these three DElncRNAs was associated with breast cancer patients who did not respond to taxane treatment. Kaplan-Meier survival analysis revealed that a lower expression of the selected lncRNAs was significantly associated with worse relapse-free survival (RFS) in breast cancer patients. Further validation of the expression of these DELncRNAs might be helpful to better tailor breast cancer prognosis and treatment.

Identifiants

pubmed: 34209776
pii: genes12070996
doi: 10.3390/genes12070996
pmc: PMC8305383
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Biomarkers, Tumor 0
RNA, Long Noncoding 0
Docetaxel 15H5577CQD

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Ana Carolina Pavanelli (AC)

Discipline of Oncology, Department of Radiology and Oncology, Faculty of Medicine, University of São Paulo, São Paulo 01246-903, Brazil.
Center for Translational Research in Oncology, Cancer Institute of São Paulo, São Paulo 01246-903, Brazil.

Flavia Rotea Mangone (FR)

Discipline of Oncology, Department of Radiology and Oncology, Faculty of Medicine, University of São Paulo, São Paulo 01246-903, Brazil.
Center for Translational Research in Oncology, Cancer Institute of São Paulo, São Paulo 01246-903, Brazil.

Luciana R C Barros (LRC)

Discipline of Oncology, Department of Radiology and Oncology, Faculty of Medicine, University of São Paulo, São Paulo 01246-903, Brazil.
Center for Translational Research in Oncology, Cancer Institute of São Paulo, São Paulo 01246-903, Brazil.

Juliana Machado-Rugolo (J)

Department of Pathology, University of São Paulo Medical School (USP), São Paulo 01246-903, Brazil.
Health Technology Assessment Center (NATS), Clinical Hospital (HCFMB), Medical School of São Paulo State University (UNESP), Botucatu, São Paulo 01246-903, Brazil.

Vera L Capelozzi (VL)

Department of Pathology, University of São Paulo Medical School (USP), São Paulo 01246-903, Brazil.

Maria A Nagai (MA)

Discipline of Oncology, Department of Radiology and Oncology, Faculty of Medicine, University of São Paulo, São Paulo 01246-903, Brazil.
Center for Translational Research in Oncology, Cancer Institute of São Paulo, São Paulo 01246-903, Brazil.

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Classifications MeSH