From Micro to Long: Non-Coding RNAs in Tamoxifen Resistance of Breast Cancer Cells.

breast cancer endocrine resistance estrogen receptor lncRNA microRNA ncRNA tamoxifen

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
22 Jul 2021
Historique:
received: 31 03 2021
revised: 03 07 2021
accepted: 15 07 2021
entrez: 7 8 2021
pubmed: 8 8 2021
medline: 8 8 2021
Statut: epublish

Résumé

Breast cancer is the most commonly diagnosed cancer and the leading cause of cancer mortality among women. Two thirds of patients are classified as hormone receptor positive, based on expression of estrogen receptor alpha (ERα), the main driver of breast cancer cell proliferation, and/or progesterone receptor, which is regulated by ERα. Despite presenting the best prognosis, these tumors can recur when patients acquire resistance to treatment by aromatase inhibitors or antiestrogen such as tamoxifen (Tam). The mechanisms that are involved in Tam resistance are complex and involve multiple signaling pathways. Recently, roles for microRNAs and lncRNAs in controlling ER expression and/or tamoxifen action have been described, but the underlying mechanisms are still little explored. In this review, we will discuss the current state of knowledge on the roles of microRNAs and lncRNAs in the main mechanisms of tamoxifen resistance in hormone receptor positive breast cancer. In the future, this knowledge can be used to identify patients at a greater risk of relapse due to the expression patterns of ncRNAs that impact response to Tam, in order to guide their treatment more efficiently and possibly to design therapeutic strategies to bypass mechanisms of resistance.

Identifiants

pubmed: 34359587
pii: cancers13153688
doi: 10.3390/cancers13153688
pmc: PMC8345104
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Jéssica Fernanda Barazetti (JF)

Post-Graduation Program in Genetics, Department of Genetics, Federal University of Parana, Curitiba 81530-000, Parana, Brazil.

Tayana Shultz Jucoski (TS)

Post-Graduation Program in Genetics, Department of Genetics, Federal University of Parana, Curitiba 81530-000, Parana, Brazil.

Tamyres Mingorance Carvalho (TM)

Post-Graduation Program in Genetics, Department of Genetics, Federal University of Parana, Curitiba 81530-000, Parana, Brazil.

Rafaela Nasser Veiga (RN)

Post-Graduation Program in Genetics, Department of Genetics, Federal University of Parana, Curitiba 81530-000, Parana, Brazil.

Ana Flávia Kohler (AF)

Post-Graduation Program in Genetics, Department of Genetics, Federal University of Parana, Curitiba 81530-000, Parana, Brazil.

Jumanah Baig (J)

Department of Biochemistry and Molecular Medicine, University of Montreal, Montreal, QC H3T 1J4, Canada.
Institute for Research in Immunology and Cancer, University of Montreal, Montreal, QC H3T 1J4, Canada.

Hend Al Bizri (H)

Department of Biochemistry and Molecular Medicine, University of Montreal, Montreal, QC H3T 1J4, Canada.

Daniela Fiori Gradia (DF)

Post-Graduation Program in Genetics, Department of Genetics, Federal University of Parana, Curitiba 81530-000, Parana, Brazil.

Sylvie Mader (S)

Department of Biochemistry and Molecular Medicine, University of Montreal, Montreal, QC H3T 1J4, Canada.
Institute for Research in Immunology and Cancer, University of Montreal, Montreal, QC H3T 1J4, Canada.

Jaqueline Carvalho de Oliveira (J)

Post-Graduation Program in Genetics, Department of Genetics, Federal University of Parana, Curitiba 81530-000, Parana, Brazil.

Classifications MeSH