Biological Role and Clinical Implications of microRNAs in BRCA Mutation Carriers

Women with pathogenic germline mutations in BRCA1 and BRCA2 genes have an increased risk to develop breast and ovarian cancer. There is, however, a high interpersonal variability in the modality and timing of tumor onset in those subjects, thus suggesting a potential role of other individual’s genet...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in oncology Vol. 11; p. 700853
Main Authors Tommasi, Chiara, Pellegrino, Benedetta, Boggiani, Daniela, Sikokis, Angelica, Michiara, Maria, Uliana, Vera, Bortesi, Beatrice, Bonatti, Francesco, Mozzoni, Paola, Pinelli, Silvana, Squadrilli, Anna, Viani, Maria Vittoria, Cassi, Diana, Maglietta, Giuseppe, Meleti, Marco, Musolino, Antonino
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 06.09.2021
Subjects
Online AccessGet full text
ISSN2234-943X
2234-943X
DOI10.3389/fonc.2021.700853

Cover

Loading…
More Information
Summary:Women with pathogenic germline mutations in BRCA1 and BRCA2 genes have an increased risk to develop breast and ovarian cancer. There is, however, a high interpersonal variability in the modality and timing of tumor onset in those subjects, thus suggesting a potential role of other individual’s genetic, epigenetic, and environmental risk factors in modulating the penetrance of BRCA mutations. MicroRNAs (miRNAs) are small noncoding RNAs that can modulate the expression of several genes involved in cancer initiation and progression. MiRNAs are dysregulated at all stages of breast cancer and although they are accessible and evaluable, a standardized method for miRNA assessment is needed to ensure comparable data analysis and accuracy of results. The aim of this review was to highlight the role of miRNAs as potential biological markers for BRCA mutation carriers. In particular, biological and clinical implications of a link between lifestyle and nutritional modifiable factors, miRNA expression and germline BRCA1 and BRCA2 mutations are discussed with the knowledge of the best available scientific evidence.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
ObjectType-Review-3
content type line 23
Reviewed by: Bryan Raymond George Williams, Hudson Institute of Medical Research, Australia; Saeed Pirouzpanah, Tabriz University of Medical Sciences, Iran
This article was submitted to Cancer Genetics, a section of the journal Frontiers in Oncology
Edited by: Naoyuki Kataoka, The University of Tokyo, Japan
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2021.700853