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...
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Published in | Frontiers in oncology Vol. 11; p. 700853 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Frontiers Media S.A
06.09.2021
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Subjects | |
Online Access | Get full text |
ISSN | 2234-943X 2234-943X |
DOI | 10.3389/fonc.2021.700853 |
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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. |
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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 |