The Concept behind the Suitability of Menstrual Blood-Derived Stem Cells for the Management of Vaginal Atrophy among BRCA Mutation Carriers after RRSO.
Mariana Robalo CordeiroBárbara LaranjeiroMargarida Figueiredo DiasPublished in: International journal of molecular sciences (2024)
Risk-reducing bilateral salpingo-oophorectomy (RRSO) is recommended for breast cancer gene 1 (BRCA1) and 2 (BRCA2) mutation carriers. A major consequence of RRSO is surgical menopause associated with severe menopausal symptoms, mostly genitourinary complaints. Due to the inherent breast cancer risk, estrogen-based therapies are generally avoided in these patients. So far, the non-hormonal approaches available are not efficient to successfully treat the disabling vaginal atrophy-related symptoms. In regenerative medicine, mesenchymal stem cells (MSC) are the most frequently used cell type due to their remarkable and regenerative characteristics. Therapies based on MSC have revealed positive outcomes regarding symptoms and signs associated with vaginal atrophy by promoting angiogenesis, vaginal restoration, and the proliferation of vaginal mucosa cells. Menstrual blood-derived stem cells (MenSC) are a novel source of MSC, with promising therapeutic potential directly linked to their high proliferative rates; low immunogenicity; non-invasive, easy, and periodic acquisition; and almost no associated ethical issues. In this review, we update the current knowledge and research regarding the potential value of previously preserved MenSC in the therapy of vaginal atrophy among BRCA mutation carriers subjected to RRSO.
Keyphrases
- breast cancer risk
- stem cells
- mesenchymal stem cells
- cell therapy
- end stage renal disease
- healthcare
- chronic kidney disease
- induced apoptosis
- ejection fraction
- newly diagnosed
- umbilical cord
- signaling pathway
- sleep quality
- prognostic factors
- type diabetes
- endoplasmic reticulum stress
- dna methylation
- postmenopausal women
- skeletal muscle
- weight loss
- replacement therapy
- patient reported
- climate change
- estrogen receptor
- physical activity
- risk assessment
- oxidative stress