Molecular Links between Central Obesity and Breast Cancer
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, přehledy
PubMed
31661891
PubMed Central
PMC6862548
DOI
10.3390/ijms20215364
PII: ijms20215364
Knihovny.cz E-zdroje
- Klíčová slova
- abdominal fat, adiponectin, breast cancer, exosomes, hormone dependency, leptin, menopause, miRNA, obesity,
- MeSH
- abdominální obezita komplikace metabolismus patofyziologie MeSH
- adiponektin škodlivé účinky metabolismus MeSH
- estrogeny škodlivé účinky metabolismus MeSH
- exozom metabolismus MeSH
- leptin imunologie metabolismus MeSH
- lidé MeSH
- menopauza metabolismus MeSH
- mikro RNA metabolismus MeSH
- nádorová transformace buněk metabolismus MeSH
- nádorové mikroprostředí imunologie MeSH
- nádory prsu etiologie metabolismus patofyziologie MeSH
- signální transdukce genetika MeSH
- tuková tkáň imunologie metabolismus MeSH
- zánět patofyziologie MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- adiponektin MeSH
- estrogeny MeSH
- exozom MeSH
- leptin MeSH
- mikro RNA MeSH
: Worldwide, breast cancer (BC) is the most common malignancy in women, in regard to incidence and mortality. In recent years, the negative role of obesity during BC development and progression has been made abundantly clear in several studies. However, the distribution of body fat may be more important to analyze than the overall body weight. In our review of literature, we reported some key findings regarding the role of obesity in BC development, but focused more on central adiposity. Firstly, the adipose microenvironment in obese people bears many similarities with the tumor microenvironment, in respect to associated cellular composition, chronic low-grade inflammation, and high ratio of reactive oxygen species to antioxidants. Secondly, the adipose tissue functions as an endocrine organ, which in obese people produces a high level of tumor-promoting hormones, such as leptin and estrogen, and a low level of the tumor suppressor hormone, adiponectin. As follows, in BC this leads to the activation of oncogenic signaling pathways: NFκB, JAK, STAT3, AKT. Moreover, overall obesity, but especially central obesity, promotes a systemic and local low grade chronic inflammation that further stimulates the increase of tumor-promoting oxidative stress. Lastly, there is a constant exchange of information between BC cells and adipocytes, mediated especially by extracellular vesicles, and which changes the transcription profile of both cell types to an oncogenic one with the help of regulatory non-coding RNAs.
Central European Institute of Technology Masaryk University 62100 Brno Czech Republic
Masaryk Memorial Cancer Institute Department of Comprehensive Cancer Care 60200 Brno Czech Republic
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