Metabolic disorders, especially type 2 diabetes and its associated complications, represent a growing public health problem. Epidemiological findings indicate a close relationship between diabetes and many types of cancer (including breast cancer risk), which regards not only the dysmetabolic condition, but also its underlying risk factors and therapeutic interventions. This review discusses the advances in understanding of the mechanisms linking metabolic disorders and breast cancer. Among the proposed mechanisms to explain such an association, a major role is played by the dysregulated glucose metabolism, which concurs with a chronic proinflammatory condition and an associated oxidative stress to promote tumour initiation and progression. As regards the altered glucose metabolism, hyperinsulinaemia, both endogenous due to insulin-resistance and drug-induced, appears to promote tumour cell growth through the involvement of innate immune activation, platelet activation, increased reactive oxygen species, exposure to protumorigenic and proangiogenic cytokines, and increased substrate availability to neoplastic cells. In this context, understanding the relationship between metabolic disorders and cancer is becoming imperative, and an accurate analysis of these associations could be used to identify biomarkers able to predict disease risk and/or prognosis and to help in the choice of proper evidence-based diagnostic and therapeutic protocols.

Ferroni, P., Riondino, S., Buonomo, O.c., Palmirotta, R., Guadagni, F., Roselli, M. (2015). Type 2 diabetes and breast cancer: The interplay between impaired glucose metabolism and oxidant stress. OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2015 [10.1155/2015/183928].

Type 2 diabetes and breast cancer: The interplay between impaired glucose metabolism and oxidant stress

Riondino, S;BUONOMO, ORESTE CLAUDIO;ROSELLI, MARIO
2015-01-01

Abstract

Metabolic disorders, especially type 2 diabetes and its associated complications, represent a growing public health problem. Epidemiological findings indicate a close relationship between diabetes and many types of cancer (including breast cancer risk), which regards not only the dysmetabolic condition, but also its underlying risk factors and therapeutic interventions. This review discusses the advances in understanding of the mechanisms linking metabolic disorders and breast cancer. Among the proposed mechanisms to explain such an association, a major role is played by the dysregulated glucose metabolism, which concurs with a chronic proinflammatory condition and an associated oxidative stress to promote tumour initiation and progression. As regards the altered glucose metabolism, hyperinsulinaemia, both endogenous due to insulin-resistance and drug-induced, appears to promote tumour cell growth through the involvement of innate immune activation, platelet activation, increased reactive oxygen species, exposure to protumorigenic and proangiogenic cytokines, and increased substrate availability to neoplastic cells. In this context, understanding the relationship between metabolic disorders and cancer is becoming imperative, and an accurate analysis of these associations could be used to identify biomarkers able to predict disease risk and/or prognosis and to help in the choice of proper evidence-based diagnostic and therapeutic protocols.
2015
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/06 - ONCOLOGIA MEDICA
English
Con Impact Factor ISI
Breast Neoplasms; Diabetes Mellitus, Type 2; Female; Glucose; Humans; Hypoglycemic Agents; Inflammation; Mitogen-Activated Protein Kinases; Reactive Oxygen Species; Oxidative Stress
Ferroni, P., Riondino, S., Buonomo, O.c., Palmirotta, R., Guadagni, F., Roselli, M. (2015). Type 2 diabetes and breast cancer: The interplay between impaired glucose metabolism and oxidant stress. OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2015 [10.1155/2015/183928].
Ferroni, P; Riondino, S; Buonomo, Oc; Palmirotta, R; Guadagni, F; Roselli, M
Articolo su rivista
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/147669
Citazioni
  • ???jsp.display-item.citation.pmc??? 33
  • Scopus 62
  • ???jsp.display-item.citation.isi??? 59
social impact