Cited by 87Metabolism, Diabetes, and CancerCancer, Hypoxia, and MetabolismCancer Risks and Factors

Type 2 Diabetes and Breast Cancer: The Interplay Between Impaired Glucose Metabolism and Oxidant Stress

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Ferroni, Patrizia, Riondino, Silvia, Buonomo, Oreste, Palmirotta, Raffaele, Guadagni, Fiorella, Roselli, Mario·2015·Oxidative Medicine and Cellular Longevity

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.

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  • The metabolic changes that occur as a result of diabetes (hyperinsulinemia, hyperglycemia, and dyslipidemia) potentiate signaling pathways and may increase the oncogenic nature of breast tissue through accelerating cell growth and migration, angiogenesis, increasing metastasis, and decreasing the response to chemotherapy.

    “The metabolic changes that occur as a result of diabetes (hyperinsulinemia, hyperglycemia, and dyslipidemia) potentiate signaling pathways and may increase the oncogenic nature of breast tissue through accelerating cell growth and migration, angiogenesis, increasing metastasis, and decreasing the response to chemotherapy (158, 244–247).”

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References 102 · Cited by 87

Research works printed but not linked: 1

  1. [1]International Diabetes Federation IDF Diabetes Atlas 2014 6th http://www.idf.org/diabetesatlas/ 35914061

Authors
Ferroni, P., Riondino, S., Buonomo, O., Palmirotta, R., Guadagni, F., & Roselli, M.
Affiliations
  • San Raffaele University of Rome (IT)
  • University of Rome Tor Vergata (IT)
Corresponding author
Roselli, Mario
Venue
Oxidative Medicine and Cellular Longevity
Publisher
Wiley
Published
2015
Volume
2015
Pages
1-10
ISSN
  • 1942-0994 (ISSN-L)
  • 1942-0900
OpenAlex
W1489101985
Cited by
87
References
102
Citations by year
2026: 10 · 2025: 3 · 2024: 3 · 2023: 9 · 2022: 6 · 2021: 15 · 2020: 9 · 2019: 9 · 2018: 6 · 2017: 6 · 2016: 11
FWCI
0.74
Type
journal article
Language
en
Open access
Locations
  • Oxidative Medicine and Cellular Longevity (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Cineca Institutional Research Information System (Tor Vergata University) (submittedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
Italian Ministry of Education Universities and Research (MERIT RBNE08NKH7)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
  • Health Sciences › Medicine › Oncology › Cancer Risks and Factors
Keywords
type 2 diabetes, breast cancer, impaired glucose metabolism, oxidative stress, hyperinsulinemia, insulin resistance, chronic inflammation, reactive oxygen species, tumor progression, platelet activation, innate immune activation, proangiogenic cytokines, biomarkers
MeSH terms
Breast Neoplasms, Diabetes Mellitus, Type 2, Female, Glucose, Humans, Hypoglycemic Agents, Inflammation, Reactive Oxygen Species, Oxidative Stress, Mitogen-Activated Protein Kinases

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