Title
Antitumor effects of curcumin: A lipid perspective
Date Issued
01 September 2019
Access level
metadata only access
Resource Type
review
Author(s)
Pontificia Universidad Javeriana
Publisher(s)
Wiley-Liss Inc.
Abstract
Lipid metabolism plays an important role in cancer development due to the necessities of rapidly dividing cells to increase structural, energetic, and biosynthetic demands for cell proliferation. Basically, obesity, type 2 diabetes, and other related diseases, and cancer are associated with a common hyperactivated “lipogenic state.” Recent evidence suggests that metabolic reprogramming and overproduction of enzymes involved in the synthesis of fatty acids are the new hallmarks of cancer, which occur in an early phase of tumorigenesis. As the first evidence to confirm dysregulated lipid metabolism in cancer cells, the overexpression of fatty acid synthase (FAS) was observed in breast cancer patients and demonstrated the role of FAS in cancer. Other enzymes of fatty acid synthesis have recently been found to be dysregulated in cancer, including ATP-dependent citrate lyase and acetyl-CoA carboxylase, which further underscores the connection of these metabolic pathways with cancer cell survival and proliferation. The degree of overexpression of lipogenic enzymes and elevated lipid utilization in tumors is closely associated with cancer progression. The question that arises is whether the progression of cancer can be suppressed, or at least decelerated, by modulating gene expression related to fatty acid metabolism. Curcumin, due to its effects on the regulation of lipogenic enzymes, might be able to suppress, or even cause regression of tumor growth. This review discusses recent evidence concerning the important role of lipogenic enzymes in the metabolism of cancer cells and whether the inhibitory effects of curcumin on lipogenic enzymes is therapeutically efficacious.
Start page
14743
End page
14758
Volume
234
Issue
9
Language
English
OCDE Knowledge area
Nutrición, Dietética
Oncología
Bioquímica, Biología molecular
Farmacología, Farmacia
Subjects
Scopus EID
2-s2.0-85061473903
Source
Journal of Cellular Physiology
ISSN of the container
00219541
Sources of information:
Directorio de Producción Científica
Scopus