Redox and metabolic reprogramming in breast cancer and cancer‐associated adipose tissue

Redox and metabolic processes are tightly coupled in both physiological and pathological conditions. In cancer, their integration occurs at multiple levels and is characterized by synchronized reprogramming both in the tumor tissue and its specific but heterogeneous microenvironment. In breast cance...

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Published in:FEBS letters Vol. 598; no. 17; pp. 2106 - 2134
Main Authors: Zakic, Tamara, Pekovic‐Vaughan, Vanja, Cvoro, Aleksandra, Korac, Aleksandra, Jankovic, Aleksandra, Korac, Bato
Format: Journal Article
Language:English
Published: England 01.09.2024
Subjects:
adipose tissue
Adipose Tissue - metabolism
Adipose Tissue - pathology
Animals
breast cancer
breast neoplasms
Breast Neoplasms - metabolism
Breast Neoplasms - pathology
Cellular Reprogramming
Circadian Rhythm
circadian rhythms
estrogen
estrogens
Female
Humans
metabolic diseases
Metabolic Reprogramming
metabolism
Oxidation-Reduction
prognosis
Receptors, Estrogen - metabolism
redox‐metabolic reprogramming
therapeutics
Tumor Microenvironment
adipose tissue
breast cancer
estrogen
redox‐metabolic reprogramming
tumor microenvironment
circadian rhythms
ISSN:0014-5793, 1873-3468, 1873-3468
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Abstract Redox and metabolic processes are tightly coupled in both physiological and pathological conditions. In cancer, their integration occurs at multiple levels and is characterized by synchronized reprogramming both in the tumor tissue and its specific but heterogeneous microenvironment. In breast cancer, the principal microenvironment is the cancer‐associated adipose tissue (CAAT). Understanding how the redox‐metabolic reprogramming becomes coordinated in human breast cancer is imperative both for cancer prevention and for the establishment of new therapeutic approaches. This review aims to provide an overview of the current knowledge of the redox profiles and regulation of intermediary metabolism in breast cancer while considering the tumor and CAAT of breast cancer as a unique Warburg's pseudo‐organ. As cancer is now recognized as a systemic metabolic disease, we have paid particular attention to the cell‐specific redox‐metabolic reprogramming and the roles of estrogen receptors and circadian rhythms, as well as their crosstalk in the development, growth, progression, and prognosis of breast cancer. This review focuses on deciphering the redox and metabolic profiles of breast cancer and associated adipose tissue as a part of a unique Warburg pseudo‐organ. In the light of the coupled cancer and adipose tissue redox‐metabolic reprogramming, mechanistic links to estrogen receptors, tumor microenvironment cell heterogeneity, inflammation, and circadian rhythms as important players affecting breast cancer development, progression, and prognosis are also discussed (Created with BioRender.com).
AbstractList Redox and metabolic processes are tightly coupled in both physiological and pathological conditions. In cancer, their integration occurs at multiple levels and is characterized by synchronized reprogramming both in the tumor tissue and its specific but heterogeneous microenvironment. In breast cancer, the principal microenvironment is the cancer‐associated adipose tissue (CAAT). Understanding how the redox‐metabolic reprogramming becomes coordinated in human breast cancer is imperative both for cancer prevention and for the establishment of new therapeutic approaches. This review aims to provide an overview of the current knowledge of the redox profiles and regulation of intermediary metabolism in breast cancer while considering the tumor and CAAT of breast cancer as a unique Warburg's pseudo‐organ. As cancer is now recognized as a systemic metabolic disease, we have paid particular attention to the cell‐specific redox‐metabolic reprogramming and the roles of estrogen receptors and circadian rhythms, as well as their crosstalk in the development, growth, progression, and prognosis of breast cancer.
Redox and metabolic processes are tightly coupled in both physiological and pathological conditions. In cancer, their integration occurs at multiple levels and is characterized by synchronized reprogramming both in the tumor tissue and its specific but heterogeneous microenvironment. In breast cancer, the principal microenvironment is the cancer-associated adipose tissue (CAAT). Understanding how the redox-metabolic reprogramming becomes coordinated in human breast cancer is imperative both for cancer prevention and for the establishment of new therapeutic approaches. This review aims to provide an overview of the current knowledge of the redox profiles and regulation of intermediary metabolism in breast cancer while considering the tumor and CAAT of breast cancer as a unique Warburg's pseudo-organ. As cancer is now recognized as a systemic metabolic disease, we have paid particular attention to the cell-specific redox-metabolic reprogramming and the roles of estrogen receptors and circadian rhythms, as well as their crosstalk in the development, growth, progression, and prognosis of breast cancer.Redox and metabolic processes are tightly coupled in both physiological and pathological conditions. In cancer, their integration occurs at multiple levels and is characterized by synchronized reprogramming both in the tumor tissue and its specific but heterogeneous microenvironment. In breast cancer, the principal microenvironment is the cancer-associated adipose tissue (CAAT). Understanding how the redox-metabolic reprogramming becomes coordinated in human breast cancer is imperative both for cancer prevention and for the establishment of new therapeutic approaches. This review aims to provide an overview of the current knowledge of the redox profiles and regulation of intermediary metabolism in breast cancer while considering the tumor and CAAT of breast cancer as a unique Warburg's pseudo-organ. As cancer is now recognized as a systemic metabolic disease, we have paid particular attention to the cell-specific redox-metabolic reprogramming and the roles of estrogen receptors and circadian rhythms, as well as their crosstalk in the development, growth, progression, and prognosis of breast cancer.
Redox and metabolic processes are tightly coupled in both physiological and pathological conditions. In cancer, their integration occurs at multiple levels and is characterized by synchronized reprogramming both in the tumor tissue and its specific but heterogeneous microenvironment. In breast cancer, the principal microenvironment is the cancer‐associated adipose tissue (CAAT). Understanding how the redox‐metabolic reprogramming becomes coordinated in human breast cancer is imperative both for cancer prevention and for the establishment of new therapeutic approaches. This review aims to provide an overview of the current knowledge of the redox profiles and regulation of intermediary metabolism in breast cancer while considering the tumor and CAAT of breast cancer as a unique Warburg's pseudo‐organ. As cancer is now recognized as a systemic metabolic disease, we have paid particular attention to the cell‐specific redox‐metabolic reprogramming and the roles of estrogen receptors and circadian rhythms, as well as their crosstalk in the development, growth, progression, and prognosis of breast cancer. This review focuses on deciphering the redox and metabolic profiles of breast cancer and associated adipose tissue as a part of a unique Warburg pseudo‐organ. In the light of the coupled cancer and adipose tissue redox‐metabolic reprogramming, mechanistic links to estrogen receptors, tumor microenvironment cell heterogeneity, inflammation, and circadian rhythms as important players affecting breast cancer development, progression, and prognosis are also discussed (Created with BioRender.com).
Author Korac, Aleksandra
Jankovic, Aleksandra
Korac, Bato
Zakic, Tamara
Cvoro, Aleksandra
Pekovic‐Vaughan, Vanja
Author_xml – sequence: 1
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  surname: Zakic
  fullname: Zakic, Tamara
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  fullname: Pekovic‐Vaughan, Vanja
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  surname: Cvoro
  fullname: Cvoro, Aleksandra
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  givenname: Aleksandra
  surname: Korac
  fullname: Korac, Aleksandra
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  givenname: Aleksandra
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  surname: Korac
  fullname: Korac, Bato
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  organization: University of Belgrade
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CitedBy_id crossref_primary_10_3390_cells13050441
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IngestDate Sat Sep 27 17:09:42 EDT 2025
Sat Sep 27 20:58:24 EDT 2025
Mon Jul 21 05:52:39 EDT 2025
Tue Nov 18 22:16:32 EST 2025
Sat Nov 29 07:37:50 EST 2025
Wed Jan 22 17:14:12 EST 2025
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Issue 17
Keywords adipose tissue
breast cancer
estrogen
redox‐metabolic reprogramming
tumor microenvironment
circadian rhythms
Language English
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Snippet Redox and metabolic processes are tightly coupled in both physiological and pathological conditions. In cancer, their integration occurs at multiple levels and...
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SubjectTerms adipose tissue
Adipose Tissue - metabolism
Adipose Tissue - pathology
Animals
breast cancer
breast neoplasms
Breast Neoplasms - metabolism
Breast Neoplasms - pathology
Cellular Reprogramming
Circadian Rhythm
circadian rhythms
estrogen
estrogens
Female
Humans
metabolic diseases
Metabolic Reprogramming
metabolism
Oxidation-Reduction
prognosis
Receptors, Estrogen - metabolism
redox‐metabolic reprogramming
therapeutics
Tumor Microenvironment
Title Redox and metabolic reprogramming in breast cancer and cancer‐associated adipose tissue
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https://www.ncbi.nlm.nih.gov/pubmed/38140817
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https://www.proquest.com/docview/3153807288
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