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Heme Oxygenase-1 and Its Role in Colorectal Cancer.

作者信息

Fahrer Jörg, Wittmann Simon, Wolf Ann-Cathrin, Kostka Tina

机构信息

Division of Food Chemistry and Toxicology, Department of Chemistry, RPTU Kaiserslautern-Landau, Erwin-Schrödinger Strasse 52, D-67663 Kaiserslautern, Germany.

出版信息

Antioxidants (Basel). 2023 Nov 10;12(11):1989. doi: 10.3390/antiox12111989.


DOI:10.3390/antiox12111989
PMID:38001842
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10669411/
Abstract

Heme oxygenase-1 (HO-1) is an enzyme located at the endoplasmic reticulum, which is responsible for the degradation of cellular heme into ferrous iron, carbon monoxide and biliverdin-IXa. In addition to this main function, the enzyme is involved in many other homeostatic, toxic and cancer-related mechanisms. In this review, we first summarize the importance of HO-1 in physiology and pathophysiology with a focus on the digestive system. We then detail its structure and function, followed by a section on the regulatory mechanisms that control HO-1 expression and activity. Moreover, HO-2 as important further HO isoform is discussed, highlighting the similarities and differences with regard to HO-1. Subsequently, we describe the direct and indirect cytoprotective functions of HO-1 and its breakdown products carbon monoxide and biliverdin-IXa, but also highlight possible pro-inflammatory effects. Finally, we address the role of HO-1 in cancer with a particular focus on colorectal cancer. Here, relevant pathways and mechanisms are presented, through which HO-1 impacts tumor induction and tumor progression. These include oxidative stress and DNA damage, ferroptosis, cell cycle progression and apoptosis as well as migration, proliferation, and epithelial-mesenchymal transition.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/5a45af05d18f/antioxidants-12-01989-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/6c668244b652/antioxidants-12-01989-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/7f1768a1980a/antioxidants-12-01989-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/b659fe3c1e79/antioxidants-12-01989-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/a391220ee34f/antioxidants-12-01989-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/730beb45b4d3/antioxidants-12-01989-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/93b47e397776/antioxidants-12-01989-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/5a45af05d18f/antioxidants-12-01989-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/6c668244b652/antioxidants-12-01989-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/7f1768a1980a/antioxidants-12-01989-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/b659fe3c1e79/antioxidants-12-01989-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/a391220ee34f/antioxidants-12-01989-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/730beb45b4d3/antioxidants-12-01989-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/93b47e397776/antioxidants-12-01989-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/10669411/5a45af05d18f/antioxidants-12-01989-g007.jpg

相似文献

[1]
Heme Oxygenase-1 and Its Role in Colorectal Cancer.

Antioxidants (Basel). 2023-11-10

[2]
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[3]
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[7]
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引用本文的文献

[1]
The Regulation of Trace Metal Elements in Cancer Ferroptosis.

Adv Biol (Weinh). 2025-8

[2]
The Heme Oxygenase/Biliverdin Reductase System and Its Genetic Variants in Physiology and Diseases.

Antioxidants (Basel). 2025-2-6

[3]
Influence of Mesalazine on Ferroptosis-Related Gene Expression in In Vitro Colorectal Cancer Culture.

Biomedicines. 2025-1-16

[4]
New Insights into Aspirin's Anticancer Activity: The Predominant Role of Its Iron-Chelating Antioxidant Metabolites.

Antioxidants (Basel). 2024-12-29

[5]
Mechanism of Action and Therapeutic Implications of Nrf2/HO-1 in Inflammatory Bowel Disease.

Antioxidants (Basel). 2024-8-20

[6]
Targeting ferroptosis as a potential strategy to overcome the resistance of cisplatin in oral squamous cell carcinoma.

Front Pharmacol. 2024-4-22

[7]
Putative Molecular Mechanisms Underpinning the Inverse Roles of Mitochondrial Respiration and Heme Function in Lung Cancer and Alzheimer's Disease.

Biology (Basel). 2024-3-14

本文引用的文献

[1]
Therapeutic inhibition of ferroptosis in neurodegenerative disease.

Trends Pharmacol Sci. 2023-10

[2]
New approach methodologies to facilitate and improve the hazard assessment of non-genotoxic carcinogens-a PARC project.

Front Toxicol. 2023-7-10

[3]
Proteomic analysis of the effect of hemin in breast cancer.

Sci Rep. 2023-6-21

[4]
Young-onset colorectal cancer.

Nat Rev Dis Primers. 2023-4-27

[5]
Role of ferroptosis in colorectal cancer.

World J Gastrointest Oncol. 2023-2-15

[6]
DNA Alkylation Damage by Nitrosamines and Relevant DNA Repair Pathways.

Int J Mol Sci. 2023-2-28

[7]
Heme induces intestinal epithelial cell ferroptosis via mitochondrial dysfunction in transfusion-associated necrotizing enterocolitis.

FASEB J. 2022-12

[8]
Role of Heme Oxygenase in Gastrointestinal Epithelial Cells.

Antioxidants (Basel). 2022-7-5

[9]
Epithelial de-differentiation triggered by co-ordinate epigenetic inactivation of the EHF and CDX1 transcription factors drives colorectal cancer progression.

Cell Death Differ. 2022-11

[10]
Hemin mitigates contrast-induced nephropathy by inhibiting ferroptosis via HO-1/Nrf2/GPX4 pathway.

Clin Exp Pharmacol Physiol. 2022-8

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