» Articles » PMID: 30301137

Peroxiredoxins in Colorectal Cancer: Predictive Biomarkers of Radiation Response and Therapeutic Targets to Increase Radiation Sensitivity?

Overview
Date 2018 Oct 11
PMID 30301137
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Colorectal cancer (CRC) is the third most common cancer in the Western world, with one-third of cases located in the rectum. Preoperative radiotherapy is the standard of care for many patients with rectal cancer but has a highly variable response rate. The ability to predict response would be of great clinical utility. The response of cells to ionizing radiation is known to involve immediate damage to biomolecules and more sustained disruption of redox homeostasis leading to cell death. The peroxiredoxins are an important group of thiol-dependent antioxidants involved in protecting cells from oxidative stress and regulating signaling pathways involved in cellular responses to oxidative stress. All six human peroxiredoxins have shown increased expression in CRC and may be associated with clinicopathological features and tumor response to ionizing radiation. Peroxiredoxins can act as markers of oxidative stress in various biological systems but they have not been investigated in this capacity in CRC. As such, there is currently insufficient evidence to support the role of peroxiredoxins as clinical biomarkers, but it is an area worthy of investigation. Future research should focus on the in vivo response of rectal cancer to radiotherapy and the redox status of peroxiredoxins in rectal cancer cells, in order to predict response to radiotherapy. The peroxiredoxin system is also a potential therapeutic target for CRC.

Citing Articles

Disruption of Colorectal Cancer Network by Polyphyllins Reveals Pivotal Entities with Implications for Chemoimmunotherapy.

Siripuram R, Bartolek Z, Patil K, Gill S, Pai S Biomedicines. 2022; 10(3).

PMID: 35327385 PMC: 8945690. DOI: 10.3390/biomedicines10030583.


Identification of potential metabolic biomarkers of rectal cancer and of the effect of neoadjuvant radiochemotherapy.

Rodriguez-Tomas E, Arenas M, Gomez J, Acosta J, Trilla J, Lopez Y PLoS One. 2021; 16(4):e0250453.

PMID: 33886674 PMC: 8062076. DOI: 10.1371/journal.pone.0250453.


Preventing Colitis-Associated Colon Cancer With Antioxidants: A Systematic Review.

Irrazabal T, Thakur B, Croitoru K, Martin A Cell Mol Gastroenterol Hepatol. 2021; 11(4):1177-1197.

PMID: 33418102 PMC: 7907812. DOI: 10.1016/j.jcmgh.2020.12.013.


Kinetic modeling of H2O2 dynamics in the mitochondria of HeLa cells.

Stein K, Moon S, Nguyen A, Sikes H PLoS Comput Biol. 2020; 16(9):e1008202.

PMID: 32925922 PMC: 7515204. DOI: 10.1371/journal.pcbi.1008202.

References
1.
Huang B, Langford T, Sikes H . Using Sensors and Generators of H2O2 to Elucidate the Toxicity Mechanism of Piperlongumine and Phenethyl Isothiocyanate. Antioxid Redox Signal. 2016; 24(16):924-38. PMC: 4900193. DOI: 10.1089/ars.2015.6482. View

2.
Anderson S, Bankier A, Barrell B, de Bruijn M, Coulson A, Drouin J . Sequence and organization of the human mitochondrial genome. Nature. 1981; 290(5806):457-65. DOI: 10.1038/290457a0. View

3.
Yi N, Xiao M, Ni W, Jiang F, Lu C, Ni R . High expression of peroxiredoxin 4 affects the survival time of colorectal cancer patients, but is not an independent unfavorable prognostic factor. Mol Clin Oncol. 2014; 2(5):767-772. PMC: 4106752. DOI: 10.3892/mco.2014.317. View

4.
Sun J, Chen Y, Li M, Ge Z . Role of antioxidant enzymes on ionizing radiation resistance. Free Radic Biol Med. 1998; 24(4):586-93. DOI: 10.1016/s0891-5849(97)00291-8. View

5.
Zhang B, Wang Y, Liu K, Yang X, Song M, Wang Y . Adenovirus-mediated transfer of siRNA against peroxiredoxin I enhances the radiosensitivity of human intestinal cancer. Biochem Pharmacol. 2007; 75(3):660-7. DOI: 10.1016/j.bcp.2007.09.016. View