» Articles » PMID: 38356721

Association Between Atopic Dermatitis and Colorectal Cancer: TET2 As a Shared Gene Signature and Prognostic Biomarker

Overview
Journal J Cancer
Specialty Oncology
Date 2024 Feb 15
PMID 38356721
Authors
Affiliations
Soon will be listed here.
Abstract

Recent studies have linked atopic dermatitis (AD) to colorectal cancer (CRC) risk. Their causality and potential molecular mechanisms remain unclear. We performed Mendelian randomization (MR) analysis to evaluate the causality between AD and CRC. Summary statistic data-based Mendelian randomization (SMR) analysis was used to identify CRC-related causal genes. Transcriptome analyses and immunohistochemical methods were applied to investigate the shared gene signature and potential mechanisms that contribute to the pathogenesis of both AD and CRC. A predictive analysis was performed to examine the shared gene signature associated with immunotherapy response in CRC. MR analysis indicated a causal association between AD and a decreased risk of CRC. SMR analysis uncovered TET2 as a CRC-related causal gene, showing an inverse relationship with the risk of CRC. Transcriptome analyses identified TET2 as a shared gene signature between AD and CRC. Decreased TET2 expression is associated with impaired demethylation and worse prognosis in CRC patients. We observed ten pathways related to the inflammatory response and immune regulation that may be shared mechanisms underlying both AD and CRC. These findings were validated through single-cell analysis. TET2 shows promise as a powerful predictive biomarker for cancer prognosis and immunotherapy response in CRC. There is a causal association between AD and a decreased risk of CRC. AD may influence the occurrence of CRC by modulating immune and inflammatory responses. TET2 could serve as a potential biomarker for prognosis and may be considered a novel therapeutic target for methylation and immune-related interventions.

Citing Articles

Inflammasomes Are Influenced by Epigenetic and Autophagy Mechanisms in Colorectal Cancer Signaling.

Muzes G, Sipos F Int J Mol Sci. 2024; 25(11).

PMID: 38892354 PMC: 11173330. DOI: 10.3390/ijms25116167.

References
1.
Jacobs E, Gapstur S, Newton C, Turner M, Campbell P . Hay Fever and asthma as markers of atopic immune response and risk of colorectal cancer in three large cohort studies. Cancer Epidemiol Biomarkers Prev. 2013; 22(4):661-9. DOI: 10.1158/1055-9965.EPI-12-1229. View

2.
Shu Y, Cheng P . Targeting tumor-associated macrophages for cancer immunotherapy. Biochim Biophys Acta Rev Cancer. 2020; 1874(2):188434. DOI: 10.1016/j.bbcan.2020.188434. View

3.
Sung H, Ferlay J, Siegel R, Laversanne M, Soerjomataram I, Jemal A . Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin. 2021; 71(3):209-249. DOI: 10.3322/caac.21660. View

4.
Ubil E, Caskey L, Holtzhausen A, Hunter D, Story C, Earp H . Tumor-secreted Pros1 inhibits macrophage M1 polarization to reduce antitumor immune response. J Clin Invest. 2018; 128(6):2356-2369. PMC: 5983338. DOI: 10.1172/JCI97354. View

5.
Liu Q, Chen L, Wang Y, Wang X, Lewis S, Wang J . Atopic dermatitis and risk of 14 site-specific cancers: A Mendelian randomization study. J Eur Acad Dermatol Venereol. 2023; 37(12):2490-2497. DOI: 10.1111/jdv.19380. View