CD155 promotes the progression of colorectal cancer by restraining CD8+ T cells via the PI3K/AKT/NF-κB pathway

This study revealed that CD155 can promote the progression of colorectal cancer by regulating the PI3K / AKT-NF-κB pathway to promote the depletion of CD8<sup>+</sup> T cells and reduce their migration to the tumor microenvironment. CD155 may become an important prognostic biomarker and an effective target for colorectal cancer immunotherapy.

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Publication Details

Journal
Cancer Immunology Immunotherapy
Published
2025-02-01
DOI
https://doi.org/10.1007/s00262-025-03947-y
Citations
4
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
3.19

Funders

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article

CD155 promotes the progression of colorectal cancer by restraining CD8+ T cells via the PI3K/AKT/NF-κB pathway

Yiquan Li, Jiannan Ren, Rongpu Liang, Liting Liu et al.
4 citations
Cancer Immunology Immunotherapy
Immune Cell Function and Interaction
3.19
article

CD155 promotes the progression of colorectal cancer by restraining CD8+ T cells via the PI3K/AKT/NF-κB pathway

Yiquan Li, Jiannan Ren, Rongpu Liang, Liting Liu, Bo Wei, Dongbing Ding
article en
4 citations

Abstract

This study revealed that CD155 can promote the progression of colorectal cancer by regulating the PI3K / AKT-NF-κB pathway to promote the depletion of CD8<sup>+</sup> T cells and reduce their migration to the tumor microenvironment. CD155 may become an important prognostic biomarker and an effective target for colorectal cancer immunotherapy.

Cancer Immunology ImmunotherapyVol. 74(3)
Sun Yat-sen University (CN), Third Affiliated Hospital of Sun Yat-sen University (CN)
Natural Science Foundation of Guangdong Province, Basic and Applied Basic Research Foundation of Guangdong Province
Good health and well-being
Openalex Percentile: Top 9%
Immune Cell Function and Interaction
3.19
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CD155 promotes the progression of colorectal cancer by restraining CD8+ T cells via the PI3K/AKT/NF-κB pathway — Yiquan Li, Jiannan Ren, et al. · Cancer Immunology Immunotherapy (2025) | TGRS Research Map | TGRS