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Background <p>Colorectal cancer (CRC) remains a significant clinical challenge. Immunotherapy against programmed cell death 1 protein (PD-1) in CRC has limited success. Intriguingly, CRC cells express PD-1 (ciPD-1) intrinsically, and we report here its function with respect to chemotherapy.</p> Methods <p>We evaluated the associations between ciPD-1 expression and disease progression, overall survival, and upregulation of survival pathways in human CRC tumors. Expression levels of ciPD-1 in CRC cells were modulated to evaluate its biological role in vitro.</p> Results <p>High expression levels of PD-1 in CRC tumors are associated with inferior outcomes; these tumors are also more aggressive and drug-resistant. Expression levels of ciPD-1 in CRC cells increase during 5-FU or CPT-11 treatment and are accompanied by upregulation of cell survival pathways. When ciPD-1 is inhibited, the cell-killing effects of 5-FU or CPT-11 were significantly increased. Our data show that ciPD-1 signaling occurs via MAPK signaling in CRC cells to support survival under stress conditions.</p> Conclusions <p>CRC tumors with high levels of ciPD-1 are more aggressive and associated with inferior outcomes. Reducing ciPD-1 levels in CRC cells make them more sensitive to chemotherapy. The aggregate results suggest that using a PD-1 inhibitor with first-line treatments in CRC could improve therapeutic efficacy.</p> <p></p>

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Tumor cell-intrinsic PD-1 regulates chemotherapy resistance in colorectal cancer cells by activating downstream MAPK signaling

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年11月19日

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  • Ho Kit Mok,
  • Sophie Sneddon,
  • Jianhua Ren,
  • Donald T. T. Yapp,
  • Isabella T. Tai

摘要

Background

Colorectal cancer (CRC) remains a significant clinical challenge. Immunotherapy against programmed cell death 1 protein (PD-1) in CRC has limited success. Intriguingly, CRC cells express PD-1 (ciPD-1) intrinsically, and we report here its function with respect to chemotherapy.

Methods

We evaluated the associations between ciPD-1 expression and disease progression, overall survival, and upregulation of survival pathways in human CRC tumors. Expression levels of ciPD-1 in CRC cells were modulated to evaluate its biological role in vitro.

Results

High expression levels of PD-1 in CRC tumors are associated with inferior outcomes; these tumors are also more aggressive and drug-resistant. Expression levels of ciPD-1 in CRC cells increase during 5-FU or CPT-11 treatment and are accompanied by upregulation of cell survival pathways. When ciPD-1 is inhibited, the cell-killing effects of 5-FU or CPT-11 were significantly increased. Our data show that ciPD-1 signaling occurs via MAPK signaling in CRC cells to support survival under stress conditions.

Conclusions

CRC tumors with high levels of ciPD-1 are more aggressive and associated with inferior outcomes. Reducing ciPD-1 levels in CRC cells make them more sensitive to chemotherapy. The aggregate results suggest that using a PD-1 inhibitor with first-line treatments in CRC could improve therapeutic efficacy.