ArticleFrontiers in oncology2026
IFI44L modulates chemoradiotherapy sensitivity and CD8
Article in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Objective: Chemoradiotherapy (CRT) represents a cornerstone treatment for colorectal cancer (CRC), yet heterogeneous responses to CRT in treatment response remain a major clinical challenge. Increasing evidence suggests that the tumor immune microenvironment (TME) especially intratumoral CD8 Methods: Transcriptomic profiling of rectal cancer cohorts was performed to identify genes associated with CRT response, followed by pathway enrichment analyses to explore potential biological mechanisms. The functional role of interferon-induced protein 44-like (IFI44L) was investigated using Results: IFI44L is identified as a candidate gene associated with CRT response through multi-cohort transcriptomic analysis. IFI44L overexpression did not directly alter CRC cell proliferation or CRT response Conclusions: Our findings identify IFI44L as an immune-dependent regulator of CRT sensitivity in CRC. By promoting CCL5-mediated CD8
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