ArticleBiomedicine & pharmacotherapy = Biomedecine & pharmacotherapie2026
Activation of an adaptive antitumor immune response by the polymeric fluoropyrimidine CF10 involves TS/Top1 dual targeting.
Article in Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
5-Fluorouracil (5-FU)-based regimens remain the backbone of therapy for metastatic colorectal cancer (mCRC), yet durable responses are rare.CF10, a next-generation polymeric fluoropyrimidine, has demonstrated superior antitumor activity compared with 5-FU in preclinical models. Here, we evaluated whether CF10 more effectively induces immunogenic cell death (ICD) and promotes antitumor immunity, while characterizing its dual mechanism involving thymidylate synthase (TS) inhibition and replication stress through Topoisomerase 1 cleavage complex (Top1cc) stabilization and γ-H2AX accumulation. In murine (MC38) and human (HCT116) colorectal cancer cells, CF10 induced significantly higher levels of ICD markers-extracellular ATP, HMGB1 release, and surface calreticulin-than 5-FU and triggered robust Top1cc stabilization with γ-H2AX foci formation. Conditioned media from CF10-treated cells enhanced dendritic cell (DC) maturation and secretion of TNF-α, IL-1β, CCL2, and CCL4. In vivo, CF10 treatment in C57BL/6 mice bearing orthotopic MC38 liver metastases increased CD4⁺, CD8⁺, and γδ T-cell infiltration, reduced myeloid-derived suppressor cells (MDSCs), and decreased hepatic tumor burden. CF10 also decreased FoxP3⁺ regulatory T cells and CD206⁺ immunosuppressive macrophages. DC vaccination using CF10-conditioned supernatants modestly extended survival and increased tumor-infiltrating T cells compared with 5-FU or untreated controls. CF10 elicits a dual-action mechanism-cytotoxicity via TS inhibition and Top1cc-dependent replication stress (γ-H2AX) and immunogenicity through ICD induction-driving potent DC activation and adaptive immune responses. These findings position CF10 as a promising immunomodulatory chemotherapeutic for mCRC and support clinical evaluation, including combination strategies with immune checkpoint blockade.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.