ArticleCancer medicine2026
High SIGLEC10-Expressing Tumor-Associated Macrophages Participate in Remodeling the Tumor Immune Microenvironment and Predict Poor Prognosis in Colorectal Cancer.
Article in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
- Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
backgroundSialic acid-binding immunoglobulin-like lectin 10 (SIGLEC10), a member of the SIGLEC family, is selectively expressed on multiple immune cell subsets and plays a key role in immune regulation through the recognition of sialylated ligands. Recent studies suggest that SIGLEC10 functions as an emerging immune checkpoint that contributes to the regulation of tumor-associated macrophages (TAMs) within the tumor microenvironment (TME).
methodsImmunohistochemistry was performed to assess SIGLEC10 expression in a CRC cohort comprising 202 patients, and the association between SIGLEC10 expression and patient survival and prognosis was evaluated. Immunofluorescence staining and flow cytometry were used to characterize the localization and phenotypic features of SIGLEC10-expressing cells within tumor tissues. The Cancer Genome Atlas (TCGA) and RNA sequencing (RNA-seq) datasets were analyzed to investigate SIGLEC10-associated tumor immune signaling pathways. Additionally, single-cell datasets from Tumor Immune Single-cell Hub 2 (TISCH2) were used to further investigate the regulatory mechanisms of SIGLEC10
resultsHigh SIGLEC10 expression predicts poor prognosis in CRC patients and serves as an independent prognostic factor. SIGLEC10 is predominantly expressed in CD68
conclusionThis study highlights SIGLEC10 as an independent prognostic factor in patients with CRC and its potential as a promising target for immunotherapy in CRC.
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.