<HashMap><database>bioimages</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Andriy Trailin</submitter><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-BIAD2384</full_dataset_link><repository>bioimages</repository><figure_sub>Specimen</figure_sub><figure_sub>Image analysis</figure_sub><figure_sub>Funding</figure_sub><figure_sub>Study Component</figure_sub><figure_sub>Biosample</figure_sub><figure_sub>organisation</figure_sub><figure_sub>Associations</figure_sub><figure_sub>Annotation</figure_sub><figure_sub>Image acquisition</figure_sub><pubmed_authors>Andriy Trailin</pubmed_authors></additional><is_claimable>false</is_claimable><name>Distribution and prognostic value of T-cells in primary colorectal cancer and adjacent non-tumor mucosa in stage IV versus stage I-III patients</name><description>Analysing and comparing the counts and ratios of specific T-cell subsets in and between primary colorectal cancer (pCRC) and adjacent non-tumor mucosa (NM) may reveal distinct prognostic value in patients who already have liver metastases (LM) and those who develop them later.
Formalin-fixed paraffin-embedded specimens of pCRC and NM were collected retrospectively from stage IV patients (n=55) with synchronous LM, and stage I-III patients (n=44) who developed metachronous LM later. CD3⁺, CD8⁺, CD45RO⁺, CD4⁺, and Foxp3⁺ T-cells were stained immunohistochemically and quantified in NM and the tumor center (TC) of pCRC. T-cell densities in NM and TC as well as their ratios (TC/NM) were tested as prognostic variables for overall survival (OS). Foxp3⁺/CD8⁺, Foxp3⁺/CD4⁺ and CD4⁺/CD8⁺ ratios were also evaluated for their prognostic relevance. Cell densities in TC and NM of stage I-III patients were also tested for associations with the time to occurrence of liver metastases.
In both groups, NM exhibited greater densities of CD3⁺, CD8⁺, CD45RO⁺ and CD4⁺ cells compared to TC, whereas Foxp3⁺ cells were more abundant in the TC. In stage IV patients, high densities of Foxp3⁺ cells, high Foxp3⁺/CD4⁺ and Foxp3⁺/CD8⁺ cell ratios in the NM, and high CD4⁺ cell densities in the TC were associated with longer OS. Stage I-III patients with a high CD4⁺/CD8⁺ cell ratio in the NM had longer OS whereas a high Foxp3⁺/CD8⁺ cell ratio in the TC was associated with a significantly shorter time to the occurrence of LM. High CD4⁺ cell densities in the TC, high Foxp3⁺/CD4⁺ and Foxp3⁺/CD8⁺ cell ratios in the NM retained significant associations with OS in all multivariable models.
We revealed a significant difference in the T-cell landscape between pCRC and adjacent NM with Foxp3⁺ cells predominating in the TC and other subsets predominating in the NM regardless of the metastasis status. Additionally, the assessment of T-cells in the NM and pCRC, both individually and in ratios, may help predict survival in CRC patients and the time to occurrence of LM in stages I-III.

</description><dates><release>2026-02-01T00:00:00Z</release><modification>2026-05-03T18:00:35.64Z</modification><creation>2025-11-05T16:10:34.298Z</creation></dates><accession>S-BIAD2384</accession><cross_references/></HashMap>