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June 5, 20260 citations

Colon Adenocarcinoma Cell-Derived Galectins-1,3 Modulate Differentiation of CD4+ T Lymphocytes In Vitro.

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VPV S PoletikaGRG V ReingardtAKA V Kurnosenko

Key Points

  • This study aims to explore how galectin-1 and galectin-3 from colon adenocarcinoma cells influence CD4+ T lymphocyte differentiation.
  • Analyzed mRNA expression in peripheral blood mononuclear cells (PBMCs) co-cultured with COLO 201 cells.
  • Inhibited galectin-1 using OTX 008 and galectin-3 using GB1107, either separately or in combination.
  • Compared effects on gene expression of T-bet, RORC2, and FOXP3 in PBMCs from colorectal cancer patients and healthy donors.
  • Inhibition of galectin-1 increased TBX21 and RORC2 mRNA expression while reducing FOXP3 in both patient and healthy donor PBMCs.
  • Galectin-3 inhibition enhanced FOXP3 and reduced RORC2 expression in healthy donor PBMCs, but mirrored the effects of galectin-1 in patient-derived PBMCs.
  • Simultaneous inhibition of both galectins led to the most significant decrease in FOXP3 expression.

Abstract

We investigated how selective inhibition of galectin-1 and galectin-3 expressed by COLO 201 colorectal adenocarcinoma cells modulates CD4+ T lymphocyte differentiation in vitro. The mRNA expression levels of the transcription factors T-bet (TBX21), RORC2, and Foxp3 were analyzed in peripheral blood mononuclear cells (PBMCs) from colorectal cancer patients and healthy donors following co-culture with COLO 201 cells in the presence of galectin-1 inhibitor OTX 008, galectin-3 inhibitor GB1107, or both. Inhibition of galectin-1 in co-cultures increased TBX21 and RORC2 mRNA expression while suppressing FOXP3 in PBMCs from both groups. In patient-derived PBMCs, galectin-3 inhibition produced a similar effect. Conversely, in healthy donor cells, galectin-3 blockade suppressed RORC2 and induced FOXP3 expression. Notably, the most pronounced downregulation of FOXP3 was achieved by simultaneously inhibiting both galectins.

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Cite This Study

Poletika et al. (2026) studied this question.

synapsesocial.com/papers/6a22672f763171746d545e6dhttps://doi.org/10.1007/s10517-026-06692-z
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