CTHRC1 drives megakaryocyte-mediated immunotherapy resistance in esophageal squamous cell carcinoma via the integrin αIIbβ3/Rap1 pathway and is targetable by mRNA vaccination

Mol Cancer. 2026 May 21;25(1):178. doi: 10.1186/s12943-026-02670-1.

Abstract

The clinical efficacy of immunotherapy in advanced esophageal squamous cell carcinoma (ESCC) remains suboptimal, as most patients eventually develop drug resistance and experience disease progression. Here, we identify Collagen Triple Helix Repeat Containing 1 (CTHRC1) as a critical mediator of immunotherapy resistance in ESCC. Elevated CTHRC1 expression was observed in tumors unresponsive to immune checkpoint blockade and was associated with enhanced platelet activity and infiltration of megakaryocytes (MKs) into the tumor microenvironment. Mechanistically, CTHRC1 facilitated MK activation and recruitment, fostering an immunosuppressive niche that impaired cytotoxic T-cell activity and promoted cell exhaustion. To therapeutically target this axis, we developed a lipid nanoparticle (LNP)-encapsulated mRNA vaccine encoding CTHRC1. In preclinical ESCC models, the CTHRC1-mRNA-LNP vaccine elicited robust antitumor immunity. Notably, the combination of CTHRC1-mRNA vaccination with anti-PD-1 therapy induced synergistic intratumoral T-cell infiltration, depletion of MKs, reversal of immunosuppression, and durable tumor regression. Collectively, these findings uncover an unrecognized immunoregulatory function of CTHRC1 in ESCC and highlight its therapeutic targeting as a promising strategy to enhance the efficacy of immune checkpoint blockade.

Keywords: CTHRC1; Esophageal squamous cell carcinoma; Immunotherapy resistance; Megakaryocytes; mRNA vaccine.

MeSH terms

  • Animals
  • Cancer Vaccines* / immunology
  • Cell Line, Tumor
  • Drug Resistance, Neoplasm*
  • Esophageal Neoplasms* / genetics
  • Esophageal Neoplasms* / immunology
  • Esophageal Neoplasms* / metabolism
  • Esophageal Neoplasms* / pathology
  • Esophageal Neoplasms* / therapy
  • Esophageal Squamous Cell Carcinoma* / genetics
  • Esophageal Squamous Cell Carcinoma* / immunology
  • Esophageal Squamous Cell Carcinoma* / metabolism
  • Esophageal Squamous Cell Carcinoma* / pathology
  • Esophageal Squamous Cell Carcinoma* / therapy
  • Extracellular Matrix Proteins
  • Female
  • Humans
  • Immunotherapy* / methods
  • Mice
  • RNA, Messenger / genetics
  • Signal Transduction
  • Tumor Microenvironment / immunology
  • Xenograft Model Antitumor Assays
  • mRNA Vaccines* / administration & dosage
  • mRNA Vaccines* / immunology

Substances

  • CTHRC1 protein, human
  • Cancer Vaccines
  • mRNA Vaccines
  • RNA, Messenger
  • Extracellular Matrix Proteins