Delta-like ligand 4 mediated myeloid-derived suppressor cell metabolic reprogramming promotes neoadjuvant therapy

Yanfang Yang1,2, Ziyun Liu3, Parhat Kaysar3

  • 1Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin's Clinical Research Center for Cancer, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin, 300060, China.

Molecular Biomedicine
|December 1, 2025
PubMed

Insights

Titin (TTN) inactivation in triple-negative breast cancer (TNBC) promotes immune escape and drug resistance by enhancing myeloid-derived suppressor cell (MDSC) glycolysis via DLL4 signaling. Blocking this axis improves anti-tumor immunity and therapeutic response.

Area of Science:

  • Oncology
  • Immunology
  • Genetics

Background:

  • Triple-negative breast cancer (TNBC) presents a complex genomic landscape and significant treatment resistance.
  • Titin (TTN) inactivation, defined by TTN deficiency or mutation, impacts tumor progression, but its role in immune escape and therapeutic resistance is not fully understood.

Purpose of the Study:

  • To investigate the mechanisms by which TTN inactivation influences immune escape and therapeutic resistance in TNBC.
  • To explore the potential of targeting the TTN-DLL4-MDSC axis for novel immunotherapeutic strategies in TNBC.

Main Methods:

  • Whole-exome, single-cell, and spatial transcriptome sequencing were employed to analyze TNBC patients with TTN inactivation undergoing neoadjuvant therapy.
  • CRISPR-Cas9 technology was used to create mutant TNBC cell lines, and in vivo studies validated TTN and delta-like ligand 4 (DLL4) interactions.
  • Myeloid-derived suppressor cell (MDSC) metabolic function and the effects of DLL4 on TNBC were assessed in preclinical models.

Main Results:

  • TTN deficiency/mutation leads to DLL4 secretion in TNBC, which enhances MDSC glycolysis and lactate excretion via the NOTCH2 signaling pathway.
  • DLL4-induced MDSCs promote stemness-driven drug resistance in TNBC by altering histone lactate modification and suppressing CD8+ T cell activity.
  • Blocking the DLL4-MCT4 axis revitalized anti-tumor immunity and synergized with anti-PD-1 therapy, enhancing treatment response in a TNBC mouse model.

Conclusions:

  • TTN inactivation creates a pro-tumorigenic microenvironment in TNBC by modulating MDSC function through the DLL4-NOTCH2-MCT4 axis.
  • Targeting the DLL4-MCT4 pathway represents a promising strategy to overcome immune escape and enhance immunotherapy efficacy in TTN-inactivated TNBC.