Organoplatinum(II) Type II Immunogenic Cell Death Inducers Target Protein Tyrosine Phosphatase 1B to Drive

Jiao Xia Zou1, Pavel A Ivanov-Rostovtsev2, Jemma Arakelyan2

  • 1Department of Chemistry, National University of Singapore, 4 Science Drive 2, Singapore 117543, Singapore.

Insights

Researchers identified Protein Tyrosine Phosphatase 1B (PTP1B) as a key target for immunogenic cell death (ICD) inducers like Pt-ER and Pt-NHC. Inhibiting PTP1B enhances cancer cell immunogenicity, offering new avenues for chemoimmunotherapy.

Area of Science:

  • Biochemistry
  • Molecular Biology
  • Cancer Research

Background:

  • Immunogenic cell death (ICD) inducers are crucial chemotherapeutics for anti-tumor immunity.
  • Molecular targets of ICD inducers are not fully understood, limiting therapeutic development.

Purpose of the Study:

  • To identify direct molecular targets of ICD inducers.
  • To investigate the role of these targets in ICD and colorectal cancer.

Main Methods:

  • Validation of Pt-NHC and Pt-ER as ICD inducers.
  • Design of photoactivable probes based on Pt-ER.
  • Quantitative proteomics and biochemical assays to identify PTP1B as a target.
  • Genetic knockdown and pharmacological inhibition of PTP1B.
  • Bioinformatic analysis of PTP1B in colorectal cancer.

Main Results:

  • Pt-ER and Pt-NHC were confirmed as ICD inducers, establishing immunity against colorectal cancer.
  • PTP1B was identified as a direct target of Pt-ER, crucial for ICD.
  • Both Pt-ER and Pt-NHC directly inhibit PTP1B enzymatic activity.
  • PTP1B suppression increased tumor cell surface calreticulin and phagocytosis, enhancing immunogenicity.
  • PTP1B was implicated in colorectal cancer progression and immune regulation.

Conclusions:

  • This study reveals PTP1B as a novel modulator of ICD.
  • PTP1B inhibition enhances cancer cell immunogenicity, suggesting therapeutic potential in chemoimmunotherapy.

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