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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.
Abstract:
Immunogenic cell death (ICD) inducers are valuable chemotherapeutic agents that elicit protective immune responses against tumors. Although many ICD inducers have emerged in recent years, specific molecular targets directly associated with ICD remain relatively unexplored. Here, two Type II ICD inducers, Pt-NHC and PlatinER (Pt-ER), were validated as bona fide ICD inducers with the ability to establish immunity against colorectal cancer in vivo. Based on Pt-ER, several ICD-inducing photoactivable probes were designed to capture their potential targets. By integrating quantitative proteomics analysis with biochemical assays, we identified PTP1B as a direct target of Pt-ER that engages in ICD. Both Pt-ER and Pt-NHC were shown to directly interact with PTP1B and inhibit its enzymatic activity. The suppression of PTP1B, by either genetic knockdown or pharmacological inhibition, enhanced the immunogenicity of tumor cells by increasing surface-exposed calreticulin and phagocytosis of cancer cells. Bioinformatic analysis also revealed that PTP1B plays a role in tumor progression and immune regulation in colorectal cancer. Therefore, our study first reveals a previously unrecognized role of PTP1B in modulating ICD and highlights its potential therapeutic values in cancer chemoimmunotherapy.
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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