# Separase Inhibition Enhances Gefitinib Sensitivity of Lung Cancer via PTBP1/TAK1/RIPK1‐Mediated PANoptosis

**Authors:** Zhouyangfan Peng, Liangpeng Xie, Sufang Zhou, Yapei Li

PMC · DOI: 10.1002/mco2.70432 · MedComm · 2025-10-20

## TL;DR

Inhibiting separase with Sepin-1 improves gefitinib's effectiveness in lung cancer by triggering PANoptosis, a form of cell death.

## Contribution

A new strategy for overcoming gefitinib resistance in lung cancer via separase inhibition and PANoptosis induction.

## Key findings

- Sepin-1 enhances gefitinib-induced cytotoxicity in lung cancer cells through PANoptosis.
- Combining Sepin-1 and gefitinib significantly reduces lung xenograft tumor growth in vivo.
- Lower separase expression or higher PANoptosis markers correlate with better gefitinib response in patients.

## Abstract

Gefitinib is the most frequently employed anti‐lung cancer drug, but its clinical effectiveness is often compromised due to the development of drug resistance. Given that gefitinib failure to long‐term inhibition of the growth of lung carcinoma cell lines, which mirrors the resistance observed in clinical patients, new approaches to improve the curative effect of gefitinib should be found. Surprisedly, inhibiting separase with the specific inhibitor Sepin‐1 has been found to effectively enhance gefitinib‐induced cytotoxic in lung cancer cell by promoting the development of PANoptosis, which includes pyroptosis, apoptosis, and necroptosis. Moreover, in vivo experiments also demonstrated that the combination of Sepin‐1 and gefitinib can induce significant regression of lung xenograft tissues. Mechanically, loss of separase plus gefitinib decreases the expression of PTBP1 and TAK1. Overexpression of PTBP1 or TAK1 suppresses this interaction‐induced PANoptosis by promoting the inactivation of RIPK1. In addition, clinical data showed that better effective of gefitinib maybe associated with lower separase expression or higher PANoptosis marker expression in patient lung carcinoma tissues. Thus, these findings provide a novel anti‐lung cancer strategy and highlight separase as a potential target for overcoming gefitinib resistance in lung cancer treatment.

Inhibiting separase with the specific inhibitor Sepin‐1 has been found to effectively enhance gefitinib‐induced cytotoxic in lung cancer cell. Mechanically, separase inhibitor Sepin‐1 plus gefitinib decreases the expression of PTBP1 and TAK1 to trigger RIPK1‐dependent PANoptosis.

## Linked entities

- **Genes:** ESP (separase) [NCBI Gene 828396], PTBP1 (polypyrimidine tract binding protein 1) [NCBI Gene 5725], MAP3K7 (mitogen-activated protein kinase kinase kinase 7) [NCBI Gene 6885], RIPK1 (receptor interacting serine/threonine kinase 1) [NCBI Gene 8737]
- **Chemicals:** Gefitinib (PubChem CID 123631), Sepin-1 (PubChem CID 2736269)
- **Diseases:** lung cancer (MONDO:0005138)

## Full-text entities

- **Genes:** ESPL1 (extra spindle pole bodies like 1, separase) [NCBI Gene 9700] {aka ESP1, SEPA}, PTBP1 (polypyrimidine tract binding protein 1) [NCBI Gene 5725] {aka HNRNP-I, HNRNPI, HNRPI, PTB, PTB-1, PTB-T}, RIPK1 (receptor interacting serine/threonine kinase 1) [NCBI Gene 8737] {aka AIEFL, IMD57, RIP, RIP-1, RIP1}, MAP3K7 (mitogen-activated protein kinase kinase kinase 7) [NCBI Gene 6885] {aka CSCF, FMD2, MEKK7, TAK1, TGF1a}
- **Diseases:** Lung Cancer (MESH:D008175), cytotoxic (MESH:D064420)
- **Chemicals:** Gefitinib (MESH:D000077156), Sepin-1 (MESH:C000710218)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12536889/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12536889/full.md

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Source: https://tomesphere.com/paper/PMC12536889