PICK1 modulates the proliferation and migration of gastric cancer cells by regulating TLR4

Protein interacting with C kinase 1 (PICK1) interacts with a variety of membrane proteins and receptors involved in nervous system diseases and multiple cancers. However, the role of PICK1 in gastric cancer remains unclear. In the present work, we explored the expression and interactions of PICK1 with Toll-like receptor 4 (TLR4) in gastric cancer. Clinical data analysis showed that PICK1 expression decreases and is predictive of worse outcomes in patients with gastric cancer. High PICK1 levels attenuate the proliferation and migration of gastric cancer cells, which is dependent on the TLR4/myeloid differentiation primary response 88 (MyD88) signaling pathway. Furthermore, in vitro experiments demonstrated that PICK1 affects the trafficking and degradation of TLR4 and promotes TLR4 degradation via autophagy in gastric cancer cells. Molecular dynamics simulations highlighted the binding strength and stability of the TLR4-PICK1 complex. Our study provides new insights into the cellular and pathological functions of PICK1 in gastric cancer.

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Journal
Journal of Zhejiang University SCIENCE B
Published
2025-11-29
DOI
https://doi.org/10.1631/jzus.b2400167
Primary Topic
Immune Response and Inflammation
Type
article
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article

PICK1 modulates the proliferation and migration of gastric cancer cells by regulating TLR4

Bingyu Chen, Xiao‐San Luo, Qianni Wang, Kaiqiang Li et al.
Journal of Zhejiang University SCIENCE B
Immune Response and Inflammation
article

PICK1 modulates the proliferation and migration of gastric cancer cells by regulating TLR4

Bingyu Chen, Xiao‐San Luo, Qianni Wang, Kaiqiang Li, Jingling Jin, Lina Peng, Zhen Wang, Yaling Wang, Peng Xu, Aibo Xu, Ke Hao, Yimin Yang, Wei Yang
article en

Abstract

Protein interacting with C kinase 1 (PICK1) interacts with a variety of membrane proteins and receptors involved in nervous system diseases and multiple cancers. However, the role of PICK1 in gastric cancer remains unclear. In the present work, we explored the expression and interactions of PICK1 with Toll-like receptor 4 (TLR4) in gastric cancer. Clinical data analysis showed that PICK1 expression decreases and is predictive of worse outcomes in patients with gastric cancer. High PICK1 levels attenuate the proliferation and migration of gastric cancer cells, which is dependent on the TLR4/myeloid differentiation primary response 88 (MyD88) signaling pathway. Furthermore, in vitro experiments demonstrated that PICK1 affects the trafficking and degradation of TLR4 and promotes TLR4 degradation via autophagy in gastric cancer cells. Molecular dynamics simulations highlighted the binding strength and stability of the TLR4-PICK1 complex. Our study provides new insights into the cellular and pathological functions of PICK1 in gastric cancer.

Journal of Zhejiang University SCIENCE BVol. 27(1)
Blood Center of Zhejiang Province (CN), The Third Affiliated Hospital of Zhejiang Chinese Medical University (CN), Hangzhou Medical College (CN), First Affiliated Hospital Zhejiang University (CN), Zhejiang University of Technology (CN)
Openalex Percentile: Top 58%
Immune Response and Inflammation
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