Inhibiting S-palmitoylation arrests metastasis by relocating Rap2b from plasma membrane in colorectal cancer

Rap2b, a proto-oncogene upregulated in colorectal cancer (CRC), undergoes protein S-palmitoylation at specific C-terminus sites (C176/C177). These palmitoylation sites are crucial for Rap2b localization on the plasma membrane (PM), as mutation of C176 or C177 results in cytosolic relocation of Rap2b. Our study demonstrates that Rap2b influences cell migration and invasion in CRC cells, independent of proliferation, and this activity relies on its palmitoylation. We identify ABHD17a as the depalmitoylating enzyme for Rap2b, altering PM localization and inhibiting cell migration and invasion. EGFR/PI3K signaling regulates Rap2b palmitoylation, with PI3K phosphorylating ABHD17a to modulate its activity. These findings highlight the potential of targeting Rap2b palmitoylation as an intervention strategy. Blocking the C176/C177 sites using an interacting peptide attenuates Rap2b palmitoylation, disrupting PM localization, and suppressing CRC metastasis. This study offers insights into therapeutic approaches targeting Rap2b palmitoylation for the treatment of metastatic CRC, presenting opportunities to improve patient outcomes.

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Publication Details

Journal
Cell Death and Disease
Published
2024-09-14
DOI
https://doi.org/10.1038/s41419-024-07061-2
Citations
11
Primary Topic
Cancer, Lipids, and Metabolism
Type
article
Field-Weighted Citation Impact
3.14

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article

Inhibiting S-palmitoylation arrests metastasis by relocating Rap2b from plasma membrane in colorectal cancer

Zhenshuai Chen, Yinming Liang, Jinghang Zhang, Yu Song et al.
11 citations
Cell Death and Disease
Cancer, Lipids, and Metabolism
3.14
article

Inhibiting S-palmitoylation arrests metastasis by relocating Rap2b from plasma membrane in colorectal cancer

Zhenshuai Chen, Yinming Liang, Jinghang Zhang, Yu Song, Binhui Zhou, Lingling Xi, Shiqian Qi, Sheng Jiang, Xize Cao, Jiangli Zhu, Eryan Kong, Tianyu Wang, Fei Cao, Shaohui Zhu, Birou Lai, Xiaohong Kang
article en
11 citations

Abstract

Rap2b, a proto-oncogene upregulated in colorectal cancer (CRC), undergoes protein S-palmitoylation at specific C-terminus sites (C176/C177). These palmitoylation sites are crucial for Rap2b localization on the plasma membrane (PM), as mutation of C176 or C177 results in cytosolic relocation of Rap2b. Our study demonstrates that Rap2b influences cell migration and invasion in CRC cells, independent of proliferation, and this activity relies on its palmitoylation. We identify ABHD17a as the depalmitoylating enzyme for Rap2b, altering PM localization and inhibiting cell migration and invasion. EGFR/PI3K signaling regulates Rap2b palmitoylation, with PI3K phosphorylating ABHD17a to modulate its activity. These findings highlight the potential of targeting Rap2b palmitoylation as an intervention strategy. Blocking the C176/C177 sites using an interacting peptide attenuates Rap2b palmitoylation, disrupting PM localization, and suppressing CRC metastasis. This study offers insights into therapeutic approaches targeting Rap2b palmitoylation for the treatment of metastatic CRC, presenting opportunities to improve patient outcomes.

Cell Death and DiseaseVol. 15(9)
China Pharmaceutical University (CN), Sichuan University (CN), Lanka Hospitals (LK), First Affiliated Hospital of Xinxiang Medical University (CN), State Key Laboratory of Biotherapy, Henan Medical University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Henan Province
Good health and well-being
Openalex Percentile: Top 7%
Cancer, Lipids, and Metabolism
3.14
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