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June 1, 2026ACS Applied Materials & Interfaces0 citations

A Phosphoproteomic Platform Identifies Erythrocyte Membrane Protein Band 4.1-Like 3-Mediated Lipid Droplet Remodeling Linked to Liver Cancer Invasion and Migration

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JMJianwen MaoYXYan XiaXLXue-Yang Luo

Key Points

  • The research aims to unravel the regulatory mechanisms of lipid droplet dynamics in hepatocellular carcinoma and their impact on tumor progression.
  • Developed an ultrasensitive phosphoproteomic platform to analyze LD-associated phosphorylation events across six HCC cell lines.
  • Conducted functional perturbation screens to assess the roles of various phosphoproteins in LD size regulation.
  • Identified key phosphorylation sites on EPB41L3 that affect its regulatory function and HCC metastatic potential.
  • Silencing specific phosphoproteins (SH3KBP1, SLK, EHD2, EPB41L3, NEXN) reduced LD size in Huh1 cells, while others (CPD, BET1, UFL1, RRP1B, OGFR, CD2BP2) enlarged LDs in Huh7 cells.
  • Loss of EPB41L3 decreased LD size and accelerated migration and invasion of HCC cells, associated with poor clinical outcomes.
  • Five essential phosphorylation sites on EPB41L3 were identified; mutations abolished its regulatory effects on LD size and HCC metastasis.

Abstract

Aberrant lipid metabolism is a hallmark of hepatocellular carcinoma (HCC), yet the regulatory mechanisms governing lipid droplet (LD) dynamics and their contribution to tumor progression remain poorly understood. Here, we developed an ultrasensitive phosphoproteomic platform using high-affinity HPDA@Ti4+ nanospheres to map LD-associated phosphorylation events across six HCC cell lines. By correlating phosphoproteomic signatures with LD morphology, we identified distinct regulatory signatures associated with LD size and abundance. Functional perturbation screens identified two distinct phosphoprotein modules controlling LD size: silencing SH3KBP1, SLK, EHD2, EPB41L3, and NEXN reduced LD size in Huh1 cells, whereas silencing CPD, BET1, UFL1, RRP1B, OGFR, and CD2BP2 enlarged LDs in Huh7 cells. Notably, we identified EPB41L3 as a critical metabolic-metastatic link; its loss decreased LD size and accelerated HCC migration and invasion, correlating with poor clinical prognosis. Crucially, we identified five key phosphorylation sites on EPB41L3 essential for its function; substituting these with alanine completely abolished its regulatory control over both LD size and HCC metastatic potential. Together, these findings delineate a phosphorylation-based regulatory network controlling the LD architecture and metastatic potential in HCC. Our study not only identifies potential therapeutic targets but also establishes a generalizable phosphoproteomic framework for interrogating lipid signaling in cancer metabolism.

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Cite This Study

Mao et al. (2026) studied this question.

synapsesocial.com/papers/6a1d218f02fbce9130637973https://doi.org/10.1021/acsami.6c02180
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