Data from <i>LINC00869</i> Promotes Hepatocellular Carcinoma Metastasis via Protrusion Formation
Данные о LINC00869 способствуют метастазированию гепатоцеллюлярной карциномы за счёт образования выступов
2024-03-01
SCID: 54.1/kgxx8sv2
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LINC00869WASP phosphorylation Y291WASP–CDC42 pathwayhepatocellular carcinomalong noncoding RNA
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Abstract (AI)
<div>Abstract<p>Coordination of filament assembly and membrane remodeling is required for the directional migration of cancer cells. The Wiskott–Aldrich syndrome protein (WASP) recruits the actin-related protein (ARP) 2/3 complex to assemble branched actin networks. The goal of our study was to assess the potential regulatory role exerted by the novel long noncoding RNA (lncRNA) <i>LINC00869</i> on hepatocellular carcinoma (HCC) cells. We used HCC cells to overexpress or knockdown <i>LINC00869</i>, analyzed patient data from publicly available databases and Cancer Hospital Affiliated with Zhengzhou University, and used a xenograft mouse model of HCC to study the molecular mechanism associated with <i>LINC00869</i> expression. We found that high levels of <i>LINC00869</i> expression were associated with poor prognosis in patients with HCC. Next, we detected an interaction between <i>LINC00869</i> and both WASP and ARP2 in HCC cells, and observed a modulatory effect of <i>LINC00869</i> on the phosphorylation of WASP at Y291 and the activity of cell division control protein 42 (CDC42). These modulatory roles were required for WASP/CDC42 activity on F-actin polymerization to enhance membrane protrusion formation and maintain persistent cell polarization. This, in turn, promoted the migration and invasion abilities of HCC cells. Finally, we confirmed the role of <i>LINC00869</i><i>in vivo</i>, using the tumor xenograft mouse model; and identified a positive correlation between <i>LINC00869</i> expression levels and the phosphorylation levels of WASP in HCC samples. Overall, our findings suggest a unique mechanism by which <i>LINC00869</i> orchestrates membrane protrusion during migration and invasion of HCC cells.</p>Implications:<p>LncRNA <i>LINC00869</i> regulates the activity of CDC42–WASP pathway and positively affects protrusion formation in HCC cells, which expands the current understanding of lncRNA functions as well as gives a better understanding of carcinogenesis.</p></div>
Key Findings
1
High LINC00869 expression in hepatocellular carcinoma (HCC) is associated with poor patient prognosis.
2
In vivo xenograft models confirm LINC00869 promotes tumor progression and correlate with increased WASP phosphorylation in HCC samples.
3
LINC00869 modulates WASP phosphorylation at Y291 and CDC42 activity, which are required for F-actin polymerization.
4
LINC00869 physically interacts with WASP and ARP2 in HCC cells.
5
LINC00869-driven regulation of the CDC42–WASP pathway enhances membrane protrusion formation, persistent cell polarization, and increases HCC cell migration and invasion.
Research Object
Long noncoding RNA LINC00869 in hepatocellular carcinoma cells
Research Subject
Regulation of CDC42–WASP/ARP2-mediated F-actin polymerization and membrane protrusion formation that promotes migration, invasion, and metastasis in HCC
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2024-03-01
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