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Src promotes tumor cell invasion by hijacking the translation machineries.

2/5 보강
Cell reports 📖 저널 OA 60.7% 2022: 1/1 OA 2024: 6/12 OA 2025: 20/55 OA 2026: 47/54 OA 2022~2026 2026 Vol.45(3) p. 116989 OA Cell Adhesion Molecules Research
TL;DR It is determined that Src regulates mRNA translation and controls the expression of eIF3 subunits, including eIF3h, eIF3e, and eIF3d, crucial for invadosome formation and ECM degradation.
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PubMed DOI OpenAlex Semantic 마지막 보강 2026-05-02

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
환자: hepatocellular carcinoma (HCC), promoting ECM degradation and tumor invasiveness of HCC cells
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Moreover, overexpression of Src and eIF3h/e/d correlates with poor prognosis in patients with hepatocellular carcinoma (HCC), promoting ECM degradation and tumor invasiveness of HCC cells. This study identifies Src as a major regulator of translation initiation, modulating invadosome formation, ECM degradation, and tumor cell invasion.
OpenAlex 토픽 · Cell Adhesion Molecules Research RNA and protein synthesis mechanisms Wnt/β-catenin signaling in development and cancer

Bonnard B, Chatefau A, Dourthe C, Di Tommaso S, Dupuy JW, Mahouche I

📝 환자 설명용 한 줄

It is determined that Src regulates mRNA translation and controls the expression of eIF3 subunits, including eIF3h, eIF3e, and eIF3d, crucial for invadosome formation and ECM degradation.

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APA B. Bonnard, Anouk Chatefau, et al. (2026). Src promotes tumor cell invasion by hijacking the translation machineries.. Cell reports, 45(3), 116989. https://doi.org/10.1016/j.celrep.2026.116989
MLA B. Bonnard, et al.. "Src promotes tumor cell invasion by hijacking the translation machineries.." Cell reports, vol. 45, no. 3, 2026, pp. 116989.
PMID 41734063 ↗

Abstract

The Src oncogene controls cancer cell invasiveness by promoting invadosome formation and extracellular matrix (ECM) degradation. Invadosomes are translational hotspots enriched in the eukaryotic translation initiation factor 3 (eIF3) complex that is mandatory for their maintenance. Here, we determined that Src regulates mRNA translation and controls the expression of eIF3 subunits, including eIF3h, eIF3e, and eIF3d. These subunits are crucial for invadosome formation and ECM degradation. Src also modulates both canonical eIF4E-dependent translation via the activation of the phosphoinositide-3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) pathway and the non-canonical translation mechanism through eIF3d overexpression, both of which are necessary for invadosome function. Moreover, overexpression of Src and eIF3h/e/d correlates with poor prognosis in patients with hepatocellular carcinoma (HCC), promoting ECM degradation and tumor invasiveness of HCC cells. This study identifies Src as a major regulator of translation initiation, modulating invadosome formation, ECM degradation, and tumor cell invasion.

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