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Blu-Ray-Based Quantification of CD98+ Extracellular Vesicles for Early Detection of Hepatocellular Carcinoma.

1/5 보강
Cancers 2026 Vol.18(7)
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
환자: early-stage (stage I/II) non-viral HCC ( = 136) and healthy controls ( = 50), CD98+ EV levels were significantly elevated ( < 0
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Importantly, CD98+ EV levels detected small tumors (≤3 cm) with 59% sensitivity, outperforming AFP (33%). These findings highlight circulating CD98+ EVs as a promising, noninvasive biomarker for early non-viral HCC detection, providing a clinically applicable platform that integrates EV quantification with a novel anti-CD98 monoclonal antibody for precision oncology.

Chen SL, Low YS, Huang BR, Lu CH, Lan WC, Wu RH, Lin HY, Yueh A, Hsu EC

📝 환자 설명용 한 줄

Hepatocellular carcinoma (HCC) remains a major global health burden, with an increasing incidence driven by metabolic syndrome-related cases.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • Sensitivity 64%
  • Specificity 86%

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BibTeX ↓ RIS ↓
APA Chen SL, Low YS, et al. (2026). Blu-Ray-Based Quantification of CD98+ Extracellular Vesicles for Early Detection of Hepatocellular Carcinoma.. Cancers, 18(7). https://doi.org/10.3390/cancers18071086
MLA Chen SL, et al.. "Blu-Ray-Based Quantification of CD98+ Extracellular Vesicles for Early Detection of Hepatocellular Carcinoma.." Cancers, vol. 18, no. 7, 2026.
PMID 41976309

Abstract

Hepatocellular carcinoma (HCC) remains a major global health burden, with an increasing incidence driven by metabolic syndrome-related cases. Early detection is critical; however, current diagnostic tools, including ultrasonography and alpha-fetoprotein (AFP), lack adequate sensitivity and specificity, particularly for non-viral HCC. In this "discovery-stage" study, we identified CD98, a transmembrane oncoprotein, as a robust biomarker highly expressed across all HCC stages, independent of etiological factors. CD98 is enriched on extracellular vesicles (EVs) released by HCC cells and can be accurately quantified using Blu-ray-based ExoCounter technology. In plasma samples from patients with early-stage (stage I/II) non-viral HCC ( = 136) and healthy controls ( = 50), CD98+ EV levels were significantly elevated ( < 0.001) and demonstrated strong diagnostic performance (AUC = 0.743; sensitivity 64%, specificity 86%). Importantly, CD98+ EV levels detected small tumors (≤3 cm) with 59% sensitivity, outperforming AFP (33%). These findings highlight circulating CD98+ EVs as a promising, noninvasive biomarker for early non-viral HCC detection, providing a clinically applicable platform that integrates EV quantification with a novel anti-CD98 monoclonal antibody for precision oncology.

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