본문으로 건너뛰기
← 뒤로

ERO1α as a Potential Drug Target for Breast Cancer: A Systematic Review of Current Evidence.

메타분석 1/5 보강
International journal of molecular sciences 📖 저널 OA 100% 2021: 8/8 OA 2022: 38/38 OA 2023: 49/49 OA 2024: 103/103 OA 2025: 453/453 OA 2026: 454/454 OA 2021~2026 2025 Vol.26(21)
Retraction 확인
출처

Khojayeva K, Moldasheva A, Aljofan M

📝 환자 설명용 한 줄

Hypoxia, oxidative stress, and impaired protein folding contribute to tumor progression and therapy resistance.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 연구 설계 systematic review

이 논문을 인용하기

↓ .bib ↓ .ris
APA Khojayeva K, Moldasheva A, Aljofan M (2025). ERO1α as a Potential Drug Target for Breast Cancer: A Systematic Review of Current Evidence.. International journal of molecular sciences, 26(21). https://doi.org/10.3390/ijms262110276
MLA Khojayeva K, et al.. "ERO1α as a Potential Drug Target for Breast Cancer: A Systematic Review of Current Evidence.." International journal of molecular sciences, vol. 26, no. 21, 2025.
PMID 41226317 ↗

Abstract

Hypoxia, oxidative stress, and impaired protein folding contribute to tumor progression and therapy resistance. Endoplasmic Reticulum Oxidoreductin 1 Alpha (ERO1α) is a key enzyme regulating redox homeostasis in the endoplasmic reticulum by reoxidizing protein disulfide isomerase, facilitating disulfide bond formation, and generating reactive oxygen species. Elevated ERO1α levels are associated with increased tumor aggressiveness, metastasis, and poor clinical outcomes. Despite growing evidence of its tumor-promoting functions, no clinically approved ERO1α inhibitors exist. This systematic review provides a comprehensive and integrative analysis of current research on ERO1α in breast cancer, emphasizing its roles in hypoxia response, angiogenesis, immune modulation, and ferroptosis resistance. We discuss mechanistic links, including VEGF-A maturation and PD-L1-mediated immune evasion, and highlight recent advances in small-molecule ERO1α inhibitors and preclinical therapeutic strategies. By consolidating molecular insights and translational considerations, this review underscores ERO1α as both a promising therapeutic target and potential prognostic marker, offering guidance for future drug development and targeted interventions in redox-dependent cancer pathways.

🏷️ 키워드 / MeSH 📖 같은 키워드 OA만

🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반

🟢 PMC 전문 열기