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乳腺癌中的缺氧诱导因子:预后指标与新兴生物标志物:叙述性综述

Hypoxia-inducible factors in breast cancer: prognostic indicators and emerging biomarkers: narrative review.

作者信息

Obeagu Emmanuel Ifeanyi

机构信息

Department of Biomedical and Laboratory Science, Africa University, Mutare, Zimbabwe.

出版信息

Ann Med Surg (Lond). 2025 Jun 16;87(9):5614-5623. doi: 10.1097/MS9.0000000000003500. eCollection 2025 Sep.

Abstract

The hypoxia-inducible factor (HIF) pathway is a critical regulator of cellular responses to low oxygen conditions, which are prevalent in solid tumors like breast cancer. Under hypoxic conditions, HIF transcription factors, particularly HIF-1α and HIF-2α, orchestrate various tumor-promoting processes, including angiogenesis, metabolic reprogramming, and metastasis. These adaptive responses contribute significantly to tumor progression and resistance to conventional therapies. As such, understanding the molecular mechanisms underlying the HIF pathway offers valuable insights into breast cancer biology and provides a foundation for the development of novel therapeutic strategies. Recent advancements in the identification of biomarkers associated with the HIF pathway have shown potential for improving prognosis and guiding therapeutic decisions. Biomarkers such as HIF-1α, vascular endothelial growth factor, glucose transporter 1, and carbonic anhydrase IX are linked to hypoxia-driven tumor behaviors and may serve as indicators of disease aggressiveness and patient outcomes. Their integration into clinical practice could enable more precise stratification of patients for HIF-targeted interventions, facilitating the move toward personalized treatment regimens in breast cancer care.

摘要

缺氧诱导因子(HIF)通路是细胞对低氧条件反应的关键调节因子,低氧条件在乳腺癌等实体瘤中普遍存在。在缺氧条件下,HIF转录因子,特别是HIF-1α和HIF-2α,协调各种促进肿瘤的过程,包括血管生成、代谢重编程和转移。这些适应性反应对肿瘤进展和对传统疗法的抗性有显著贡献。因此,了解HIF通路的分子机制为乳腺癌生物学提供了有价值的见解,并为开发新的治疗策略奠定了基础。最近在鉴定与HIF通路相关的生物标志物方面的进展显示出改善预后和指导治疗决策的潜力。诸如HIF-1α、血管内皮生长因子、葡萄糖转运蛋白1和碳酸酐酶IX等生物标志物与缺氧驱动的肿瘤行为相关,可能作为疾病侵袭性和患者预后的指标。将它们整合到临床实践中可以使患者更精确地分层以进行HIF靶向干预,促进乳腺癌护理向个性化治疗方案的转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9b0/12401355/69aa0f6c4185/ms9-87-5614-g001.jpg

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