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氯沙坦在肿瘤治疗中的研究现状

英文原题:Current Status of Research on Losartan in Tumour Therapy.

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Current Status of Research on Losartan in Tumour Therapy.

PubMed 2026/01/01(内容时间) J Cell Mol Med Q2 · IF 4.7(JCR 2025)

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中文摘要

氯沙坦是一种广泛使用的降压药,因价格低廉、安全性已有充分认识且作用多效,作为癌症治疗辅助药物日益受到关注。新兴临床前证据显示,氯沙坦可通过抑制转化生长因子β(TGF-β)信号、降低基质硬度并改善血管灌注,有效调节肿瘤微环境(TME)。这些变化可增强化疗药物递送和疗效;若与纳米载体联用,通过增强高通透性和滞留效应,作用可能进一步放大。除重塑TME外,氯沙坦在胰腺癌、乳腺癌和结直肠癌等多种临床前模型中还表现出抗肿瘤活性。

机制上,阻断血管紧张素II 1型受体(AT1R)可调节PI3K/AKT和YAP/TAZ等关键致癌通路,并可能通过下调VEGF等机制促进血管正常化,缓解缺氧并改善放疗应答。证据还提示氯沙坦可通过促进CD8⁺ T细胞和自然杀伤(NK)细胞浸润、重编程肿瘤相关巨噬细胞(TAM)以及抑制免疫抑制性细胞因子,重塑肿瘤免疫环境。

此外,氯沙坦似乎还能抑制上皮—间质转化(EMT)及CXCR4/SDF-1、基质金属蛋白酶(MMP)等转移相关通路。这些多方面机制凸显其作为治疗辅助药物的潜力,可突破基质屏障、减轻免疫逃逸并限制转移播散。

然而,将令人鼓舞的临床前发现转化为临床实践仍是一大挑战。不同癌种中的疗效不一、临床证据尚处早期,以及最佳患者选择和剂量等未决问题,均使前景仍需审慎看待。目前临床验证主要限于早期试验;最佳剂量、治疗顺序及肿瘤患者长期安全性等关键参数仍待严格界定。本综述综合氯沙坦用于实体瘤的机制与转化研究,旨在阐明其抗癌特性、探讨其与纳米及免疫治疗的协同作用、批判性评估相关挑战,并确定临床应用的关键证据缺口和未来方向。临床试验注册号:NCT01821729和NCT03563248。

展开英文摘要原文

Losartan, a widely prescribed antihypertensive agent, has attracted growing interest as a potential adjuvant in cancer therapy due to its affordability, established safety profile and pleiotropic effects. Emerging preclinical evidence demonstrates that losartan can effectively modulate the tumour microenvironment (TME) by inhibiting transforming growth factor- (TGF- ) signalling, reducing stromal stiffness and improving vascular perfusion.

These changes are shown to enhance the delivery and efficacy of chemotherapeutic agents, an effect potentially amplified when combined with nanocarriers by augmenting the enhanced permeability and retention effect. Beyond TME remodelling, losartan has demonstrated anti-tumour activity across various preclinical models, including those of pancreatic, breast and colorectal cancers.

Mechanistically, angiotensin II type 1 receptor (AT1R) blockade is reported to modulate key downstream oncogenic pathways, including PI3K/AKT and YAP/TAZ, and to promote vascular normalisation via mechanisms that may include VEGF downregulation, thereby alleviating hypoxia and improving radiotherapy response.

Furthermore, evidence suggests losartan remodels the tumour immune landscape by promoting CD8 + T and natural killer (NK) cell infiltration, reprogramming tumour-associated macrophages (TAMs) and suppressing immunosuppressive cytokines.

It also appears to inhibit epithelial-mesenchymal transition (EMT) and metastasis-related pathways, including CXCR4/SDF-1 and matrix metalloproteinases (MMPs). These multifaceted mechanisms highlight its potential as a therapeutic adjuvant capable of overcoming stromal barriers, mitigating immune evasion and limiting metastatic dissemination.

However, the translation of these compelling preclinical findings into clinical practice remains a major challenge. The promising preclinical data are tempered by variable efficacy across cancer types, a nascent clinical evidence base and unresolved questions regarding optimal patient selection and dosing. Clinical validation is still nascent, predominantly limited to early-phase trials and critical parameters such as optimal dosing, treatment sequencing and long-term safety in oncology patients await rigorous definition.

This review synthesises the current mechanistic and translational research on losartan in solid tumours, aiming to clarify its anti-cancer properties, explore its synergy with nano- and immune-therapeutics, critically assess the associated challenges and identify key gaps and future directions for clinical application. Trial Registration: ClinicalTrials. gov identifier: NCT01821729 and NCT03563248.

论文信息

作者
Wang H、Yuan S、Wang H
单位
Department of Obstetrics and Gynecology, Key Laboratory of Birth Defects and Related Diseases of Women and Children of the Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, China.China
文献类型
综述
期刊
Journal of cellular and molecular medicine2026 Jan
原文标识
PubMed 41486497 · DOI 10.1111/jcmm.70985