CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Blood transfusion mediated tumor microenvironment remodeling in breast cancer.
Blood transfusion mediated tumor microenvironment remodeling in breast cancer.
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输血在乳腺癌管理中起着关键作用,尤其是在处理围手术期失血和化疗引起的贫血方面。然而,新出现的证据表明,输血可能通过诱导输血相关免疫调节(TRIM)和改变肿瘤微环境(TME)而对肿瘤学结局产生不利影响。TRIM抑制细胞毒性免疫反应,可能促进肿瘤进展——尤其是在三阴性乳腺癌(TNBC)和HER2阳性癌症等侵袭性亚型中。
此外,输血可通过增加血液黏度和损害微血管灌注而矛盾性地加重肿瘤缺氧,从而降低化疗、放疗和免疫治疗的效果。本综述探讨了输血在乳腺癌中的双重作用,既强调其临床获益,也强调其潜在风险。
我们分析了输血对治疗耐药和肿瘤进展的影响,并讨论了减轻相关风险的策略,包括白细胞去除、促红细胞生成素刺激剂(ESAs)、静脉补铁和血液保护技术。
此外,我们强调了由肿瘤亚型、免疫状态以及相关生物标志物如TIL(肿瘤浸润淋巴细胞)(TILs)、PD-L1表达和循环肿瘤DNA(ctDNA)指导的个体化输血方法的重要性。未来研究应侧重于优化输血时机、实施生物标志物驱动的方案,以及开发免疫调节干预措施以对抗TRIM。个体化、基于证据的输血策略可能最终提高治疗效果并改善乳腺癌治疗的长期结局。
Blood transfusions play a critical role in breast cancer management, particularly in addressing perioperative blood loss and chemotherapy-induced anemia.
However, emerging evidence suggests that transfusions may adversely affect oncologic outcomes by inducing transfusion-related immunomodulation (TRIM) and altering the tumor microenvironment (TME). TRIM suppresses cytotoxic immune responses, potentially facilitating tumor progression-especially in aggressive subtypes such as triple-negative breast cancer (TNBC) and HER2-positive cancers.
Additionally, transfusions can paradoxically exacerbate tumor hypoxia by increasing blood viscosity and impairing microvascular perfusion, thereby reducing the effectiveness of chemotherapy, radiotherapy, and immunotherapy. This review examines the dual role of blood transfusions in breast cancer, emphasizing both their clinical benefits and potential risks.
We analyze their impact on treatment resistance and tumor progression and discuss strategies to mitigate associated risks, including leukoreduction, erythropoiesis-stimulating agents (ESAs), intravenous iron supplementation, and blood conservation techniques.
Furthermore, we highlight the importance of personalized transfusion approaches guided by tumor subtype, immune status, and relevant biomarkers such as tumor-infiltrating lymphocytes (TILs), PD-L1 expression, and circulating tumor DNA (ctDNA).
Future research should focus on optimizing transfusion timing, implementing biomarker-driven protocols, and developing immune-modulating interventions to counteract TRIM. A personalized, evidence-based transfusion strategy may ultimately enhance treatment efficacy and improve long-term outcomes in breast cancer care.
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