CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Therapeutic Potential of Ginger Rhizomes (Zingiber officinale) on Leukemia.
Therapeutic Potential of Ginger Rhizomes (Zingiber officinale) on Leukemia.
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白血病由于复发、耐药和治疗相关毒性,持续构成重大的治疗挑战,这些问题常常阻碍疾病的持续管理。生姜(Zingiber officinale)的根茎含有生物活性酚类物质,尤其是6-姜酚和6-姜烯酚衍生物,这些物质在临床前模型中已显示出抗白血病疗效。
本研究严格评估了生姜来源制剂和分离化合物在急性和慢性白血病模型中的证据,重点关注反复出现的机制和转化可行性。在白血病细胞系研究和少量耐药模型数据中,生姜相关干预始终与活力降低和线粒体凋亡诱导相关,通常表现为Bax/Bcl-2比值改变、PARP断裂和caspase相关指标的变化。大量研究表明氧化还原调节,通常以白血病细胞内活性氧升高为特征,同时伴有促生存信号减弱,如PI3K/Akt,表现为pAkt和survivin水平降低。所提出的免疫调节和抗炎作用,包括NK细胞活性以及TNF-和IL-6等细胞因子的改变,在白血病特异性免疫背景中证据不足。由于提取物组成和化学表征的变异性、剂量和暴露条件不一致、依赖终点标志物而缺乏因果性操作,以及缺乏白血病特异性临床数据,解释受到限制。姜来源化合物具有多靶点生物活性,需要通过标准化和化学定义明确的制剂、药代动力学和药效学表征、临床相关暴露基准,以及精心设计的以白血病为重点的转化研究和早期临床研究,来进一步探索其安全性、有效性以及与当前疗法的相容性。
Leukemia continues to provide a significant therapeutic challenge due to relapse, medication resistance, and treatment-associated toxicity, which frequently hinder sustained disease management. Rhizomes of ginger (Zingiber officinale) possess bioactive phenolics, notably 6-gingerol and 6-shogaol derivatives, which have demonstrated antileukemia efficacy in preclinical models.
This study rigorously assesses the evidence regarding ginger-derived preparations and isolated compounds in both acute and chronic leukemia models, focusing on recurring mechanisms and translational viability. In leukemia cell line investigations and sparse resistant-model data, ginger-related interventions are consistently linked to diminished viability and the induction of mitochondrial apoptosis, typically indicated by alterations in Bax/Bcl-2 ratios, PARP breakage, and caspase-related measurements. Numerous studies indicate redox modulation, often characterized by elevated intracellular reactive oxygen species in leukemic cells, coupled with diminished pro-survival signaling, such as PI3K/Akt, as indicated by decreased pAkt and survivin levels.
The suggested immunomodulatory and anti-inflammatory effects, encompassing alterations in NK-cell activity and cytokines like TNF- and IL-6, are inadequately substantiated within leukemia-specific immunological contexts. Interpretation is limited by the variability in extract composition and chemical characterisation, inconsistent dose and exposure circumstances, dependence on endpoint markers without causative manipulation, and a lack of leukemia-specific clinical data.
Ginger-derived compounds exhibit multi-target biological activity that necessitates further exploration through standardized and chemically defined preparations, pharmacokinetic and pharmacodynamic characterization, clinically relevant exposure benchmarks, and meticulously designed leukemia-focused translational and early-phase clinical studies to elucidate safety, efficacy, and compatibility with current therapies.
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