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顺铂诱导的骨骼肌功能障碍:机制与治疗策略的对抗。

Cisplatin-Induced Skeletal Muscle Dysfunction: Mechanisms and Counteracting Therapeutic Strategies.

机构信息

Department of Pharmacy-Drug Sciences, University of Bari, 70125 Bari, Italy.

School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.

出版信息

Int J Mol Sci. 2020 Feb 13;21(4):1242. doi: 10.3390/ijms21041242.

Abstract

Among the severe side effects induced by cisplatin chemotherapy, muscle wasting is the most relevant one. This effect is a major cause for a clinical decline of cancer patients, since it is a negative predictor of treatment outcome and associated to increased mortality. However, despite its toxicity even at low doses, cisplatin remains the first-line therapy for several types of solid tumors. Thus, effective pharmacological treatments counteracting or minimizing cisplatin-induced muscle wasting are urgently needed. The dissection of the molecular pathways responsible for cisplatin-induced muscle dysfunction gives the possibility to identify novel promising therapeutic targets. In this context, the use of animal model of cisplatin-induced cachexia is very useful. Here, we report an update of the most relevant researches on the mechanisms underlying cisplatin-induced muscle wasting and on the most promising potential therapeutic options to preserve muscle mass and function.

摘要

在顺铂化疗引起的严重副作用中,肌肉减少症是最相关的一种。这种影响是癌症患者临床状况恶化的主要原因,因为它是治疗结果的负面预测因子,并与死亡率增加相关。然而,尽管其毒性即使在低剂量下,顺铂仍然是几种实体瘤的一线治疗药物。因此,迫切需要有效的药理学治疗方法来对抗或最小化顺铂引起的肌肉减少症。对导致顺铂诱导肌肉功能障碍的分子途径的剖析为确定新的有前途的治疗靶点提供了可能性。在这种情况下,使用顺铂诱导恶病质的动物模型非常有用。在这里,我们报告了关于顺铂诱导肌肉减少症的机制以及最有希望的潜在治疗方法的最新研究进展,以保持肌肉质量和功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/852d/7072891/154255ae098c/ijms-21-01242-g001.jpg

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