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化疗药物与线粒体功能障碍:以多柔比星、曲妥珠单抗和舒尼替尼为例。

Chemotherapeutic Drugs and Mitochondrial Dysfunction: Focus on Doxorubicin, Trastuzumab, and Sunitinib.

机构信息

Laboratory of Pathophysiology of Cachexia and Metabolism of Skeletal Muscle, IRCCS San Raffaele Pisana, 00166 Rome, Italy.

Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy.

出版信息

Oxid Med Cell Longev. 2018 Mar 18;2018:7582730. doi: 10.1155/2018/7582730. eCollection 2018.

Abstract

Many cancer therapies produce toxic side effects whose molecular mechanisms await full elucidation. The most feared and studied side effect of chemotherapeutic drugs is cardiotoxicity. Also, skeletal muscle physiology impairment has been recorded after many chemotherapeutical treatments. However, only doxorubicin has been extensively studied for its side effects on skeletal muscle. Chemotherapeutic-induced adverse side effects are, in many cases, mediated by mitochondrial damage. In particular, trastuzumab and sunitinib toxicity is mainly associated with mitochondria impairment and is mostly reversible. Vice versa, doxorubicin-induced toxicity not only includes mitochondria damage but can also lead to a more robust and extensive cell injury which is often irreversible and lethal. Drugs interfering with mitochondrial functionality determine the depletion of ATP reservoirs and lead to subsequent reversible contractile dysfunction. Mitochondrial damage includes the impairment of the respiratory chain and the loss of mitochondrial membrane potential with subsequent disruption of cellular energetic. In a context of increased stress, AMPK has a key role in maintaining energy homeostasis, and inhibition of the AMPK pathway is one of the proposed mechanisms possibly mediating mitochondrial toxicity due to chemotherapeutics. Therapies targeting and protecting cell metabolism and energy management might be useful tools in protecting muscular tissues against the toxicity induced by chemotherapeutic drugs.

摘要

许多癌症疗法会产生毒副作用,其分子机制仍有待充分阐明。化疗药物最令人恐惧和研究的副作用是心脏毒性。此外,许多化疗治疗后也记录到骨骼肌生理学损伤。然而,只有阿霉素被广泛研究其对骨骼肌的副作用。在许多情况下,化疗引起的不良反应是由线粒体损伤介导的。特别是曲妥珠单抗和舒尼替尼的毒性主要与线粒体损伤有关,且大多是可逆的。相反,阿霉素引起的毒性不仅包括线粒体损伤,还可导致更严重和广泛的细胞损伤,通常是不可逆和致命的。干扰线粒体功能的药物会导致 ATP 储备枯竭,并导致随后的可逆收缩功能障碍。线粒体损伤包括呼吸链的损伤和线粒体膜电位的丧失,随后会破坏细胞能量。在应激增加的情况下,AMPK 在维持能量平衡方面起着关键作用,抑制 AMPK 途径是介导化疗药物引起的线粒体毒性的一种可能机制。针对细胞代谢和能量管理的治疗方法可能是保护肌肉组织免受化疗药物毒性的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/5878876/dbe49a1be809/OMCL2018-7582730.001.jpg

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