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作为一种辅助治疗方式,褪黑素与阿霉素联合应用。

Melatonin as an adjuvant treatment modality with doxorubicin.

机构信息

Research Center for Biochemistry and Nutrition in Metabolic Diseases, Institute for Basic Sciences, Kashan University of Medical Sciences, Kashan, I.R Iran.

Department of Cell Systems and Anatomy, UT Health. Long School of Medicine, San Antonio, TX, USA.

出版信息

Biochimie. 2022 Nov;202:49-55. doi: 10.1016/j.biochi.2022.06.007. Epub 2022 Jun 22.

Abstract

Combination chemotherapy seems to be a beneficial choice for some cancer patients particularly when the drugs target different processes of oncogenesis; patients treated with combination therapies sometimes have a better prognosis than those treated with single drug chemotherapy. However, research has shown that this is not always the case, and this approach may only increase toxicity without having a significant effect in augmenting the antitumor actions of the drugs. Doxorubicin (Dox) is one of the most common chemotherapy drugs used to treat many types of cancer, but it also has serious side effects, such as cardiotoxicity, skin necrosis, testicular toxicity, and nephrotoxicity. Many studies have examined the efficiency of melatonin (MLT) as an anticancer agent. In fact, MLT is an anti-cancer agent that has various functions in inhibiting cancer cell proliferation, inducing apoptosis, and suppressing metastasis. Herein, we provide a comprehensive evaluation of the literature concerned with the role of MLT as an adjuvant in Dox-based chemotherapies and discuss how MLT may enhance the antitumor effects of Dox (e.g., by inducing apoptosis and suppressing metastasis) while rescuring other organs from its adverse effects, such as cardio- and nephrotoxicity.

摘要

联合化疗似乎是某些癌症患者的有益选择,特别是当药物针对肿瘤发生的不同过程时;接受联合治疗的患者的预后有时比接受单一药物化疗的患者要好。然而,研究表明情况并非总是如此,这种方法可能只会增加毒性,而不会显著增强药物的抗肿瘤作用。多柔比星(Dox)是最常用于治疗多种癌症的化疗药物之一,但它也有严重的副作用,如心脏毒性、皮肤坏死、睾丸毒性和肾毒性。许多研究已经研究了褪黑素(MLT)作为抗癌药物的功效。事实上,MLT 是一种抗癌剂,在抑制癌细胞增殖、诱导细胞凋亡和抑制转移方面具有多种功能。在此,我们对 MLT 作为基于 Dox 的化疗辅助剂的作用的文献进行了全面评估,并讨论了 MLT 如何增强 Dox 的抗肿瘤作用(例如,通过诱导细胞凋亡和抑制转移),同时减轻其他器官的不良反应,如心脏毒性和肾毒性。

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