Pharmacological Study and Overcome theCardiotoxicity Associated with Anticancer DrugDoxorubicin

Muhammad Zafar, Huma Sabir
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引用次数: 3

Abstract

Doxorubicin, also known as Adriamycin, is an anthracycline drug commonly used in cancer chemotherapy. Adriamycin is being used clinically for solid tumours, e.g. adenocarcinoma of breast, malignant sarcomas, neuroblastoma, ovarian cancer, small lung cancer as well as hematologic malignancies including lymphomas and leukaemias. In this review we can answers different questions from which mainly we focus on that how we can prevent its toxicity and interactions with other agents and which parameters we use for to overcome this. Unfortunately, its therapeutic potential can be limited to cardiotoxicity so for to overcome this liposomal encapsulation of doxorubicin done for to overcome toxicity problems. However its use has been limited by its major clinical side effect, cardiotoxicity. Toxic effect of Adriamycin can be prevented by using different pharmacologic substances like antioxidants. Adriamycin produces its antineoplastic effect by multiple mechanisms and the exact mechanism of action of Adriamycin is still unknown. The proposed mechanism of the antineoplastic effect of Adriamycin at the cellular level is drug binding to DNA by intercalation between base pairs and inhibition of RNA synthesis by template disordering and steric obstruction.
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抗癌药物阿霉素对心脏毒性的药理研究与克服
阿霉素,又称阿霉素,是一种常用于癌症化疗的蒽环类药物。阿霉素在临床上用于治疗实体肿瘤,如乳腺腺癌、恶性肉瘤、神经母细胞瘤、卵巢癌、小肺癌以及包括淋巴瘤和白血病在内的血液恶性肿瘤。在这篇综述中,我们可以回答不同的问题,我们主要关注的是如何预防其毒性和与其他药物的相互作用以及我们使用哪些参数来克服这一点。不幸的是,它的治疗潜力可能局限于心脏毒性,因此为了克服阿霉素的脂质体包封是为了克服毒性问题。然而,由于其主要的临床副作用——心脏毒性,它的使用受到限制。阿霉素的毒性作用可以通过使用抗氧化剂等不同的药理物质来预防。阿霉素的抗肿瘤作用机制多种多样,其确切作用机制尚不清楚。在细胞水平上,阿霉素抗肿瘤作用的机制可能是药物通过插入碱基对与DNA结合,并通过模板紊乱和位阻抑制RNA合成。
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