Mohsin Ali Khan, Anwar Khan, Akhlak Ahmed Khan, Simrah, Mohd. Aamir Mirza, Kamran Javed Naquvi, Devendra Kumar
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引用次数: 0
Abstract
Nowadays, cancer treatment is currently limited to surgery, chemotherapy, and radiation,
which carry the risk of damaging the normal tissue of the body and incomplete removal of
the cancerous cells from the body. Thus, the Nano technique offers a great means to target therapies
directly on cancerous cells and neoplasm. Moreover, because nano-based formulations of
polyphenolic curcumin show a major effect on cancer and tumour cells, nanoparticles have a tendency
to overcome the hydrophobic nature of curcumin to improve its stability and bioavailability
in vitro and in vivo. It is apparent from the studies that Curcumin has shown anticancer effects by
regulating various immunomodulators, which include cytokines, reactive oxygen species, and
cyclooxygenase-2 (COX-2). It also takes part in the downregulation of growth factors, protein
kinases, oncogenic molecules, and various signalling pathways, such as nuclear factor kappalight-
chain enhancer of activated B cells (NF-κB), c-Jun N-terminal kinase (JNK), and signal
transducer and activator of transcription 3 (STAT3) signalling. According to recent studies and
clinical trials, nano curcumin shows a major effect on cancerous cells. In this article, the authors
summarised the mechanism of nano curcumin in various metastatic cancers and the most recent
clinical trials performed.
目前,癌症的治疗方法仅限于手术、化疗和放疗,但这些方法都有可能损伤人体正常组织,而且不能完全清除体内的癌细胞。因此,纳米技术为直接针对癌细胞和肿瘤的治疗提供了一个很好的手段。此外,由于多酚姜黄素的纳米制剂对癌细胞和肿瘤细胞有重大作用,因此纳米颗粒有克服姜黄素疏水性的趋势,以提高其在体外和体内的稳定性和生物利用度。研究表明,姜黄素通过调节各种免疫调节剂(包括细胞因子、活性氧和环氧化酶-2 (COX-2))而显示出抗癌作用。它还参与下调生长因子、蛋白inkinases、致癌分子和各种信号通路,如活化 B 细胞的核因子 kappalight-chain 增强子(NF-κB)、c-Jun N 端激酶(JNK)和信号转导和激活转录 3(STAT3)信号。根据最近的研究和临床试验,纳米姜黄素对癌细胞有重大作用。在本文中,作者总结了纳米姜黄素在各种转移性癌症中的作用机制以及最新的临床试验。
Current Bioactive CompoundsPharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.90
自引率
0.00%
发文量
112
期刊介绍:
The journal aims to provide comprehensive review articles on new bioactive compounds with proven activities in various biological screenings and pharmacological models with a special emphasis on stereoeselective synthesis. The aim is to provide a valuable information source of bioactive compounds synthesized or isolated, which can be used for further development of pharmaceuticals by industry and academia. The journal should prove to be essential reading for pharmacologists, natural product chemists and medicinal chemists who wish to be kept informed and up-to-date with the most important developments on new bioactive compounds of natural or synthetic origin, including their stereoeselective synthesis.