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Jasmonates: Plant Stress Hormones as Anticancer Agents

机译:茉莉花:植物抗逆激素作为抗癌药。

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Jasmonates are a group of plant stress hormones which are among the most potent regulators of defense-related mechanisms in plants. In recent years, several groups have reported that jasmonates are endowed with anti-cancer activities both in vitro and in vivo. Jasmonates were shown to induce death and inhibit the proliferation and the migration of various cancer cell types, including drug-resistant cells. Moreover, jasmonates were shown to impair the angiogenic process, which is essential for tumor progression. In line with their anti-cancer activities in vitro, jasmonates were shown to increase the survival of lymphoma-bearing mice and to inhibit the development of lung metastases in a mouse melanoma model. Importantly, jasmonates are highly selective towards cancer cells and have little or no effect on normal cells, creating a wide therapeutic window. Recently, a first-in-man study demonstrated that methyl jasmonate has a beneficial effect in treating human pre-cancerous and cancerous skin lesions. Several mechanisms were shown to mediate the anti-cancer activities of jasmonates. These include: direct perturbation of mitochondria, production of reactive oxygen species, induction of cellular differentiation, inhibition of aldo-keto reductases, upregulation of several pro-apoptotic proteins and downregulation of anti-apoptotic proteins. A number of research groups have taken the natural jasmonate compounds as a starting point to prepare and evaluate a wide variety of synthetic jasmonate derivatives. Several of these derivatives exhibited enhanced anti-cancer activities in vitro and in vivo. While the vast majority of studies on jasmonates as potential drugs have been performed in the cancer arena, these compounds have also been evaluated as anti-parasitic and anti-inflammatory agents. In conclusion, jasmonates present a unique class of anti-cancer compounds which deserves continued research at the basic, pharmaceutical and clinical levels in order to yield novel chemotherapeutic agents against a range of neoplastic diseases.
机译:茉莉酸酯是一组植物胁迫激素,是植物防御相关机制中最有效的调节剂之一。近年来,几组报道茉莉酸酯在体外和体内均具有抗癌活性。茉莉酸酯显示出诱导死亡并抑制包括癌细胞在内的多种癌细胞类型的增殖和迁移。此外,茉莉酸酯显示出损害血管生成过程,这对于肿瘤的进展至关重要。与其茉莉酸酯的体外抗癌活性一致,茉莉酸酯显示出可增加荷瘤小鼠的存活率并抑制小鼠黑色素瘤模型中肺转移的发展。重要的是,茉莉酸酯对癌细胞具有高度选择性,并且对正常细胞几乎没有影响,甚至没有影响,从而创造了广阔的治疗窗口。最近,一项首次人体研究证明,茉莉酸甲酯在治疗人类癌前期和癌前皮肤病变中具有有益作用。已显示出几种机制来介导茉莉酸酯的抗癌活性。这些措施包括:线粒体的直接摄动,活性氧的产生,细胞分化的诱导,醛基酮还原酶的抑制,几种促凋亡蛋白的上调和抗凋亡蛋白的下调。许多研究小组已将天然茉莉酸酯化合物作为制备和评估各种合成茉莉酸酯衍生物的起点。这些衍生物中的几种在体外和体内均表现出增强的抗癌活性。尽管在癌症领域已经对茉莉酸酯作为潜在药物进行了绝大多数研究,但这些化合物也被评估为抗寄生虫和抗炎药。总之,茉莉酸酯类化合物是一类独特的抗癌化合物,值得在基础,药物和临床水平上进行持续研究,以生产针对多种肿瘤疾病的新型化学治疗剂。

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