Tyagi Garima, Kapoor Neha, Chandra Girish, Gambhir Lokesh
Department of Biotechnology, School of Basic & Applied Sciences, Shri Guru Ram Rai University, Dehradun, Uttrakhand 248001 India.
School of Applied Sciences, Suresh Gyan Vihar University, Jaipur, Rajasthan 302017 India.
3 Biotech. 2021 Jun;11(6):263. doi: 10.1007/s13205-021-02803-x. Epub 2021 May 12.
Success of targeted cancer treatment modalities has generated an ambience of plausible cure for cancer. However, cancer remains to be the major cause of mortality across the globe. The emergence of chemoresistance, relapse after treatment and associated adverse effects has posed challenges to the present therapeutic regimes. Thus, investigating new therapeutic agents of natural origin and delineating the underlying mechanism of action is necessary. Since ages and still in continuum, the phytochemicals have been the prime source of identifying bioactive agents against cancer. They have been exploited for isolating targeted specific compounds to modulate the key regulating signaling pathways of cancer pathogenesis and progression. Capsaicin (alkaloid compound in chilli), catechin, epicatechin, epigallocatechin and epigallocatechin-3-gallate (phytochemicals in green tea), lutein (carotenoid found in yellow fruits), Garcinol (phenolic compound present in kokum tree) and many other naturally available compounds are also very valuable to develop the drugs to treat the cancer. An alternate repository of similar chemical diversity exists in the form of endophytic fungi inhabiting the medicinal plants. There is a high diversity of plant associated endophytic fungi in nature which are potent producers of anti-cancer compounds and offers even stronger hope for the discovery of an efficient anti-cancer drug. These fungi provide various bioactive molecules, such as terpenoids, flavonoids, alkaloids, phenolic compounds, quinines, steroids etc. exhibiting anti-cancerous property. The review discusses the relevance of phytochemicals in chemoprevention and as modulators of miRNA. The perspective advocates the imperative role of anti-cancerous secondary metabolites containing repository of endophytic fungi, as an alternative route of drug discovery.
靶向癌症治疗方式的成功营造出了一种癌症有望治愈的氛围。然而,癌症仍是全球主要的致死原因。化疗耐药性的出现、治疗后的复发以及相关副作用给当前的治疗方案带来了挑战。因此,研究天然来源的新型治疗药物并阐明其潜在作用机制是必要的。自古以来且至今仍在持续,植物化学物质一直是鉴定抗癌生物活性药物的主要来源。它们已被用于分离靶向特定化合物,以调节癌症发病机制和进展的关键调控信号通路。辣椒素(辣椒中的生物碱化合物)、儿茶素、表儿茶素、表没食子儿茶素和表没食子儿茶素 -3- 没食子酸酯(绿茶中的植物化学物质)、叶黄素(黄色水果中发现的类胡萝卜素)、藤黄果醇(罗望子树中存在的酚类化合物)以及许多其他天然可得的化合物对于开发抗癌药物也非常有价值。以栖息于药用植物中的内生真菌形式存在着一个具有类似化学多样性的替代资源库。自然界中与植物相关的内生真菌具有高度多样性,它们是抗癌化合物的有效生产者,为发现高效抗癌药物提供了更强的希望。这些真菌提供了各种具有抗癌特性的生物活性分子,如萜类化合物、黄酮类化合物、生物碱、酚类化合物、奎宁、甾体等。本文综述讨论了植物化学物质在化学预防以及作为微小 RNA 调节剂方面的相关性。该观点主张含有内生真菌资源库的抗癌次生代谢产物作为药物发现的替代途径所起的重要作用。