Hospital del Centro Gallego de Buenos Aires, Buenos Aires, Argentina.
12357University of Alberta, Edmonton, AB, Canada.
J Evid Based Integr Med. 2022 Jan-Dec;27:2515690X211068826. doi: 10.1177/2515690X211068826.
The flavonoid silymarin extracted from the seeds of is a mixture of 6 flavolignan isomers. The 3 more important isomers are silybin (or silibinin), silydianin, and silychristin. Silybin is functionally the most active of these compounds. This group of flavonoids has been extensively studied and they have been used as hepato-protective substances for the mushroom intoxication and mainly chronic liver diseases such as alcoholic cirrhosis and nonalcoholic fatty liver. Hepatitis C progression is not, or slightly, modified by silymarin. Recently, it has also been proposed for SARS COVID-19 infection therapy. The biochemical and molecular mechanisms of action of these substances in cancer are subjects of ongoing research. Paradoxically, many of its identified actions such as antioxidant, promoter of ribosomal synthesis, and mitochondrial membrane stabilization, may seem protumoral at first sight, however, silymarin compounds have clear anticancer effects. Some of them are: decreasing migration through multiple targeting, decreasing hypoxia inducible factor-1α expression, inducing apoptosis in some malignant cells, and inhibiting promitotic signaling among others. Interestingly, the antitumoral activity of silymarin compounds is limited to malignant cells while the nonmalignant cells seem not to be affected. Furthermore, there is a long history of silymarin use in human diseases without toxicity after prolonged administration. The ample distribution and easy accessibility to milk thistle-the source of silymarin compounds, its over the counter availability, the fact that it is a weed, some controversial issues regarding bioavailability, and being a nutraceutical rather than a drug, has somehow led medical professionals to view its anticancer effects with skepticism. This is a fundamental reason why it never achieved bedside status in cancer treatment. However, in spite of all the antitumoral effects, silymarin actually has dual effects and in some cases such as pancreatic cancer it can promote stemness. This review deals with recent investigations to elucidate the molecular actions of this flavonoid in cancer, and to consider the possibility of repurposing it. Particular attention is dedicated to silymarin's dual role in cancer and to some controversies of its real effectiveness.
水飞蓟素是从水飞蓟种子中提取的一种黄酮类化合物,它是 6 种黄酮木脂素异构体的混合物。其中 3 种更重要的异构体是水飞蓟宾(或水飞蓟宾)、水飞蓟宁和水飞蓟亭。水飞蓟宾在这些化合物中功能最为活跃。这组类黄酮已被广泛研究,并被用作蘑菇中毒和主要慢性肝病(如酒精性肝硬化和非酒精性脂肪肝)的肝保护物质。丙型肝炎的进展不会被水飞蓟素改变,或者只是稍微改变。最近,它也被提议用于治疗严重急性呼吸系统综合征冠状病毒 2 型(SARS-CoV-2)感染。这些物质在癌症中的生化和分子作用机制是正在研究的课题。矛盾的是,其许多已确定的作用,如抗氧化剂、核糖体合成促进剂和线粒体膜稳定化,乍一看似乎具有促肿瘤作用,但水飞蓟素化合物具有明显的抗癌作用。其中一些作用包括:通过多种靶向作用减少迁移、减少缺氧诱导因子-1α 的表达、诱导某些恶性细胞凋亡以及抑制促有丝分裂信号等。有趣的是,水飞蓟素化合物的抗肿瘤活性仅限于恶性细胞,而非恶性细胞似乎不受影响。此外,水飞蓟素在人类疾病中的长期使用历史,且在长期给药后没有毒性。水飞蓟素化合物的广泛分布和易于获得-其来源是奶蓟草,它是非处方药,是一种杂草,关于生物利用度的一些有争议的问题,以及作为一种营养保健品而不是药物,这在某种程度上导致医务人员对其抗癌作用持怀疑态度。这是它从未在癌症治疗中达到床边地位的一个基本原因。然而,尽管有所有的抗肿瘤作用,水飞蓟素实际上具有双重作用,在某些情况下,如胰腺癌,它可以促进干性。本综述涉及最近的研究,以阐明这种类黄酮在癌症中的分子作用,并考虑重新利用它的可能性。特别关注水飞蓟素在癌症中的双重作用以及其实际效果的一些争议。