Department of Pharmacology, Faculty of Medicine, Pavol Jozef Šafárik University, 040 01 Košice, Slovakia.
Int J Mol Sci. 2023 Mar 22;24(6):5964. doi: 10.3390/ijms24065964.
Colorectal (CRC) and gastric cancers (GC) are the most common digestive tract cancers with a high incidence rate worldwide. The current treatment including surgery, chemotherapy or radiotherapy has several limitations such as drug toxicity, cancer recurrence or drug resistance and thus it is a great challenge to discover an effective and safe therapy for CRC and GC. In the last decade, numerous phytochemicals and their synthetic analogs have attracted attention due to their anticancer effect and low organ toxicity. Chalcones, plant-derived polyphenols, received marked attention due to their biological activities as well as for relatively easy structural manipulation and synthesis of new chalcone derivatives. In this study, we discuss the mechanisms by which chalcones in both in vitro and in vivo conditions suppress cancer cell proliferation or cancer formation.
结直肠癌(CRC)和胃癌(GC)是最常见的消化道癌症,全球发病率很高。目前的治疗方法包括手术、化疗或放疗,但存在药物毒性、癌症复发或耐药性等多种局限性,因此,发现一种有效且安全的 CRC 和 GC 治疗方法是一个巨大的挑战。在过去的十年中,由于具有抗癌作用和低器官毒性,许多植物化学物质及其合成类似物引起了人们的关注。查耳酮作为植物来源的多酚,因其生物活性以及相对容易的结构修饰和新查耳酮衍生物的合成而受到广泛关注。在这项研究中,我们讨论了查耳酮在体外和体内条件下抑制癌细胞增殖或肿瘤形成的机制。