Szoka Lukasz, Nazaruk Jolanta, Giegiel Joanna, Isidorov Valery
Department of Medicinal Chemistry, Medical University of Bialystok, Białystok, Poland.
Department of Pharmacognosy, Medical University of Bialystok, Białystok, Poland.
Front Mol Biosci. 2023 Sep 6;10:1247536. doi: 10.3389/fmolb.2023.1247536. eCollection 2023.
Cancer of the corpus uteri and cervix uteri, collectively ranks second among new cancer cases in women after breast cancer. Therefore, investigation of new anticancer agents and identifying new molecular targets presents a challenge to improve effectiveness of chemotherapy. In this study, antiproliferative activity of flavonoids derived from the buds of silver birch and downy birch was evaluated in endometrial cancer Ishikawa cells and cervical cancer HeLa cells. It was found that flavanol santin reduced viability of both cell lines better than other flavonoids, including apigenin and luteolin. Moreover, this activity was slightly higher than that induced by the chemotherapy drug, cisplatin. Santin promoted intrinsic and extrinsic apoptosis pathways in cancer cells, but it had low toxicity in normal fibroblasts. The mechanisms of impairing cancer cell viability included induction of oxidative proline catabolism, however in different ways in the cell lines used. In HeLa cells, increase of proline oxidation was due to activation of p53 leading to proline oxidase upregulation. In contrast, in Ishikawa cells, having basal proline oxidase level significantly higher than HeLa cells, santin treatment decreased its expression. Nevertheless, proline oxidation was induced in these cells since santin increased expression and activity of prolidase, an enzyme providing proline from protein degradation. In both cell lines, proline oxidation was associated with generation of reactive oxygen species leading to reduction in cell viability. Our findings reveal the involvement of proline oxidase in induction of apoptosis by santin and identify a role of prolidase in proline oxidase-dependent apoptosis.
子宫体癌和子宫颈癌加在一起,在女性新发癌症病例中仅次于乳腺癌,位列第二。因此,研发新型抗癌药物并确定新的分子靶点对提高化疗效果构成了挑战。在本研究中,我们评估了源自白桦和毛桦芽的黄酮类化合物对子宫内膜癌Ishikawa细胞和宫颈癌HeLa细胞的抗增殖活性。结果发现,黄烷醇山柰苷比其他黄酮类化合物(包括芹菜素和木犀草素)更能降低这两种细胞系的活力。此外,这种活性略高于化疗药物顺铂诱导的活性。山柰苷可促进癌细胞的内源性和外源性凋亡途径,但对正常成纤维细胞毒性较低。损害癌细胞活力的机制包括诱导氧化脯氨酸分解代谢,但在所使用的细胞系中方式不同。在HeLa细胞中,脯氨酸氧化增加是由于p53激活导致脯氨酸氧化酶上调。相反,在Ishikawa细胞中,其基础脯氨酸氧化酶水平显著高于HeLa细胞,山柰苷处理可降低其表达。然而,这些细胞中仍诱导了脯氨酸氧化,因为山柰苷增加了脯氨肽酶的表达和活性,脯氨肽酶是一种从蛋白质降解中提供脯氨酸的酶。在这两种细胞系中,脯氨酸氧化都与活性氧的产生有关,从而导致细胞活力降低。我们的研究结果揭示了脯氨酸氧化酶参与山柰苷诱导的凋亡,并确定了脯氨肽酶在脯氨酸氧化酶依赖性凋亡中的作用。