Bioprospection and Product Development Division, CSIR-Central Institute of Medicinal and Aromatic Plants, Lucknow 226015, Uttar Pradesh, India; Academy of Scientific & Innovative Research (AcSIR), Ghaziabad 201002, Uttar Pradesh, India.
Department of Applied Sciences, Indian Institute of Information Technology Allahabad, Prayagraj, Uttar Pradesh, India.
Biochim Biophys Acta Gen Subj. 2023 Jun;1867(6):130340. doi: 10.1016/j.bbagen.2023.130340. Epub 2023 Mar 2.
Triple-negative breast cancer (TNBC) accounts for 20% of breast cancer that does not express HER2, progesterone and estrogen receptors. It is associated with a high mortality rate, morbidity, metastasis, recurrence, poor prognosis and resistance to chemotherapy. Lipoxygenase-5 (LOX-5), cyclooxygenase-2 (COX-2), cathepsin-D (CATD), ornithine decarboxylase (ODC) and dihydrofolate reductase (DHFR) are involved in breast cancer carcinogenesis; hence, there is a pressing need to identify novel chemicals that targets these enzymes. Narirutin, a flavanone glycoside abundantly present in citrus fruits, is reported to have immune-modulatory, anti-allergic and antioxidant potential. Still, the cancer chemopreventive mechanism against TNBC has not been explored.
In vitro experiments, enzyme activity, expression analysis, molecular docking and MD simulation were carried out.
Narirutin suppressed the growth of MDA-MB-231 and MCF-7 in a dose-proportional manner. The pronounced effect with >50% inhibition was observed in SRB and MTT assays for MDAMB-231 cells. Unexpectedly, narirutin suppressed the proliferation of normal cells (24.51%) at 100 μM. Further, narirutin inhibits the activity of LOX-5 in cell-free (18.18 ± 3.93 μM) and cell-based (48.13 ± 7.04 μM) test systems while moderately affecting COX-2, CATD, ODC and DHFR activity. Moreover, narirutin revealed a down-regulation of LOX-5 expression with a fold change of 1.23. Besides, MD simulation experiments confirm that narirutin binding forms a stable complex with LOX-5 and improves the stability and compactness of LOX-5. In addition, the prediction analysis demonstrates that narirutin could not cross the blood-brain barrier and did not act as an inhibitor of different CYPs.
Narirutin could be a potent cancer chemopreventive lead for TNBC, further paving the way for synthesizing novel analogues.
三阴性乳腺癌(TNBC)占不表达 HER2、孕激素和雌激素受体的乳腺癌的 20%。它与高死亡率、发病率、转移、复发、预后不良和化疗耐药有关。脂氧合酶-5(LOX-5)、环氧化酶-2(COX-2)、组织蛋白酶-D(CATD)、鸟氨酸脱羧酶(ODC)和二氢叶酸还原酶(DHFR)参与乳腺癌的发生;因此,迫切需要确定针对这些酶的新型化学物质。柚皮苷是柑橘类水果中丰富存在的一种类黄酮糖苷,据报道具有免疫调节、抗过敏和抗氧化潜力。然而,针对 TNBC 的癌症化学预防机制尚未得到探索。
进行了体外实验、酶活性分析、表达分析、分子对接和 MD 模拟。
柚皮苷呈剂量依赖性抑制 MDA-MB-231 和 MCF-7 的生长。在 MDA-MB-231 细胞的 SRB 和 MTT 测定中,观察到 >50%抑制的明显作用。出乎意料的是,柚皮苷在 100μM 时抑制正常细胞(24.51%)的增殖。此外,柚皮苷在无细胞(18.18±3.93μM)和基于细胞的(48.13±7.04μM)测试系统中抑制 LOX-5 的活性,同时适度影响 COX-2、CATD、ODC 和 DHFR 的活性。此外,柚皮苷显示 LOX-5 表达下调,倍数变化为 1.23。此外,MD 模拟实验证实,柚皮苷与 LOX-5 形成稳定的复合物,提高 LOX-5 的稳定性和紧凑性。此外,预测分析表明,柚皮苷不能穿过血脑屏障,也不作为不同 CYP 的抑制剂。
柚皮苷可能是 TNBC 的有效癌症化学预防先导物,进一步为合成新型类似物铺平道路。