Roomi Mohd Waheed, Kalinovsky Tatiana, Rath Matthias, Niedzwiecki Aleksandra
Dr. Rath Research Institute, Santa Clara, CA, 95050, USA.
Nutrients. 2017 Mar 18;9(3):303. doi: 10.3390/nu9030303.
Ovarian cancer is the deadliest gynecological malignancy in women, and fifth leading cause of death. Despite advances made in chemotherapy and surgery, the average time of clinical remission is approximately 2 years and the 5-year survival rate is 45%. Thus, there is an urgent need for the development of a novel therapeutic approach to ovarian cancer treatment. We investigated the effect of a specific nutrient mixture (EPQ) containing ascorbic acid, lysine, proline, green tea extract, and quercetin on human ovarian cancer cell A-2780 in vivo and in vitro. Athymic female nude mice (n = 12) were all inoculated intraperitoneally (IP) with 2 × 10⁶ cells in 0.1 mL of phosphate buffered saline (PBS) and randomly divided into two groups. Upon injection, the Control group (n = 6) was fed a regular diet and the EPQ group (n = 6) a regular diet supplemented with 0.5% EPQ. Four weeks later, the mice were sacrificed and tumors that developed in the ovary were excised, weighed, and processed for histology. Lungs were inspected for metastasis. In vitro, A-2780 cells were cultured in Dulbecco modified Eagle medium supplemented with 10% FBS and antibiotics. At near confluence, cells were treated with EPQ in triplicate at concentrations between 0 and 1000 μg/mL. Cell proliferation was measured via MTT assay, MMP-9 secretion via gelatinase zymography, invasion through Matrigel and morphology via hematoxylin and eosin (H & E) staining. All Control mice developed large ovarian tumors, whereas 5 out of 6 mice in the EPQ group developed no tumors, and one, a small tumor. Control mice also showed lung metastasis in 6 out of 6 mice, while no lung metastasis was evident in EPQ mice. Zymography demonstrated only MMP-9 expression, which EPQ inhibited in a dose-dependent fashion, with virtual total block at 250 μg/mL concentration. EPQ significantly inhibited invasion through Matrigel with total block at 250 μg/mL concentration. MTT showed dose-dependent inhibition of cell proliferation with EPQ, and H & E staining showed no morphological changes below 500 μg/mL EPQ. These results suggest that EPQ has therapeutic potential in the treatment of ovarian cancer by significantly suppressing ovarian tumor incidence and growth and lung metastasis, and by inhibiting MMP-9 secretion and invasion of A-2780 ovarian cancer cells.
卵巢癌是女性中最致命的妇科恶性肿瘤,也是第五大致死原因。尽管在化疗和手术方面取得了进展,但临床缓解的平均时间约为2年,5年生存率为45%。因此,迫切需要开发一种新的卵巢癌治疗方法。我们研究了一种特定的营养混合物(EPQ),其包含抗坏血酸、赖氨酸、脯氨酸、绿茶提取物和槲皮素,对人卵巢癌细胞A-2780在体内和体外的作用。无胸腺雌性裸鼠(n = 12)均通过腹腔注射(IP)接种0.1 mL磷酸盐缓冲盐水(PBS)中含有的2×10⁶个细胞,并随机分为两组。注射后,对照组(n = 6)给予常规饮食,EPQ组(n = 6)给予补充有0.5% EPQ的常规饮食。四周后,处死小鼠,切除卵巢中长出的肿瘤,称重,并进行组织学处理。检查肺部是否有转移。在体外,A-2780细胞在补充有10%胎牛血清和抗生素的杜尔贝科改良伊格尔培养基中培养。接近汇合时,细胞以0至1000 μg/mL的浓度一式三份用EPQ处理。通过MTT法测量细胞增殖,通过明胶酶谱法测量MMP-9分泌,通过基质胶测量侵袭,并通过苏木精和伊红(H&E)染色观察形态。所有对照组小鼠都长出了大的卵巢肿瘤,而EPQ组6只小鼠中有5只未长出肿瘤,1只长出了小肿瘤。对照组小鼠在6只中有6只出现了肺转移,而EPQ组小鼠中未发现明显的肺转移。酶谱分析仅显示MMP-9表达,EPQ以剂量依赖性方式抑制该表达,在250 μg/mL浓度时几乎完全阻断。EPQ在250 μg/mL浓度时显著抑制通过基质胶的侵袭。MTT显示EPQ对细胞增殖有剂量依赖性抑制作用,H&E染色显示在500 μg/mL EPQ以下无形态学变化。这些结果表明,EPQ通过显著抑制卵巢肿瘤的发生率、生长和肺转移,以及抑制A-2780卵巢癌细胞的MMP-9分泌和侵袭,在卵巢癌治疗中具有治疗潜力。