Chui Chung Hin, Tang Johnny Cheuk On, Lau Fung Yi, Teo Ivy Tuang Ngo, Yau Mable Yin Chun, Wong Raymond Siu Ming, Cheng Gregory Yin Ming, Ho Stephen King Wah, Leung Thomas Wai Tong, Hui Kin Shing, Wong Mai Man, Fatima Sarwat, Cheng Chor Hing, Cheung Filly, Tan Wei Qi, Chow Larry Ming Cheung, Guo Dean, Chan Albert Sun Chi
Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong, PR China.
Int J Mol Med. 2004 Jan;13(1):169-73.
Recently we have shown the antiproliferative activity of Gleditsia sinensis fruit extract (GSE) on various solid tumour and leukaemia cell lines as well as primary cultured bone marrow cells isolated from patients with acute and chronic myelogenous leukaemia. We further studied whether the growth inhibitory effect of GSE involves basic fibroblast growth factor (bFGF) in cancer cell lines including breast cancer MDA-MB231, nasopharyngeal cancer CNE-2 and prostate cancer LNCaP. We also investigated whether GSE could alter the production of nitric oxide (NO) pattern from these cancer cell lines. Growth inhibition assay was quantitated by sulforhodamine B protein staining method. Enzyme linked immunosorbent assay (ELISA) was used to quantitate the total bFGF protein. The amount of NO secreted into culture medium in terms of nitrite ion concentration was measured by the Greiss method. ELISA showed that GSE could stimulate total bFGF protein level which was dose- dependent. NO production was also stimulated from these cancer cell lines after treating with GSE. Both of the increment in total bFGF and NO levels were correlated with the degree of growth inhibition. Changes involving cell shrinkage and detachment of cancer cells could readily be observed. Taken together, our results here suggest that growth inhibition induced by GSE in these solid tumour cell lines may involve both bFGF and NO regulations.
最近我们已经证明,皂荚果实提取物(GSE)对各种实体瘤和白血病细胞系以及从急性和慢性粒细胞白血病患者分离出的原代培养骨髓细胞具有抗增殖活性。我们进一步研究了GSE对癌细胞系(包括乳腺癌MDA-MB231、鼻咽癌CNE-2和前列腺癌LNCaP)的生长抑制作用是否涉及碱性成纤维细胞生长因子(bFGF)。我们还研究了GSE是否能改变这些癌细胞系中一氧化氮(NO)的产生模式。生长抑制试验采用磺基罗丹明B蛋白染色法进行定量。酶联免疫吸附测定(ELISA)用于定量总bFGF蛋白。采用格里斯法测定培养基中亚硝酸盐离子浓度表示的分泌到培养基中的NO量。ELISA显示GSE能刺激总bFGF蛋白水平,且呈剂量依赖性。用GSE处理后,这些癌细胞系也能刺激NO的产生。总bFGF和NO水平的增加均与生长抑制程度相关。可以很容易地观察到癌细胞出现细胞收缩和脱离等变化。综上所述,我们的研究结果表明,GSE在这些实体瘤细胞系中诱导的生长抑制可能涉及bFGF和NO的调节。