Lampronti I, Martello D, Bianchi N, Borgatti M, Lambertini E, Piva R, Jabbar S, Choudhuri M Shahabuddin Kabir, Khan M Tareq Hassan, Gambari R
Department of Biochemistry and Molecular Biology, University of Ferrara, Ferrara, Italy.
Phytomedicine. 2003 May;10(4):300-8. doi: 10.1078/094471103322004794.
In the present paper we show that extracts from Aegle marmelos Correa are able to inhibit the in vitro proliferation of human tumor cell lines, including the leukemic K562, T-lymphoid Jurkat, B-lymphoid Raji, erythroleukemic HEL, melanoma Colo38, and breast cancer MCF7 and MDA-MB-231 cell lines. Molecules present within the studied Aegle marmelos C. extracts were identified by gas-chromatography/mass-spectrometry analysis; three derivatives (butyl p-tolyl sulfide, 6-methyl-4-chromanone and butylated hydroxyanisole) were found to exhibit strong activity in inhibiting in vitro cell growth of human K562 cells. The antiproliferative activity of these compounds was found to be comparable to that of known antitumor agents, including cisplatin, chromomycin, cytosine arabinoside and 5-fluorouracil. In addition, the antiproliferative activity of butyl-p-tolyl sulfide, 6-methyl-4-chromanone and 5-methoxypsolaren was associated to activation of the differentiation pattern of K562 cells.
在本论文中,我们表明,枸橼提取物能够抑制人肿瘤细胞系的体外增殖,这些细胞系包括白血病K562、T淋巴细胞Jurkat、B淋巴细胞Raji、红白血病HEL、黑色素瘤Colo38以及乳腺癌MCF7和MDA-MB-231细胞系。通过气相色谱/质谱分析鉴定了所研究的枸橼提取物中的分子;发现三种衍生物(对甲苯基丁基硫醚、6-甲基-4-色满酮和丁基化羟基茴香醚)在抑制人K562细胞的体外细胞生长方面表现出强大活性。发现这些化合物的抗增殖活性与已知抗肿瘤药物(包括顺铂、色霉素、阿糖胞苷和5-氟尿嘧啶)的抗增殖活性相当。此外,对甲苯基丁基硫醚、6-甲基-4-色满酮和5-甲氧基补骨脂素的抗增殖活性与K562细胞分化模式的激活有关。