摘要
目的研究非毒性分化诱导剂苯乙酸钠(NaPA)在体外对卵巢癌3AO细胞的生长、分化以及表型的影响。方法以3H-TdR参入法和半固体琼脂培养法分别检测了卵巢癌3AO细胞的着壁依赖性和着壁不依赖性生长。以酶联吸附试验(ELISA)检测了3AO细胞表面人白细胞抗原(HLA)Ⅰ、Ⅱ类分子的表达。以电子显微镜观察了3AO细胞的超微结构。结果(1)NaPA能够抑制3AO细胞的着壁依赖性和着壁不依赖性生长,而对正常羊膜组织Wish细胞的生长无显著抑制作用。(2)NaPA能够增强3AO细胞表面HLAⅠ、Ⅱ类分子的表达。(3)以电子显微镜观察到:在NaPA处理的3AO细胞中,线粒体、内质网以及弹力丝等丰富;而在NaPA未处理的3AO细胞中,除了大量游离的多聚核糖体之外,上述的细胞结构几乎没有。结论NaPA不仅能够选择性抑制卵巢癌细胞的生长,而且能够有效地诱导卵巢癌细胞的分化以及表型转变,为NaPA分化治疗卵巢癌提供了实验依据。
AIM The effect of a nontoxic differentiation inducer, sodium phenylacetate (NaPA) on the growth, differentiation and phenotype of ovarian cancer 3AO cells in vitro was studied. METHODS The anchoragedependent and anchorageindependent growth of 3AO cells were evaluated using 3H thymidine incorporation assay and semisolid agar culture assay respectively. The expression of human leucocyte antigen (HLA) class Ⅰ and Ⅱ molecules on the surface of 3AO cells was measured using enzymelinked immunosorbent assay. The ultrastructure of 3AO cells was investigated by electron microscopy. RESULTS (1) NaPA treatment resulted in dosedependent inhibition of 3AO cell growth, including anchoragedependent and anchorageindependent growth. But NaPA was not significantly efficient to inhibitory to the growth of Wish cells from normal amnion tissue. (2) NaPA could enhance the expression of HLA class Ⅰ and Ⅱ molecules on the surface of 3AO cells. (3) Electron micrographs of NaPAtreated 3AO cells demonstrated the emergence of rich mitochondria, rough endoplasmic reticulum and elastic filament, in contrast to the scant beforementioned structures but numerous scattered polyribosomes in NaPAuntreated 3AO cells. CONCLUSION NaPA not only selectively inhibits the growth of ovarian cancer cells, but also is effective in inducing the differentiation and phenotypical modification of ovarian cancer cells. It suggests that NaPA may be potential in the differentiation therapy of ovarian cancer.
出处
《中国药理学通报》
CAS
CSCD
北大核心
1998年第1期56-60,共5页
Chinese Pharmacological Bulletin
基金
上海市高等学校博士点建设基金