Marine Compounds Selectively Induce Apoptosis in Female Reproductive Cancer Cells but Not in Primary-Derived Human Reproductive Granulosa Cells

被引:35
|
作者
Edwards, Vicki [3 ]
Benkendorff, Kirsten [1 ,2 ]
Young, Fiona [3 ]
机构
[1] Flinders Univ S Australia, Sch Biol Sci, Adelaide, SA 5001, Australia
[2] So Cross Univ, Sch Environm Sci & Management, Lismore, NSW 2480, Australia
[3] Flinders Univ S Australia, Sch Med, Dept Med Biotechnol, Adelaide, SA 5001, Australia
来源
MARINE DRUGS | 2012年 / 10卷 / 01期
关键词
gynaecological cancers; brominated indoles; marine mollusc; apoptosis; TYRIAN PURPLE PRECURSORS; PHASE-II TRIAL; NATURAL-PRODUCTS; OVARIAN-CARCINOMA; SIGNALING PATHWAYS; DRUG DISCOVERY; DEATH; PROLIFERATION; CYTOTOXICITY; INHIBITION;
D O I
10.3390/md10010064
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Anticancer properties of tyrindoleninone and 6-bromoisatin from Dicathais orbita were tested against physiologically normal primary human granulosa cells (HGC) and reproductive cancer cell lines. Tyrindoleninone reduced cancer cell viability with IC50 values of 39 mu M (KGN; a tumour-derived granulosa cell line), 39 mu M (JAr), and 156 mu M (OVCAR-3), compared to 3516 mu M in HGC. Apoptosis in HGC's occurred after 4 h at 391 mu M tyrindoleninone compared to 20 mu M in KGN cells. Differences in apoptosis between HGC and KGN cells were confirmed by TUNEL, with 66 and 31% apoptotic nuclei at 4 h in KGN and HGC, respectively. These marine compounds therefore have potential for development as treatments for female reproductive cancers.
引用
收藏
页码:64 / 83
页数:20
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