Department of Biology, Biotechnical Faculty, University of Ljubljana, 1000 Ljubljana, Slovenia.
Mar Drugs. 2013 Jul 16;11(7):2574-94. doi: 10.3390/md11072574.
Naturally occurring 3-alkylpyridinium polymers (poly-APS) from the marine sponge Reniera sarai, consisting of monomers containing polar pyridinium and nonpolar alkyl chain moieties, have been demonstrated to exert a wide range of biological activities, including a selective cytotoxicity against non-small cell lung cancer (NSCLC) cells. APS8, an analog of poly-APS with defined alkyl chain length and molecular size, non-competitively inhibits α7 nicotinic acetylcholine receptors (nAChRs) at nanomolar concentrations that are too low to be acetylcholinesterase (AChE) inhibitory or generally cytotoxic. In the present study we show that APS8 inhibits NSCLC tumor cell growth and activates apoptotic pathways. APS8 was not toxic for normal lung fibroblasts. Furthermore, in NSCLC cells, APS8 reduced the adverse anti-apoptotic, proliferative effects of nicotine. Our results suggest that APS8 or similar compounds might be considered as lead compounds to develop antitumor therapeutic agents for at least certain types of lung cancer.
海洋海绵 Reniera sarai 中天然存在的 3-烷基吡啶鎓聚合物(poly-APS),由含有极性吡啶鎓和非极性烷基链部分的单体组成,已被证明具有广泛的生物活性,包括对非小细胞肺癌(NSCLC)细胞的选择性细胞毒性。APS8 是 poly-APS 的类似物,具有确定的烷基链长度和分子大小,在纳摩尔浓度下非竞争性抑制α7 烟碱型乙酰胆碱受体(nAChRs),该浓度太低,不足以抑制乙酰胆碱酯酶(AChE)或具有一般细胞毒性。在本研究中,我们表明 APS8 抑制 NSCLC 肿瘤细胞生长并激活凋亡途径。APS8 对正常肺成纤维细胞没有毒性。此外,在 NSCLC 细胞中,APS8 降低了尼古丁的不良抗凋亡、增殖作用。我们的结果表明,APS8 或类似化合物可能被认为是开发抗肿瘤治疗剂的先导化合物,至少对某些类型的肺癌是如此。