Programa de Pós-graduação em Biologia Celular e Estrutural, Instituto de Biologia, Universidade Estadual de Campinas - UNICAMP, Campinas, SP, Brasil.
Planta Med. 2011 Sep;77(13):1482-8. doi: 10.1055/s-0030-1270889. Epub 2011 Mar 9.
Despite numerous studies with the Piper genus, there are no previous results reporting in vitro or in vivo Piper regnellii (Miq.) C. DC. var. regnellii anticancer activity. The aim of this study was to investigate P. regnellii in vitro and in vivo anticancer activity and further identify its active compounds. In vitro antiproliferative activity was evaluated in 8 human cancer cell lines: melanoma (UACC-62), breast (MCF7), kidney (786-0), lung (NCI-H460), prostate (PC-3), ovary (OVCAR-3), colon (HT29), and leukemia (K-562). Total growth inhibition (TGI) values were chosen to measure antiproliferative activity. Among the cell lines evaluated, eupomatenoid-5 demonstrated better in vitro antiproliferative activity towards prostate, ovary, kidney, and breast cancer cell lines. In vivo studies were carried out with Ehrlich solid tumor on Balb/C mice treated with 100, 300, and 1000 mg/kg of P. regnellii leaves dichloromethane crude extract (DCE), with 30 and 100 mg/kg of the active fraction (FRB), and with 30 mg/kg of eupomatenoid-5. The i. p. administration of DCE, FRB, and eupomatenoid-5 significantly inhibited tumor progression in comparison to control mice (saline). Therefore, this study showed that neolignans of Piper regnellii have promising anticancer activity. Further studies will be undertaken to determine the mechanism of action and toxicity of these compounds.
尽管对胡椒属进行了大量研究,但目前尚无关于 Piper regnellii(Miq.)C. DC. var. regnellii 的体外或体内抗癌活性的研究结果。本研究旨在研究 Piper regnellii 的体外和体内抗癌活性,并进一步鉴定其活性化合物。在 8 个人类癌细胞系中评估了体外增殖抑制活性:黑色素瘤(UACC-62)、乳腺癌(MCF7)、肾细胞癌(786-0)、肺癌(NCI-H460)、前列腺癌(PC-3)、卵巢癌(OVCAR-3)、结肠癌(HT29)和白血病(K-562)。总生长抑制(TGI)值用于测量增殖抑制活性。在所评估的细胞系中,eupomatenoid-5 对前列腺癌、卵巢癌、肾癌和乳腺癌细胞系表现出更好的体外增殖抑制活性。在使用 Ehrlich 实体瘤的 Balb/C 小鼠体内研究中,用 100、300 和 1000 mg/kg 的 Piper regnellii 叶二氯甲烷粗提取物(DCE)、30 和 100 mg/kg 的活性部分(FRB)以及 30 mg/kg 的 eupomatenoid-5 进行治疗。DCE、FRB 和 eupomatenoid-5 的 i.p. 给药与生理盐水对照小鼠相比显著抑制肿瘤进展。因此,本研究表明,Piper regnellii 的新木脂素具有有前途的抗癌活性。将进一步开展研究以确定这些化合物的作用机制和毒性。