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In Vitro and In Vivo Anticancer Activity of Root Extracts of Sansevieria liberica Gerome and Labroy (Agavaceae)

机译:虎尾兰Gerome和Labroy(Agavaceae)根提取物的体外和体内抗癌活性

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摘要

Introduction. Sansevieria liberica Gerome and Labroy (Agavaceae) is a perennial plant widely distributed in tropical Africa. Preparations of the plant are commonly used across Nigeria for the treatment of inflammatory conditions. Based on the fact that herbal medicine is a strong component of integrative medicine, this study was conducted to evaluate the anticancer activity of root extracts of Sansevieria liberica. Methods. Sulforhodamine B (SRB) in vitro cytotoxicity assay, Sarcoma-180 (S-180) ascites and solid tumor, and L1210 lymphoid leukemia in vivo models were used in this study. Results. SL-A002 (IC50 23 µg/mL with HeLa), SL-A003 (IC50 22 µg/mL with HCT-116), and SL-A004 (IC50 23 and 18 µg/mL with A549 and THP-1, resp.) demonstrated significant activity in the SRB cytotoxicity assay. Potency was highest with the following pairs of extract : cancer cell line: SL-A002 : HeLa (IC50 23 µg/mL), SL-A003 : HCT-116 (IC50 22 µg/mL), and SL-A004 : THP-1 (IC50 18 µg/mL). SL-A002 demonstrated significant dose-dependent antitumor activity in the Sarcoma-180 (S-180) ascites model with peak effect produced at the dose of 120 mg/kg (i.p.) with inhibition of 89.36% compared to 97.96% for 5-FU (20 mg/kg i.p.). The inhibition of tumor growth by SL-A002 in the S-180 solid tumor model was 47.40% compared to a value of 50.18% for 5-FU. SL-A002 was also significantly active in the L1210 lymphoid leukemia model with 158.33% increase in mean survival time, the same value for 5-FU. Conclusions. The hydroethanolic extract of Sansevieria liberica, SL-A002, possesses significant anticancer activity to warrant further extensive study to identify, isolate, and characterize the specific bioactive molecules responsible for the observed antitumor activity and the precise mechanism(s) of action.
机译:介绍。虎尾兰Gerome and Labroy(Agavaceae)是多年生植物,广泛分布于热带非洲。该植物的制剂在整个尼日利亚普遍用于治疗炎症。基于草药是中西医结合剂的重要组成部分这一事实,本研究旨在评估虎尾草根提取物的抗癌活性。方法。在这项研究中使用了磺胺多巴酚B(SRB)的体外细胞毒性测定,肉瘤180(S-180)腹水和实体瘤以及L1210淋巴样白血病的体内模型。结果。 SL-A002(含HeLa的IC50为23µµg / mL),SL-A003(含HCT-116的IC50为22µµg / mL)和SL-A004(A549和THP-1的IC50为23µg / mL)。在SRB细胞毒性测定中显示出显着的活性。以下几对提取物的效价最高:癌细胞系:SL-A002:HeLa(IC50 23μg/ mL),SL-A003:HCT-116(IC50 22μg/ mL)和SL-A004:THP-1 (IC50 18 µg / mL)。 SL-A002在肉瘤180(S-180)腹水模型中显示出显着的剂量依赖性抗肿瘤活性,在120μmg/ kg(ip)剂量下产生峰值效应,抑制率为89.36%,而5-FU抑制率为97.96% (20 mg / kg ip)。 SL-A002在S-180实体瘤模型中对肿瘤生长的抑制作用为47.40%,而5-FU的抑制率为50.18%。 SL-A002在L1210淋巴白血病模型中也具有显着活性,平均生存时间增加158.33%,与5-FU值相同。结论。解放军虎杖的乙醇乙醇提取物SL-A002具有显着的抗癌活性,需要进一步的广泛研究以鉴定,分离和表征负责观察到的抗肿瘤活性和确切作用机理的特定生物活性分子。

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