白云木根叶提取物对埃利希腹水癌(EAC)细胞的体内抗癌活性研究

M. Bhat, F. Khan, Harish Chand Kataria
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摘要

癌症是一种细胞生长失控的疾病。目前可用的治疗方法有放疗、化疗、激素治疗和手术,但这些方法都有副作用。由于不良的副作用,开发新的癌症治疗药物是一个挑战。因此,科学家们正试图从天然来源中寻找治疗癌症的化合物。因此,本研究以菊树根、叶提取物为研究材料,对其在埃利希腹水癌(EAC)细胞系中的抗增殖作用及凋亡分子信号传导进行了研究。与标准的抗氧化剂BHT相比,苦楝根和叶提取物显示出相当大的清除活性。此外,根和叶提取物能够凝集2%的山羊血RBC,浓度分别为12.5g/mL和50.0g/mL。在根和叶提取物中也发现细胞毒活性。在造血观察中,根提取物和叶提取物的细胞生长抑制率分别为62.54±2.41%和53.96±2.34%,而抗癌标准药物博来霉素的细胞生长抑制率为79.43±1.92%。荧光显微镜下形态学变化显示细胞核凝聚和碎裂,是细胞凋亡的标志。因此,目前的研究结果表明,白云木根提取物对EAC细胞系具有抗增殖活性,可以作为治疗癌症的良好抗癌药物来源。
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In-vivo Anticancer Activity of Root and Leaf extract of Jurinea dolomiaea Boiss (Asteraceae) against Ehrlichs Ascites Carcinoma (EAC) Cell Line
Cancer is a type of disease of uncontrolled growth cells. The currently available treatments are radiotherapy, chemotherapy, hormone therapy and surgery, in which all of them have side effects. Due to the adverse side effects, it is challenging to develop new drug for cancer treatment. Hence, the scientists are trying to seek the compounds from natural sources to treat cancer. Therefore, in this present investigation, root and leaf extracts of Jurinea dolomiaea Boiss has subjected to evaluate its anti-proliferative effect along with molecular signaling of apoptosis in Ehrlich ascites carcinoma (EAC) cell line. Jurinea dolomiaea root and leaf extracts exhibit a considerable scavenging activity in comparison to a standard antioxidant BHT. Moreover, root and leaf extracts were able to agglutinate 2% RBC of goat blood at minimum 12.5 g/mL and 50.0 g/mL concentration respectively. Cytotoxic activity was also found in root and leaf extract. In haemocytometic observation, the root and leaf extract exhibit about 62.54±2.41% and 53.96±2.34% cell growth inhibition respectively where as standard anticancer drug Bleomycin showed 79.43±1.92% growth inhibition. Morphological change under fluorescence microscope showed nuclear condensation and fragmentation which are the sign of apoptosis. Therefore, current results depict root extract of Jurinea dolomiaea Boiss have anti-proliferative activity against EAC cell line and can be a good source of anticancer agents to treat cancer.
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