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An active molecule from Pulsatilla chinensis Pulsatilla saponin A induces apoptosis and inhibits tumor growth of human colon cancer cells without or with 5-FU

机译:来自白头翁的活性分子白头翁皂苷A可以诱导人结肠癌细胞的凋亡并抑制5-FU或不联合5-FU

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摘要

Colon cancer is one of the common types of digestive malignancy. The efficacy of the first-line chemotherapy drug for colon cancer, fluorouracil (5-FU), remains limited in clinical settings due to poor efficacy and significant side effects. In the present study, the anticancer activity of an active compound from Pulsatilla chinensis extracts, Pulsatilla saponin A (PsA), was isolated and examined in vitro and in vivo. It was demonstrated that PsA significantly inhibited the growth of human colon cancer HT-29 cells. This inhibitory activity was also observed when the compound was tested in a colon cancer xenograft mouse model. Additionally, the synergic antitumor effects of PsA and 5-FU on colon cancer cells were observed. Using annexin V and terminal deoxynucleotidyl transferase 2′-deoxyuridine 5′-triphosphate nick end labeling assays, it was demonstrated that levels of apoptosis induction in HT-29 cells treated with PsA or 5-FU were significantly increased compared with the untreated control cells (P<0.05). Western blot analyses were then performed, and the results revealed an increase in tumor protein 53 and cleaved caspase 9, and a decrease in B-cell lymphoma 2 protein expressions in PsA and PsA + 5-FU treated colon cancer cells compared with the vehicle-treated (PBS) cells. In summary, PsA exhibited anticancer activity in human colon cancer cells in vitro and in vivo, in isolation and synergistically with 5-FU, through apoptosis induction.
机译:结肠癌是消化系统恶性肿瘤的常见类型之一。一线化疗药物氟尿嘧啶(5-FU)对结肠癌的疗效由于疗效差和副作用大,在临床上仍然受到限制。在本研究中,从白头翁提取物中的活性化合物白头翁皂苷A(PsA)的抗癌活性被分离出来,并在体内和体外进行了检查。已证明PsA显着抑制人结肠癌HT-29细胞的生长。当在结肠癌异种移植小鼠模型中测试该化合物时,也观察到了这种抑制活性。另外,观察到PsA和5-FU对结肠癌细胞的协同抗肿瘤作用。使用膜联蛋白V和末端脱氧核苷酸转移酶2'-脱氧尿苷5'-三磷酸缺口末端标记测定法,表明与未处理的对照细胞相比,经PsA或5-FU处理的HT-29细胞的凋亡诱导水平显着增加( P <0.05)。然后进行蛋白质印迹分析,结果显示与载体载体相比,PsA和PsA + 5-FU处理的结肠癌细胞中肿瘤蛋白53的增加和caspase 9的裂解,B细胞淋巴瘤2蛋白的表达减少。处理过的(PBS)细胞。总而言之,PsA通过凋亡诱导在体外和体内在人类结肠癌细胞中表现出抗癌活性,与5-FU分离并协同作用。

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