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首页> 外文期刊>Saudi Journal of Biological Sciences >Anticancer and immunomodulatory effect of rhaponticin on Benzo(a)Pyrene-induced lung carcinogenesis and induction of apoptosis in A549 cells
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Anticancer and immunomodulatory effect of rhaponticin on Benzo(a)Pyrene-induced lung carcinogenesis and induction of apoptosis in A549 cells

机译:逆南菌素对苯并(A)芘诱导的肺癌发生和A549细胞凋亡的抗癌和免疫调节作用

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In worldwide, one of the most important cancer-related death is lung cancer. Also has the highest mortality rate between various cancer types. The count of lung cancer occurrence is increasing with an increased frequency by smoking. Proficient chemoprevention approaches are needed to prevent the occurrence of lung cancer. Therefore, the aim of this exploration is to determine the therapeutic impact on the immune modulatory effect of rhaponticin on lung tumorigenesis in vivo and in vitro cytotoxicity effect in A549 cells of human lung cancer. Lung cancer tumorigenesis in mice was challenged with benzo(a)pyrene (BaP) with 50?mg/kg bodyweight (b.wt) as oral administration for 6?weeks (two times/week). Rhaponticin were given orally 30?mg/kg b.wt (two times/week) in BaP induced mice from 12?weeks to 18?weeks. After treatment completes, the body weight was measured and then blood, lung tissue was collected for various parameters detection. The results evidenced that BaP induced mice decreased the bodyweight, increased lung weight, increased tumor markers (AHH, CEA and LDH), and increased the proinflammatory cytokines. The enzyme catalase, superoxide dismutase activity was decreased and increased lipid peroxidation in immune comprising cells compared with the control cells. Moreover, rhaponticin treatment improves in chemical assays and also the histopathological alteration of lung tissues. The present findings provide evidence about the therapeutic potentials of rhaponticin against BaP triggered lung tumorigenesis.
机译:在全球范围内,最重要的癌症死亡之一是肺癌。在各种癌症类型之间也具有最高的死亡率。肺癌发生的计数随着吸烟的频率增加而增加。需要精通化学普化方法来防止肺癌发生。因此,该探索的目的是确定对人肺癌A549细胞体内肺肿瘤内肺肿瘤性肺肿瘤鉴定的治疗影响。小鼠中的肺癌肿瘤发生症是用50μmmg/ kg体重(b.wt)的苯并(a)芘(bap)攻击6?周(两次/周)。 rhaponticin在12?周至18〜18岁的Bap诱导小鼠中口服30?mg / kg b.wt(两次/ kg b.wt(两次/周)。治疗完成后,测量体重然后血液,收集肺组织以进行各种参数检测。结果证明,BAP诱导小鼠减少了体重,肺重量增加,肿瘤标志物增加(AHH,CEA和LDH),并增加了促炎细胞因子。与对照细胞相比,酶过氧化酶,超氧化物歧化酶活性降低并增加了免疫细胞中的脂质过氧化。此外,湿法蛋白治疗改善了化学测定和肺组织的组织病理学改变。目前的研究结果提供了有关湿法蛋白对Bap触发肺肿瘤瘤的治疗潜力的证据。

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