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Anticancer effects of fucoxanthin and fucoxanthinol on colorectal cancer cell lines and colorectal cancer tissues

机译:岩藻黄质和岩藻黄质对大肠癌细胞系和大肠癌组织的抗癌作用

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摘要

Colorectal cancer is one of the most malignant neoplasms worldwide. Fucoxanthin is a carotenoid present in the chloroplasts of brown seaweeds. In the present study, the anticancer effects of fucoxanthin and its metabolite, fucoxanthinol, on 6 colorectal cancer cell lines and 20 tissue samples from surgically resected clinical colorectal cancer specimens were examined using a collagen-gel droplet embedded culture drug sensitivity test (CD-DST). The in vitro sensitivity to fucoxanthin, fucoxanthinol and the anticancer drugs is expressed as T/C (%), where T is the absorbance of cells which stained by neutral red treated with carotenoids and C is the absorbance of non-staining cells. Fucoxanthin and fucoxanthinol decreased the T/C (%) of Caco-2, WiDr, HCT116, and DLD-1 cell lines at doses of 20 µM. Fucoxanthinol also decreased the T/C (%) of SW620 cells, while the T/C (%) of Colo205 cells was not reduced by treatment with either carotenoid. Specifically, the T/C (%) of Caco-2 and WiDr cells, which were incubated in carotenoid-free medium for 6 days following treatment with 20 µM fucoxanthinol for 24 h, was markedly decreased to 1.4±0.2 and 12.0±0.3%, respectively. Furthermore, fucoxanthin and fucoxanthinol decreased the T/C (%) in colorectal cancer tissue samples. Notably, 20 µM fucoxanthinol treatment resulted in a higher proportion of colorectal cancer samples with a T/C (%) of <50% (13/20, 65%) compared with samples treated with 20 µM fucoxanthin (2/20, 10%). The median T/C (%) value of 35.1% for the 20 cancers specimens treated with 20 µM fucoxanthinol was lower than the median T/C (%) values of 86.3% and 75.8% for those treated with fluorouracil and paclitaxel, respectively. These results suggested that fucoxanthin and fucoxanthinol may be of use as chemotherapeutic agents in colorectal cancer.
机译:大肠癌是世界上最恶性的肿瘤之一。岩藻黄质是类胡萝卜素,存在于褐藻的叶绿体中。在本研究中,使用胶原蛋白凝胶液滴包埋培养药物敏感性试验(CD-DST)研究了岩藻黄质及其代谢产物岩藻黄质对6种结直肠癌细胞系和20例手术切除的临床结直肠癌标本的组织样本的抗癌作用。 )。体外对岩藻黄质,岩藻黄质和抗癌药物的敏感性表示为T / C(%),其中T是用类胡萝卜素处理的中性红染色的细胞的吸光度,C是非染色细胞的吸光度。岩藻黄质和岩藻黄质醇以20 µM的剂量降低了Caco-2,WiDr,HCT116和DLD-1细胞系的T / C(%)。岩藻黄酮还降低了SW620细胞的T / C(%),而通过两种类胡萝卜素处理均未降低Colo205细胞的T / C(%)。具体来说,将Caco-2和WiDr细胞的T / C(%)在用20 µM岩藻黄嘌呤处理24小时后在无类胡萝卜素的培养基中孵育6天后,显着降低至1.4±0.2和12.0±0.3% , 分别。此外,岩藻黄质和岩藻黄质降低了大肠癌组织样本中的T / C(%)。值得注意的是,与用20 µM岩藻黄质(2 / 20、10%)处理的样品相比,用20 µM岩藻黄质处理可导致更高的大肠癌样本,其T / C(%)<50%(13/20,65%)。 )。用20 µM岩藻黄嘌呤治疗的20个癌标本的T / C(%)中值(%)分别低于用氟尿嘧啶和紫杉醇治疗的20个癌症样品的T / C(%)中值(86.3%)和75.8%。这些结果表明,岩藻黄质和岩藻黄质可以用作结直肠癌的化学治疗剂。

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