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大蒜衍生化合物S-烯丙基巯基半胱氨酸(SAMC)对间变性甲状腺癌细胞系8305C(HPACC)具有活性。

Garlic-derived compound S-allylmercaptocysteine (SAMC) is active against anaplastic thyroid cancer cell line 8305C (HPACC).

作者信息

Liu Yuexin, Yan Jinyin, Han Xiaochen, Hu Wanning

机构信息

Department of Surgical Oncology, Affiliated Hospital of Hebei United University, Tangshan, Hebei, China.

Department of Surgical Oncology, Tangshan People's Hospital, Tangshan, Hebei, China.

出版信息

Technol Health Care. 2015;23 Suppl 1:S89-93. doi: 10.3233/thc-150936.

Abstract

BACKGROUND

Epidemiological and experimental carcinogenesis studies provide evidence that components of garlic have anticancer activity.

OBJECTIVE

In this study, the apoptotic effects of Garlic-derived compound S-allylmercaptocysteine (SAMC) were investigated in 8305C human anaplastic thyroid carcinoma cells.

METHODS

The cell line 8305C (HPACC) were treated with SAMC and the MTT assay, flow cytometry (FCM), electron microscope method were used to test cell cycle, inhibitory rate and morphologic changes respectively.

RESULTS

HPACC-8305C cells were suppressed after exposure to SAMC of 0.02 mg/ml, 0.06 mg/ml, and 0.1 mg/ml for 48 h. Compared with the control, the difference was significant (P< 0.05). SAMC could induce apoptosis of the cells in a dose-dependent and non-linear manner and increase the proportion of cells in the G2/M phase. Compared with the control, the difference was significant in terms of the percentage of cells in the G2/M phase (P< 0.05). After exposure to SAMC at 0.02 mg/ml for 24 hours, HPACC-8305C cells showed typical morphologic change.

CONCLUSIONS

SAMC inhibits the growth of HPACC-8305C cells by induction of apoptotic cell death and inhibit telomerase activity, which appears to account for its anti-cancer activity.

摘要

背景

流行病学和实验性致癌研究提供了证据表明大蒜成分具有抗癌活性。

目的

在本研究中,对大蒜衍生化合物S -烯丙基半胱氨酸(SAMC)在8305C人未分化甲状腺癌细胞中的凋亡作用进行了研究。

方法

用SAMC处理8305C(HPACC)细胞系,分别采用MTT法、流式细胞术(FCM)、电子显微镜法检测细胞周期、抑制率和形态学变化。

结果

用0.02 mg/ml、0.06 mg/ml和0.1 mg/ml的SAMC处理HPACC - 8305C细胞48小时后,细胞受到抑制。与对照组相比,差异有统计学意义(P < 0.05)。SAMC能以剂量依赖性和非线性方式诱导细胞凋亡,并增加G2/M期细胞比例。与对照组相比,G2/M期细胞百分比差异有统计学意义(P < 0.05)。用0.02 mg/ml的SAMC处理HPACC - 8305C细胞24小时后,细胞出现典型形态学变化。

结论

SAMC通过诱导凋亡性细胞死亡抑制HPACC - 8305C细胞生长并抑制端粒酶活性,这似乎是其抗癌活性的原因。

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