芹菜素在MMTV-PyMT自发乳腺癌小鼠肿瘤生长和肺转移中的作用

Effect of apigenin on spontaneous breast cancer growth and pulmonary metastasis in MMTV-PyMT and its mechanism

  • 摘要:
    目的 研究芹菜素对自发乳腺癌多瘤病毒中间T抗原小鼠(MMTV-PyMT)乳腺癌生长及肺转移的作用和机制。
    方法 使用9周龄的MMTV-PyMT雌性小鼠,芹菜素治疗组(n = 5)予腹腔注射芹菜素5 mg/kg,对照组 (n =5)予腹腔注射二甲基亚砜,共4周,治疗期间测量小鼠的体质量及肿瘤体积。4周后分离小鼠的肿瘤及肺组织,测量肿瘤的质量及计数肺表面结节。免疫组织化学染色检测肿瘤内增殖细胞和微血管的数目。
    结果 与对照组相比,芹菜素治疗组治疗4周后小鼠的肿瘤体积小于对照组,肿瘤质量轻于对照组,且芹菜素治疗组小鼠肺表面转移结节数目少于对照组(均P < 0.05)。免疫组织化学结果显示,芹菜素治疗组肿瘤内细胞增殖指数Ki67和微血管密度均低于对照组(均P < 0.05)。
    结论 芹菜素可能通过抑制肿瘤细胞增殖和血管生成来抑制MMTV-PyMT小鼠乳腺癌的生长和肺转移。

     

    Abstract:
    Objective To evaluate the effect of apigenin on breast cancer growth and lung metastasis in MMTV-PyMT.
    Methods MMTV-PyMT female mice aged 9-week were selected and divided into the apigenin treatment and control groups. In the apigenin treatment group (n = 5), mice were treated with intraperitoneal injection of 5 mg/kg apigenin, while those in the control group (n = 5) were given with intraperitoneal injection of DMSO at the equivalent dose for 4 weeks. Body weight and tumor volume of the mice were measured during the treatment. After 4 weeks, the tumors and lung tissues of the mice were isolated. Tumor weight was measured, and the number of nodules on the lung surface was counted. Immunohistochemical staining was used to detect the number of proliferating cells and microvessels in the tumor tissues.
    Results Compared with the control group, the tumor volume of the apigenin-treated mice was significantly smaller and tumor weight was significantly lighter than than those in the control group. Moreover, the number of metastatic nodules on the lung surface in the apigenin treatment group was significantly lower than that in the control group (all P < 0.05). The results of immunohistochemistry showed that the number of proliferating cells (Ki67) and microvessel density in the apigenin treatment group were significantly lower than those in the control group (both P < 0.05).
    Conclusion Apigenin significantly inhibits the growth and lung metastasis of breast cancer in MMTV-PyMT mice probably by inhibiting tumor cell proliferation and angiogenesis.

     

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