首页> 美国卫生研究院文献>iScience >CCL8 Promotes Postpartum Breast Cancer by Recruiting M2 Macrophages
【2h】

CCL8 Promotes Postpartum Breast Cancer by Recruiting M2 Macrophages

机译:CCL8通过募集M2巨噬细胞促进产后乳腺癌

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The microenvironment of postpartum mammary gland promotes tumor growth and metastasis in animal models and is linked to increased risk of breast cancer and poor disease outcome in patients. Our previous studies showed the involvement of the chemokine CCL8 in breast cancer metastasis through modulation of the tumor-promoting activity of the tumor microenvironment. Here we show that CCL8 is highly expressed during mammary gland involution and enhances the infiltration of M2 subtype macrophages at the second phase of involution. Cancer cell inoculation studies in Ccl8-deficient animals indicate that CCL8 accelerates tumor onset during involution but not in nulliparous animals. Depletion of macrophages abolished the tumor-promoting effect of CCL8 in involution suggesting the specific role of CCL8 in promoting tumor growth by recruiting macrophages. These results underscore the role of CCL8 in the development of postpartum breast cancer and suggest the potential value of targeting CCL8 in disease management.
机译:产后乳腺的微环境促进动物模型中的肿瘤生长和转移,与患者乳腺癌和疾病结果的风险增加有关。我们以前的研究表明,通过调节肿瘤微环境的肿瘤促进活性,表明趋化因子CCL8在乳腺癌转移中的参与。在这里,我们表明CCL8在乳腺下参与期间高度表达,并增强了M2亚型巨噬细胞的第二阶段的浸润。 CCL8缺乏动物中的癌细胞接种研究表明CCL8在阴部过程中加速肿瘤发作,但不含嵌入动物。巨噬细胞消除了CCL8的肿瘤促进作用,涉及CCL8通过募集巨噬细胞促进肿瘤生长的具体作用。这些结果强调了CCL8在产后乳腺癌发展中的作用,并提出了靶向CCL8在疾病管理中的潜在价值。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号