Department of Pediatrics, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX 79905, USA.
Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX 79905, USA.
Molecules. 2018 Apr 14;23(4):905. doi: 10.3390/molecules23040905.
Increasing evidence suggests that dietary carotenoids may reduce the risk of breast cancer. However, anti-breast cancer effects of carotenoids have been controversial, albeit understudied. Here, we investigated the effects of specific carotenoids on a wide range of breast cancer cell lines, and found that among several carotenoids (including β-carotene, lutein, and astaxanthin), lutein significantly inhibits breast cancer cell growth by inducing cell-cycle arrest and caspase-independent cell death, but it has little effect on the growth of primary mammary epithelial cells (PmECs). Moreover, lutein-mediated growth inhibition of breast cancer cells is quantitatively similar to that induced by chemotherapeutic taxanes, paclitaxel and docetaxel, and exposure to lutein plus taxanes additively inhibits breast cancer cell growth. Analysis of mechanisms showed that lutein treatment significantly increases the intracellular reactive oxygen species (ROS) production in triple-negative breast cancer (TNBC) cells, but not in normal PmECs. Lutein-induced growth inhibition is also attenuated by the radical oxygen scavenger -acetyl cysteine, suggesting a role for ROS generation in the growth inhibitory effect of lutein on TNBC cells. Additionally, we found that the p53 signaling pathway is activated and HSP60 levels are increased by lutein treatment, which may contribute partly to the induction of growth inhibition in TNBC cells. Our findings show that lutein promotes growth inhibition of breast cancer cells through increased cell type-specific ROS generation and alternation of several signaling pathways. Dietary lutein supplementation may be a promising alternative and/or adjunct therapeutic candidate against breast cancer.
越来越多的证据表明,膳食类胡萝卜素可能降低乳腺癌的风险。然而,类胡萝卜素的抗癌作用一直存在争议,尽管研究还不够充分。在这里,我们研究了特定类胡萝卜素对多种乳腺癌细胞系的影响,发现几种类胡萝卜素(包括β-胡萝卜素、叶黄素和虾青素)中,叶黄素通过诱导细胞周期停滞和半胱天冬酶非依赖性细胞死亡显著抑制乳腺癌细胞生长,但对原代乳腺上皮细胞(PmECs)的生长几乎没有影响。此外,叶黄素介导的乳腺癌细胞生长抑制与化疗紫杉烷类药物紫杉醇和多西他赛诱导的生长抑制具有定量相似性,并且暴露于叶黄素加紫杉烷类药物可协同抑制乳腺癌细胞生长。机制分析表明,叶黄素处理可显著增加三阴性乳腺癌(TNBC)细胞中的细胞内活性氧(ROS)产生,但对正常 PmECs 没有影响。叶黄素诱导的生长抑制也被自由基清除剂 -乙酰半胱氨酸减弱,表明 ROS 生成在叶黄素对 TNBC 细胞生长抑制作用中的作用。此外,我们发现叶黄素处理可激活 p53 信号通路并增加 HSP60 水平,这可能部分有助于诱导 TNBC 细胞的生长抑制。我们的研究结果表明,叶黄素通过增加细胞类型特异性 ROS 生成和改变几种信号通路来促进乳腺癌细胞的生长抑制。膳食叶黄素补充可能是一种有前途的替代和/或联合治疗乳腺癌的候选药物。