Department of Biochemistry, Tufts University School of Medicine, Boston, Massachusetts, United States of America.
PLoS One. 2013 Sep 11;8(9):e73464. doi: 10.1371/journal.pone.0073464. eCollection 2013.
Inflammatory Breast Cancer (IBC) is a highly aggressive form of cancer characterized by high rates of proliferation, lymphangiogenesis and metastasis, and an overall poor survival. As regular green tea consumption has been associated with improved prognosis of breast cancer patients, including decreased risk of recurrence, here the effects of the green tea polyphenol epigallocatechin-3-gallate (EGCG) were tested on two IBC lines: SUM-149 and SUM-190. EGCG decreased expression of genes that promote proliferation, migration, invasion, and survival. Consistently, growth, invasive properties, and survival of IBC cells were reduced by EGCG treatment. EGCG also reduced lymphangiogenesis-promoting genes, in particular VEGF-D. Conditioned media from EGCG-treated IBC cells displayed decreased VEGF-D secretion and reduced ability to promote lymphangiogenesis in vitro as measured by hTERT-HDLEC lymphatic endothelial cell migration and tube formation. Tumorsphere formation by SUM-149 cells was robustly inhibited by EGCG, suggesting effects on self-renewal ability. Stem-like SUM-149 cells with high aldehyde dehydrogenase (ALDH) activity, previously implicated in poor patient prognosis, were isolated. EGCG treatment reduced growth and induced apoptosis of the stem-like SUM-149 cells in culture. In an orthotopic mouse model, EGCG decreased growth of pre-existing tumors derived from ALDH-positive stem-like SUM-149 cells and their expression of VEGF-D, which correlated with a significant decrease in peritumoral lymphatic vessel density. Thus, EGCG inhibits the overall aggressive IBC phenotype. Reduction of the stem-like cell compartment by EGCG may explain the decreased risk of breast cancer recurrence among green tea drinkers. Recent clinical trials demonstrate the efficacy of green tea polyphenol extracts in treatment of prostate cancer and lymphocytic leukemia with low toxicity. Given the poor prognosis of IBC patients, our findings suggest further exploration of EGCG or green tea in combinatorial treatments against active IBC disease or in maintenance regimens to avoid recurrence is warranted.
炎性乳腺癌 (IBC) 是一种侵袭性很强的癌症,其特征是增殖率高、淋巴管生成和转移率高,总体生存率低。由于经常饮用绿茶与改善乳腺癌患者的预后有关,包括降低复发风险,因此在这里测试了绿茶多酚表没食子儿茶素没食子酸酯 (EGCG) 对两种 IBC 细胞系:SUM-149 和 SUM-190 的影响。EGCG 降低了促进增殖、迁移、侵袭和存活的基因的表达。一致地,EGCG 处理降低了 IBC 细胞的生长、侵袭特性和存活。EGCG 还降低了淋巴管生成促进基因,特别是 VEGF-D。用 EGCG 处理的 IBC 细胞的条件培养基显示出 VEGF-D 分泌减少,并且体外淋巴管生成促进能力降低,如 hTERT-HDLEC 淋巴管内皮细胞迁移和管形成所测量的。SUM-149 细胞的肿瘤球形成被 EGCG 强烈抑制,表明对自我更新能力的影响。先前与患者预后不良相关的具有高醛脱氢酶 (ALDH) 活性的 SUM-149 细胞的干细胞样细胞被分离。EGCG 处理降低了培养物中干细胞样 SUM-149 细胞的生长并诱导其凋亡。在原位小鼠模型中,EGCG 降低了源自 ALDH 阳性干细胞样 SUM-149 细胞的现有肿瘤的生长及其 VEGF-D 的表达,这与肿瘤周围淋巴管密度的显著降低相关。因此,EGCG 抑制了整体侵袭性 IBC 表型。EGCG 减少干细胞样细胞群可能解释了绿茶饮用者乳腺癌复发风险降低的原因。最近的临床试验表明,绿茶多酚提取物在治疗前列腺癌和淋巴细胞白血病方面具有疗效,且毒性低。鉴于 IBC 患者的预后较差,我们的发现表明进一步探索 EGCG 或绿茶在针对活跃 IBC 疾病的联合治疗或在维持方案中以避免复发是合理的。