Department of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Department of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden; Department of Clinical Pathology/Cytology, Karolinska University Hospital, 17177 Stockholm, Sweden.
Cancer Lett. 2015 Oct 10;367(1):76-87. doi: 10.1016/j.canlet.2015.07.017. Epub 2015 Jul 21.
Breast cancer cells with stem cell characteristics (CSC) are a distinct cell population with phenotypic similarities to mammary stem cells. CSCs are important drivers of tumorigenesis and the metastatic process. Tamoxifen is the most widely used hormonal therapy for estrogen receptor (ER) positive cancers. In our study, tamoxifen was effective in reducing proliferation of ER + adherent cancer cells, but not their CSC population. We isolated, expanded and incubated CSC from seven breast cancers with or without tamoxifen. By genome-wide transcriptional analysis we identified tamoxifen-induced transcriptional pathways associated with ribosomal biogenesis and mRNA translation, both regulated by the mTOR-pathway. We observed induction of the key mTOR downstream targets S6K1, S6RP and 4E-BP1 in-patient derived CSCs by tamoxifen on protein level. Using the mTOR inhibitors rapamycin, everolimus and PF-04691502 (a dual PI3K/mTOR inhibitor) and in combination with tamoxifen, significant reduction in mammosphere formation was observed. Hence, we suggest that the CSC population play a significant role during endocrine resistance through activity of the mTOR pathway. In addition, tamoxifen further stimulates the mTOR-pathway but can be antagonized using mTOR-inhibitors.
具有干细胞特征的乳腺癌细胞(CSC)是一种具有与乳腺干细胞相似表型的独特细胞群体。CSC 是肿瘤发生和转移过程的重要驱动因素。他莫昔芬是最广泛用于治疗雌激素受体(ER)阳性癌症的激素治疗药物。在我们的研究中,他莫昔芬有效抑制了 ER+黏附癌细胞的增殖,但对其 CSC 群体无效。我们从 7 例乳腺癌中分离、扩增和培养了 CSC,无论是否使用他莫昔芬。通过全基因组转录分析,我们确定了与核糖体生物发生和 mRNA 翻译相关的他莫昔芬诱导的转录途径,这些途径均受 mTOR 途径调节。我们观察到他莫昔芬在蛋白水平上诱导了患者来源的 CSC 中关键的 mTOR 下游靶标 S6K1、S6RP 和 4E-BP1 的表达。使用 mTOR 抑制剂雷帕霉素、依维莫司和 PF-04691502(一种双重 PI3K/mTOR 抑制剂)以及与他莫昔芬联合使用,观察到类乳腺球体形成显著减少。因此,我们认为 CSC 群体通过 mTOR 途径的活性在内分泌抵抗期间发挥重要作用。此外,他莫昔芬进一步刺激 mTOR 途径,但可以使用 mTOR 抑制剂拮抗。