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Phospho-S6 ribosomal protein: a potential new predictive sarcoma marker for targeted mTOR therapy

机译:磷酸化S6核糖体蛋白:靶向mTOR治疗的潜在新的预测性肉瘤标志物

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Metastatic sarcomas are commonly resistant to chemotherapy. The serine/threonine kinase, mammalian target of rapamycin (mTOR), is a protein kinase of the phosphatidylinositol 3-kinase (PI3K)/AKT signaling pathway thought to have a key role in controlling cancer growth and thus is an important target for cancer therapy. Several inhibitors of mTOR are in clinical trials, including AP23573, which is being tested on metastatic sarcomas and other tumors. We hypothesized that a marker for the activity of mTOR, phosphorylated S6 ribosomal protein, would be predictive of clinical response to the drug, that is, high tumor expression would signify better response than low expression. This was a blinded study. Of 26 patients treated, 20 remained on study, with available paraffin blocks. Fourteen patients received AP23573 alone and six patients received AP23573 in combination with adriamycin. An antibody to the phosphorylated S6 ribosomal protein was used to stain the tumors, all high-grade sarcomas. Pretreatment biopsy or resection material was tested: the original tumor (n=6) or tumor recurrence/metastasis (n=14); either of these may have been after treatment with other agents. Staining was scored for both quantity/percentage of tumor cells and intensity. Scoring was performed without knowledge of tumor response. Staining quantity could be categorized into two natural groups: high expressors (≥20% of tumor cells, 11 cases) and low expressors (0–10% of tumor cells, 9 cases). The high-expression group had eight stable and three progressive cases (73% stable disease); the low-expression group had three stable and six progressive cases (67% progressive disease). Chi-square analysis showed statistical significance (P≤0.05) at this initial cutoff (10%) selected blindly. The level of phosphorylated S6 ribosomal protein expression was predictive of early tumor response to the mTOR inhibitor, suggesting that this is a promising new predictive sarcoma marker for targeted mTOR inhibitor therapy.
机译:转移性肉瘤通常对化疗耐药。丝氨酸/苏氨酸激酶是雷帕霉素(mTOR)的哺乳动物靶标,是磷脂酰肌醇3激酶(PI3K)/ AKT信号通路的蛋白激酶,被认为在控制癌症生长中起关键作用,因此是癌症治疗的重要靶标。多种mTOR抑制剂正在临床试验中,包括AP23573,该抑制剂正在转移性肉瘤和其他肿瘤中进行测试。我们假设,mTOR的活性标记磷酸化的S6核糖体蛋白可以预测对该药物的临床反应,即高肿瘤表达比低表达预示更好的反应。这是一项盲目的研究。在接受治疗的26例患者中,有20例仍在研究中,有可用的石蜡块。 14例患者单独接受AP23573,6例患者联合阿霉素联合接受AP23573。磷酸化的S6核糖体蛋白抗体被用于对所有高级肉瘤进行染色。测试了治疗前的活检或切除材料:原始肿瘤(n = 6)或肿瘤复发/转移(n = 14);这些中的任何一个都可能是在用其他药物治疗之后。对肿瘤细胞的数量/百分比和强度进行染色评分。在不了解肿瘤反应的情况下进行评分。染色量可分为两个自然类别:高表达者(占肿瘤细胞的≥20%,11例)和低表达者(占肿瘤细胞的0-10%,9例)。高表达组有8例稳定病例和3例进行性病例(疾病稳定率为73%);低表达组有3例稳定和6例进行性疾病(67%进行性疾病)。卡方分析显示,在盲选此初始截止值(10%)时具有统计学意义(P≤0.05)。磷酸化的S6核糖体蛋白表达水平可预测对mTOR抑制剂的早期肿瘤反应,这表明这是靶向mTOR抑制剂治疗的有希望的新预测肉瘤标记物。

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