Department of Obstetrics, Gynecology & Reproductive Sciences, Yale University School of Medicine, New Haven, CT, USA.
J Exp Clin Cancer Res. 2011 Nov 10;30(1):106. doi: 10.1186/1756-9966-30-106.
We evaluated the expression of human trophoblastic cell-surface marker (Trop-2) and the potential of hRS7 - a humanized monoclonal anti-Trop-2 antibody - as a therapeutic strategy against treatment-refractory human uterine (UMMT) and ovarian (OMMT) carcinosarcoma cell lines.
Trop-2 expression was evaluated by immunohistochemistry (IHC) in paraffin-embedded tumor tissues, by real-time polymerase-chain-reaction (RT-PCR) and flow-cytometry in cell lines. Sensitivity to hRS7 antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity was tested using 5-hour chromium-release assays against UMMT and OMMT cells.
Trop-2 expression was elevated in 9 of 26 (35%) UMMT and 8 of 14 (57%) OMMT tissues tested by IHC. Positivity for Trop-2 mRNA by RT-PCR and surface expression by flow cytometry were detected in 2 of 4 cell lines, with high positivity noted in OMMT-ARK-2. OMMT-ARK-2 was highly sensitive to hRS7 ADCC (range: 34.7-41.0%; P < 0.001) with negligible cytotoxicity seen in the absence of hRS7 or in the presence of control antibody (range: 1.1-2.5%). Human IgG did not significantly inhibit ADCC while human complement increased, hRS7-mediated-cytotoxicity against OMMT-ARK-2.
Trop-2 is overexpressed in a proportion of UMMT and OMMT, and hRS7 may represent a novel, potentially highly effective treatment option for patients with treatment-refractory carcinosarcomas overexpressing Trop-2.
我们评估了人滋养层细胞表面标志物(Trop-2)的表达以及 hRS7 的潜力——一种人源化单克隆抗 Trop-2 抗体——作为治疗难治性人子宫(UMMT)和卵巢(OMMT)癌肉瘤细胞系的治疗策略。
通过免疫组织化学(IHC)在石蜡包埋的肿瘤组织中评估 Trop-2 的表达,通过实时聚合酶链反应(RT-PCR)和细胞系中的流式细胞术进行评估。使用 5 小时铬释放测定法测试 hRS7 抗体依赖性细胞毒性(ADCC)和补体依赖性细胞毒性对 UMMT 和 OMMT 细胞的敏感性。
通过 IHC 测试,在 26 个 UMMT 组织中的 9 个(35%)和 14 个 OMMT 组织中的 8 个(57%)中升高了 Trop-2 表达。在 4 个细胞系中的 2 个中检测到 Trop-2 mRNA 的 RT-PCR 阳性和流式细胞术的表面表达,在 OMMT-ARK-2 中检测到高度阳性。OMMT-ARK-2 对 hRS7 ADCC 高度敏感(范围:34.7-41.0%;P < 0.001),在没有 hRS7 或存在对照抗体的情况下观察到可忽略不计的细胞毒性(范围:1.1-2.5%)。人 IgG 对 ADCC 没有显著抑制作用,而人补体增加了 hRS7 对 OMMT-ARK-2 的介导细胞毒性。
Trop-2 在一部分 UMMT 和 OMMT 中过度表达,hRS7 可能代表一种新的、潜在的高度有效的治疗选择,用于治疗过度表达 Trop-2 的治疗抵抗性癌肉瘤患者。