Eid H, Géczi L, Bodrogi I, Institoris E, Bak M
National Institute of Oncology, Center of Pathology, Budapest, Hungary.
J Cancer Res Clin Oncol. 1998 Jan;124(1):31-6. doi: 10.1007/s004320050130.
Data on the involvement of elevated metallothionein (MT) expression in resistance to some of the commonly used anticancer treatments are scattered and conflicting. This encouraged us to examine further the contribution of metallothionein expression to the development of this resistance phenotype.
Formalin-fixed, paraffin-embedded blocks of primary untreated germ cell testicular tumor specimens, obtained from 77 patients following radical orchiectomy, were examined for their MT expression using monoclonal antibody and immunohistochemistry. Clinical staging, the chemotherapeutic schedule and evaluation of response to treatment (defining objective response) were performed according to UICC criteria.
All tumor types, including seminomas and nonseminomas, expressed MT, regardless of their histology and clinical stage. The immunoreactivity of MT showed a significant positive correlation with the clinical sensitivity of cancer to antitumor therapy (P = 0.0001).
In patients with germ cell testicular tumors, high MT expression, as detected by immunohistochemistry, predicts a better response rate to chemotherapy whereas tumors lacking or demonstrating low MT expression show a worse prognosis. These data do not support the hypothesis that MT overexpression contributes to cisplatinum resistance, at least in this tumor type.
关于金属硫蛋白(MT)表达升高与某些常用抗癌治疗耐药性之间关系的数据零散且相互矛盾。这促使我们进一步研究金属硫蛋白表达对这种耐药表型发展的作用。
对77例患者根治性睾丸切除术后获得的原发性未治疗生殖细胞睾丸肿瘤标本的福尔马林固定、石蜡包埋块,使用单克隆抗体和免疫组织化学检测其MT表达。根据国际抗癌联盟(UICC)标准进行临床分期、化疗方案及治疗反应评估(定义客观反应)。
所有肿瘤类型,包括精原细胞瘤和非精原细胞瘤,无论其组织学类型和临床分期如何,均表达MT。MT的免疫反应性与癌症对抗肿瘤治疗的临床敏感性呈显著正相关(P = 0.0001)。
在生殖细胞睾丸肿瘤患者中,免疫组织化学检测到的高MT表达预示着对化疗有更好的反应率,而缺乏或显示低MT表达的肿瘤预后较差。这些数据不支持MT过表达导致顺铂耐药的假说,至少在这种肿瘤类型中如此。