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首页> 外文期刊>Human Pathology >Lower expression levels of the transforming growth factor beta receptor type II protein are associated with a less aggressive tumor phenotype and improved survival among patients with clear cell renal cell carcinoma.
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Lower expression levels of the transforming growth factor beta receptor type II protein are associated with a less aggressive tumor phenotype and improved survival among patients with clear cell renal cell carcinoma.

机译:转化生长因子β受体II型蛋白的较低表达水平与侵袭性较低的肿瘤表型和透明细胞肾细胞癌患者的生存期改善有关。

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Loss of expression of the transforming growth factor beta type II receptor (TbetaRII) has been implicated as an important event in renal carcinogenesis; however, its role as a potential prognostic factor remains poorly understood. Using archived tumor samples and long-term follow-up on a cohort of 280 clear cell renal cell carcinoma (ccRCC) patients treated with surgery from 1980 to 1998, we evaluated the association of TbetaRII expression and cancer-specific survival in both a univariate and multivariate setting. Low tumor expression of TbetaRII is associated with a less aggressive tumor phenotype at time of surgery. Moreover, those patients with lower levels of TbetaRII expression experience better cancer-specific survival than patients with higher levels of TbetaRII expression (log rank P = .034). Based on a Cox proportional hazard model adjusting for age, patients with tumors showing low (hazard ratio, 0.49; 95% confidence interval, 0.27-0.88) and moderate (hazard ratio, 0.7; 95% confidence interval, 0.40-1.23) TbetaRII expression are at decreased risk of RCC death compared with patients with tumors having high levels of TbetaRII expression. Adjustment for well-known pathologic predictors of RCC outcome attenuates the association of TbetaRII expression and ccRCC survival. Of interest, the association with TbetaRII expression appears more pronounced among those patients with tumors showing less aggressive phenotypes. Data from this investigation are the first to suggest that loss of TbetaRII expression is associated with improved ccRCC patient survival, especially among those patients with less aggressive disease profiles at time of surgery.
机译:转化生长因子βII型受体(TbetaRII)的表达丧失被认为是肾癌发生中的重要事件;然而,其作为潜在预后因素的作用仍知之甚少。使用存档的肿瘤样本并对1980年至1998年接受手术治疗的280例透明细胞肾细胞癌(ccRCC)患者进行长期随访,我们评估了单变量和随机变量中TbetaRII表达与癌症特异性生存的关系。多变量设置。 TbetaRII的低肿瘤表达与手术时侵袭性较小的肿瘤表型有关。而且,那些具有较低水平的TbetaRII表达的患者比具有较高水平的TbetaRII表达的患者具有更好的癌症特异性生存率(对数秩P = .034)。基于针对年龄调整的Cox比例风险模型,肿瘤患者的TbetaRII表达较低(风险比为0.49; 95%置信区间为0.27-0.88),中等(风险比为0.7; 95%置信区间为0.40-1.23)与具有高水平TbetaRII表达的肿瘤患者相比,这些患者的RCC死亡风险降低。对RCC结局的著名病理预测因子的调整会减弱TbetaRII表达与ccRCC存活率的关联。有趣的是,在那些表现出较少侵袭性表型的肿瘤患者中,与TbetaRII表达的关联更为明显。这项研究的数据首次表明,TbetaRII表达的丧失与ccRCC患者的存活率提高有关,尤其是在那些手术时病情较轻的患者中。

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