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首页> 外文期刊>Journal of Clinical Oncology >Novel staging protocol for non-small-cell lung cancers according to MRP-1/CD9 and KAI1/CD82 gene expression.
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Novel staging protocol for non-small-cell lung cancers according to MRP-1/CD9 and KAI1/CD82 gene expression.

机译:根据MRP-1 / CD9和KAI1 / CD82基因表达,用于非小细胞肺癌的新型分期方案。

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PURPOSE: The transmembrane-4 superfamily (TM4SF) is a recently discovered family of genes. Of the TM4SF members, MRP-1/CD9, KAI1/CD82, and ME491/CD63 have been reported to modulate tumor progression or metastasis. In this study, we investigated the relationships between these three genes, MRP-1, KAI1, and ME491, in patients with non-small-cell lung cancers (NSCLCs). Moreover, we assessed the prognostic value of evaluating the expressions of MRP-1, KAI1, and ME491 simultaneously in NSCLCs. PATIENTS AND METHODS: One hundred seventy-two patients up to stage IIIB NSCLC underwent radical surgery during the period of January 1991 through June 1994. Using a quantitative reverse-transcriptase polymerase chain reaction (RT-PCR) analysis, we studied the expression of MRP-1, KAI1, and ME491 genes in these patients. RESULTS: We found that 109 patients (63.4%) had MRP-1-positive tumors and 42 patients (24.4%) had KAl1-positive tumors. Conversely, all 172 patients expressed ME491. No relationship was found between MRP-1 expression and KAI1 expression. We classified these patients into three groups. The 36 patients who were positive for both MRP-1 and KAI1 were defined as group A; the 79 patients with reduced expression of either MRP-1 or KAI1 were defined as group B, and the remaining 57 patients with reduced expression of both MRP-1 and KAI1 were defined as group C. This new classification was correlated with nodal status, tumor status, and pathologic stage (P = .0056, P = .0003, and P < .0001, respectively). In NSCLC patients, the 5-year survival rate of group A patients was significantly better than that of group B patients and much better than that of group C patients (86.8%, 53.9%, and 31.5%, respectively; P < .0001). Cox multivariate regression analysis showed that this new classification in NSCLCs was a significant prognostic factor, as was the nodal status (P < .0001). CONCLUSION: Our results suggest that a low MRP-1 and KAI1 expression by tumors of the lung may be associated with poor prognosis. It is conceivable that the evaluation for MRP-1 and KAI1 expression may identify node-negative lung cancer patients who are at high risk for early disease recurrence, and thus need intensive adjuvant therapy.
机译:目的:跨膜4超家族(TM4SF)是最近发现的基因家族。在TM4SF成员中,据报道MRP-1 / CD9,KAI1 / CD82和ME491 / CD63调节肿瘤的进展或转移。在这项研究中,我们调查了非小细胞肺癌(NSCLC)患者这三个基因MRP-1,KAI1和ME491之间的关系。此外,我们评估了同时评估MCL-1,KAI1和ME491在NSCLC中的表达的预后价值。病人与方法:1991年1月至1994年6月,对IIIB期NSCLC的172例患者进行了根治性手术。我们使用定量逆转录酶聚合酶链反应(RT-PCR)分析了MRP的表达这些患者中的-1,KAI1和ME491基因。结果:我们发现109例(63.4%)患有MRP-1阳性肿瘤,42例(24.4%)患有KAl1阳性肿瘤。相反,所有172例患者均表达ME491。在MRP-1表达和KAI1表达之间未发现任何关系。我们将这些患者分为三组。将MRP-1和KAI1均为阳性的36例患者定义为A组。将MRP-1或KAI1表达降低的79例患者定义为B组,其余MRP-1和KAI1表达降低的57例患者定义为C组。这一新分类与淋巴结状态,肿瘤相关状态和病理分期(分别为P = .0056,P = .0003和P <.0001)。在NSCLC患者中,A组患者的5年生存率显着优于B组患者,并且远高于C组患者(分别为86.8%,53.9%和31.5%; P <.0001) 。 Cox多元回归分析表明,NSCLC中的这一新分类是重要的预后因素,淋巴结状态也是如此(P <.0001)。结论:我们的结果表明,肺肿瘤中MRP-1和KAI1的低表达可能与预后不良有关。可以想象,对MRP-1和KAI1表达的评估可以确定淋巴结阴性的肺癌患者,这些患者早期疾病复发的风险很高,因此需要强化辅助治疗。

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