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真性红细胞增多症-1基因在原发性血小板增多症中的过表达。

Overexpression of the polycythemia rubra vera-1 gene in essential thrombocythemia.

作者信息

Teofili Luciana, Martini Maurizio, Luongo Myriam, Di Mario Antonella, Leone Giuseppe, De Stefano Valerio, Larocca Luigi Maria

机构信息

Istituto di Ematologia and Istituto di Anatomia Patologica, Università Cattolica del Sacro Cuore, Rome, Italy.

出版信息

J Clin Oncol. 2002 Oct 15;20(20):4249-54. doi: 10.1200/JCO.2002.11.507.

Abstract

PURPOSE

To examine the utility of polycythemia rubra vera-1 (PRV-1)-specific reverse transcriptase polymerase chain reaction (RT-PCR) to discriminate essential thrombocythemia (ET) and polycythemia vera (PV) from secondary thrombocytosis (ST) or secondary erythrocytosis (SE).

PATIENTS AND METHODS

We analyzed the expression of PRV-1 in granulocytes isolated from 37 patients with ET, 37 patients with PV, 25 patients with ST, 10 patients with SE, 25 patients with secondary leukocytosis (SL), five patients with chronic myelogenous leukemia (CML), five patients with chronic idiopathic myelofibrosis (IM), five patients with myelodysplastic syndrome (MDS), and 20 normal individuals by PRV-1-specific RT-PCR. In female patients, PRV-1 expression was correlated with clonality analysis as assessed by the human androgen receptor polymorphism assay.

RESULTS

PRV-1 was not expressed in granulocytes isolated from normal individuals or from patients with ST, SE, CML, IM, MDS, and inflammatory/infectious SL. On the contrary, all ET patients, 35 of 37 PV patients, and five patients with acute postsurgery and posttraumatic SL overexpressed PRV-1. All the cases with monoclonal hematopoiesis (17 of 21 with ET and 12 of 12 with PV) expressed PRV-1, yet PRV-1 overexpression extended also over the cases of ET showing polyclonal hematopoiesis (four of 20).

CONCLUSION

The overexpression of PRV-1 seems to be a useful tool for discriminating ET and PV from ST and SE, thus offering an innovative diagnostic approach on the basis of the detection of positive diagnostic criteria instead of exclusion criteria.

摘要

目的

探讨真性红细胞增多症-1(PRV-1)特异性逆转录聚合酶链反应(RT-PCR)在鉴别原发性血小板增多症(ET)、真性红细胞增多症(PV)与继发性血小板增多症(ST)或继发性红细胞增多症(SE)中的应用价值。

患者与方法

我们通过PRV-1特异性RT-PCR分析了37例ET患者、37例PV患者、25例ST患者、10例SE患者、25例继发性白细胞增多症(SL)患者、5例慢性粒细胞白血病(CML)患者、5例慢性特发性骨髓纤维化(IM)患者、5例骨髓增生异常综合征(MDS)患者及20名正常个体分离的粒细胞中PRV-1的表达情况。在女性患者中,PRV-1表达与通过人类雄激素受体多态性检测评估的克隆性分析相关。

结果

正常个体或ST、SE、CML、IM、MDS患者及炎症/感染性SL患者分离的粒细胞中未检测到PRV-1表达。相反,所有ET患者、37例PV患者中的35例以及5例急性术后和创伤后SL患者PRV-1均过度表达。所有单克隆造血的病例(ET患者中的21例有17例,PV患者中的12例有12例)均表达PRV-1,但PRV-1过度表达也见于显示多克隆造血的ET病例(20例中有4例)。

结论

PRV-1的过度表达似乎是鉴别ET和PV与ST和SE的有用工具,从而基于检测阳性诊断标准而非排除标准提供一种创新的诊断方法。

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