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肝母细胞瘤患者中的血小板生成素

Thrombopoietin in patients with hepatoblastoma.

作者信息

Komura E, Matsumura T, Kato T, Tahara T, Tsunoda Y, Sawada T

机构信息

Department of Pediatrics, Kyoto Prefectural University of Medicine, Japan.

出版信息

Stem Cells. 1998;16(5):329-33. doi: 10.1002/stem.160329.

Abstract

Marked thrombocytosis (over 50 x 10(4)/microl) is frequently seen in patients with hepatoblastoma. Thrombopoietin (TPO), c-mpl ligand, has recently been purified as the major physiological regulator of the thrombopoiesis and is mainly produced in the liver. Since it is possible that TPO participates in thrombocytosis and the tumor growth of this particular hepatic tumor, serum TPO levels in addition to interleukin 1beta (IL-1beta) and IL-6 levels were assessed in seven untreated patients by using a sandwich enzyme-linked immunosorbent assay. High serum TPO levels were observed in all of the examined patients. The level ranged from 3.15 to 11.02 (mean +/- standard deviation; 6.08+/-1.25) fmol/ml. IL-6 levels were also somewhat higher than normal. Platelet counts, however, appeared to correlate more with serum TPO levels (p = 0.1) than with IL-1beta (p = 0.5) and IL-6 (p = 0.2) levels. Furthermore, using the reverse transcriptase polymerase chain reaction method, the expression of c-mpl mRNA was found in five of eight hepatoblastoma tissues as well as TPO mRNA in all eight tissues. These observations suggest that thrombocytosis in hepatoblastoma patients results from the production of cytokine members, including TPO, within tumor tissues. Additionally, it is possible that TPO might act as a type of autocrine and/or paracrine system for cellular growth in this tumor.

摘要

在肝母细胞瘤患者中经常可见显著的血小板增多症(超过50×10⁴/微升)。血小板生成素(TPO),即c-mpl配体,最近已被纯化,是血小板生成的主要生理调节因子,主要在肝脏中产生。由于TPO可能参与这种特定肝脏肿瘤的血小板增多症和肿瘤生长,因此通过夹心酶联免疫吸附测定法评估了7例未经治疗患者的血清TPO水平以及白细胞介素1β(IL-1β)和IL-6水平。在所有检查的患者中均观察到高血清TPO水平。该水平范围为3.15至11.02(平均值±标准差;6.08±1.25)飞摩尔/毫升。IL-6水平也略高于正常水平。然而,血小板计数似乎与血清TPO水平(p = 0.1)的相关性比与IL-1β(p = 0.5)和IL-6(p = 0.2)水平的相关性更大。此外,使用逆转录酶聚合酶链反应方法,在8个肝母细胞瘤组织中的5个中发现了c-mpl mRNA的表达,并且在所有8个组织中均发现了TPO mRNA的表达。这些观察结果表明,肝母细胞瘤患者的血小板增多症是由肿瘤组织内包括TPO在内的细胞因子成员的产生所致。此外,TPO有可能作为该肿瘤细胞生长的一种自分泌和/或旁分泌系统。

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