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前列腺癌和神经内分泌肿瘤中的血浆嗜铬粒蛋白A

Plasma chromogranin A in prostatic carcinoma and neuroendocrine tumors.

作者信息

Kimura N, Hoshi S, Takahashi M, Takeha S, Shizawa S, Nagura H

机构信息

Department of Pathology, Tohoku University School of Medicine, Japan.

出版信息

J Urol. 1997 Feb;157(2):565-8.

PMID:8996358
Abstract

PURPOSE

Chromogranin A is a good tumor marker for neuroendocrine cells. Whether plasma chromogranin A could be a useful marker for neuroendocrine differentiation of prostatic carcinoma and neuroendocrine tumors was investigated using an enzyme-linked immunosorbent assay.

MATERIALS AND METHODS

Plasma levels of chromogranin A were measured by enzyme-linked immunosorbent assay in 33 patients with prostatic carcinoma, 10 with benign prostatic hyperplasia (BPH) and 13 with neuroendocrine tumors (2 medullary thyroid carcinomas, 1 thymic carcinoid, 1 gastrin producing duodenal carcinoid, 3 nonfunctioning pancreatic endocrine tumors, 2 neuroblastomas, 3 pheochromocytomas and 1 carotid body tumor).

RESULTS

The normal level of chromogranin A from 40 healthy volunteers was 30 +/- 11 units per 1. (mean plus or minus standard deviation). Mean plasma chromogranin A in patients with BPH and prostatic carcinoma was 52.4 +/- 12.9 and 67.5 +/- 22.9 units per 1., respectively. All patients with neuroendocrine tumors, except 1 with a nonfunctioning pancreatic endocrine tumor, had elevated chromogranin A (mean 401 +/- 409 units per 1.). There were significant differences in plasma chromogranin A level between patients with BPH and neuroendocrine tumors (p < 0.01), prostatic carcinoma and neuroendocrine tumors (p < 0.01), and BPH and prostatic carcinoma (p < 0.05). Of the 33 patients with prostatic carcinoma 5 had elevated chromogranin A, only 1 of whom had elevated prostate specific antigen.

CONCLUSIONS

Chromogranin A is an excellent marker for neuroendocrine tumors, particularly nonfunctioning tumors, and measurement of chromogranin A is also useful to detect prostatic carcinoma in patients whose prostate specific antigen is not elevated.

摘要

目的

嗜铬粒蛋白A是神经内分泌细胞的一种良好肿瘤标志物。本研究采用酶联免疫吸附测定法,探讨血浆嗜铬粒蛋白A是否可作为前列腺癌和神经内分泌肿瘤神经内分泌分化的有用标志物。

材料与方法

采用酶联免疫吸附测定法检测33例前列腺癌患者、10例良性前列腺增生(BPH)患者和13例神经内分泌肿瘤患者(2例甲状腺髓样癌、1例胸腺类癌、1例产生胃泌素的十二指肠类癌、3例无功能胰腺内分泌肿瘤、2例神经母细胞瘤、3例嗜铬细胞瘤和1例颈动脉体瘤)的血浆嗜铬粒蛋白A水平。

结果

40名健康志愿者的嗜铬粒蛋白A正常水平为每1单位30±11(均值±标准差)。BPH患者和前列腺癌患者的血浆嗜铬粒蛋白A均值分别为每1单位52.4±12.9和67.5±22.9。除1例无功能胰腺内分泌肿瘤患者外,所有神经内分泌肿瘤患者的嗜铬粒蛋白A均升高(均值为每1单位401±409)。BPH患者与神经内分泌肿瘤患者(p<0.01)、前列腺癌患者与神经内分泌肿瘤患者(p<0.01)以及BPH患者与前列腺癌患者(p<0.05)之间的血浆嗜铬粒蛋白A水平存在显著差异。33例前列腺癌患者中有5例嗜铬粒蛋白A升高,其中只有1例前列腺特异性抗原升高。

结论

嗜铬粒蛋白A是神经内分泌肿瘤,尤其是无功能肿瘤的优秀标志物,对于检测前列腺特异性抗原未升高患者的前列腺癌,测定嗜铬粒蛋白A也很有用。

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2
Metastatic prostate cancer with normal level of serum prostate-specific antigen.
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