生长激素受体在脑肿瘤中的表达。

Q4 Medicine
Tetsuhiko Sakoguchi, Seiji Hama, Atsushi Tominaga, Yasuyuki Kinoshita, Kazuhiko Sugiyama, Kazunori Arita, Kaoru Kurisu
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引用次数: 0

摘要

生长激素(GH)对儿童和成人的生活质量至关重要,但它也被认为能促进各种肿瘤的生长。然而,生长激素在大脑中的作用,特别是在脑肿瘤中的作用,尚未确定。为了从受体表达的角度阐明这些问题,我们利用免疫组织化学方法检测了GH受体(GHR)在脑肿瘤中的表达,并分析了GHR表达与临床特征的关系。从脑肿瘤患者(106例垂体腺瘤、12例颅咽管瘤、13例生殖细胞瘤、6例髓母细胞瘤和12例恶性胶质瘤)的手术标本中检测GHR的免疫组织化学表达。恶性肿瘤的GHR阳性率低于良性肿瘤(垂体腺瘤59%,颅咽管瘤73%,生殖细胞瘤23%,髓母细胞瘤和胶质瘤0%)。垂体腺瘤的GHR染色较正常垂体弱。在产生ghr的垂体腺瘤中,ghr阳性和阴性肿瘤的大小没有差异。然而,在不产生ghr的腺瘤中,ghr阳性的肿瘤明显较小。因此,免疫组织化学GHR表达可能至少在一定程度上对脑肿瘤的生长潜力有负面影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Growth hormone receptor expression in brain tumors.

Growth hormone (GH) is essential for quality of life in both children and adults, but it is also believed to enhance the growth of various neoplasms. However, the role of GH in the brain, particularly in brain tumors, has yet to be established. To clarify these problems from the perspective of receptor expression, we examined GH receptor (GHR) expression in brain tumors using immunohistochemistry and the correlation between GHR expression and clinical features. Surgical specimens obtained from patients with brain tumors (106 pituitary adenomas, 12 craniopharyngiomas, 13 germ cell tumors, 6 medulloblastomas, and 12 malignant gliomas) were examined immunohistochemically for GHR expression. The GHR positive rate was lower in malignant tumors than in benign tumors (59% in pituitary adenomas, 73% in craniopharyngiomas, 23% in germ cell tumors, and 0% in medulloblastomas and gliomas). GHR staining in pituitary adenomas was weaker than that in normal pituitary gland. Among the GH-producing pituitary adenomas, there was no difference in size between GHR-positive and -negative tumors. However, among the non-GH-producing adenomas, GHR-positive tumors were significantly smaller. Thus, immunohistochemical GHR expression may have, at least in part, a negative impact on tumor growth potential in brain tumors.

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来源期刊
Hiroshima journal of medical sciences
Hiroshima journal of medical sciences Medicine-Medicine (all)
CiteScore
0.30
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