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表皮生长因子受体在人移行细胞癌中的表达的临床意义

Clinical implications of the expression of epidermal growth factor receptors in human transitional cell carcinoma.

作者信息

Messing E M

机构信息

Department of Surgery and Human Oncology, University of Wisconsin School of Medicine, Madison 53792.

出版信息

Cancer Res. 1990 Apr 15;50(8):2530-7.

PMID:1690599
Abstract

To evaluate the distribution and density of epidermal growth factor (EGF) receptors (EGF-Rs) on urothelium, immunohistological studies using a monoclonal antibody to the binding portion of the human EGF-R were performed on frozen specimens of normal urothelium (N = 20), urothelium from patients with nonurothelial urological malignancies (N = 15) and inflammatory diseases (N = 8), low grade superficial transitional cell carcinomas (TCC) (N = 13), high grade superficial or invasive TCC (N = 28), and endoscopically normal appearing urothelium from patients with low grade superficial (N = 5) or high grade (N = 21) TCC elsewhere in the bladder (or ipsilateral renal pelvis/ureter). EGF-Rs are found only on the basal layer of epithelial cells (with scattered representation on intermediate cells) in 95% of normal urothelial specimens and 100% of pathological specimens without urothelial malignancy. Alternatively, 92.3% of specimens of low grade superficial TCC and 100% of high grade TCCs had EGF-Rs richly expressed on the superficial as well as the deeper layers of urothelium. This "malignant" distribution of EGF-Rs was also found on all specimens of endoscopically normal appearing urothelium in patients with TCC elsewhere. The density of EGF-Rs correlated closely with tumor grade on both "premalignant" and frankly neoplastic urothelium. We conclude that the expression of EGF-Rs on urothelium favors the interaction of premalignant and malignant tissue with urinary EGF. To determine if altering the physiochemical environment of urine could interfere with this interaction, the effects of pH on the binding of and growth responses to EGF were assessed on four human TCC cell lines. Scatchard plots demonstrated that varying pH from 5.0 to 7.5 did not significantly change the total number of receptors, but EGF-R affinity was reduced approximately 20-fold as pH decreased from 7.5 to 5 in each TCC target. Similarly, significant growth stimulation by EGF at pH 7.5 was abrogated at pH less than or equal to 7.0 while growth rates in the absence of EGF remained unchanged at lower pHs. It thus appears that urinary acidification may hold promise in the management and prevention of recurrent bladder cancer.

摘要

为评估表皮生长因子(EGF)受体(EGF-Rs)在尿路上皮的分布及密度,我们使用针对人EGF-R结合部分的单克隆抗体,对正常尿路上皮的冰冻标本(N = 20)、非尿路上皮性泌尿系统恶性肿瘤患者的尿路上皮(N = 15)、炎症性疾病患者的尿路上皮(N = 8)、低级别浅表性移行细胞癌(TCC)(N = 13)、高级别浅表性或浸润性TCC(N = 28)以及膀胱其他部位(或同侧肾盂/输尿管)患有低级别浅表性(N = 5)或高级别(N = 21)TCC患者的内镜下外观正常的尿路上皮进行了免疫组织学研究。在95%的正常尿路上皮标本和100%无尿路上皮恶性肿瘤的病理标本中,EGF-Rs仅在上皮细胞的基底层发现(中间细胞有散在分布)。相反,92.3%的低级别浅表性TCC标本和100%的高级别TCC标本在尿路上皮的表层及深层均有丰富的EGF-Rs表达。在其他部位患有TCC患者的所有内镜下外观正常的尿路上皮标本中也发现了这种EGF-Rs的“恶性”分布。在“癌前”和明显肿瘤性尿路上皮中,EGF-Rs的密度与肿瘤分级密切相关。我们得出结论,尿路上皮中EGF-Rs的表达有利于癌前和恶性组织与尿中EGF的相互作用。为确定改变尿液的理化环境是否会干扰这种相互作用,我们评估了pH值对四种人TCC细胞系中EGF结合及生长反应的影响。Scatchard图显示,将pH值从5.0改变至7.5并未显著改变受体总数,但在每个TCC靶细胞中,随着pH值从7.5降至5,EGF-R亲和力降低了约20倍。同样,在pH值为7.5时EGF显著的生长刺激作用在pH值小于或等于7.0时消失,而在较低pH值下无EGF时的生长速率保持不变。因此,尿液酸化在复发性膀胱癌的管理和预防中可能具有前景。

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