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用重组刺猬蛋白相互作用蛋白对基底细胞癌进行免疫预防。

Immunoprevention of basal cell carcinomas with recombinant hedgehog-interacting protein.

作者信息

Vogt Annika, Chuang Pao-Tien, Hebert Jennifer, Hwang Jimmy, Lu Ying, Kopelovich Levy, Athar Mohammad, Bickers David R, Epstein Ervin H

机构信息

Department of Dermatology, University of California San Francisco, 94143, USA.

出版信息

J Exp Med. 2004 Mar 15;199(6):753-61. doi: 10.1084/jem.20031190.

Abstract

Basal cell carcinomas (BCCs) are driven by abnormal hedgehog signaling and highly overexpress several hedgehog target genes. We report here our use of one of these target genes, hedgehog-interacting protein (Hip1), as a tumor-associated antigen for immunoprevention of BCCs in Ptch1+/- mice treated with ionizing radiation. Hip1 mRNA is expressed in adult mouse tissues at levels considerably lower than those in BCCs. Immunization with either of two large recombinant Hip1 polypeptides was well tolerated in Ptch1+/- mice, induced B and T cell responses detectable by enzyme-linked immunosorbent assay, Western blot, delayed type hypersensitivity, and enzyme-linked immunospot assay, and reduced the number of BCCs by 42% (P < 0.001) and 32% (P < 0.01), respectively. We conclude that immunization with proteins specifically up-regulated by hedgehog signaling may hold promise as a preventive option for patients such as those with the basal cell nevus syndrome who are destined to develop large numbers of BCCs.

摘要

基底细胞癌(BCCs)由异常的刺猬信号通路驱动,并高度过表达多个刺猬信号靶基因。我们在此报告,我们使用这些靶基因之一的刺猬相互作用蛋白(Hip1),作为肿瘤相关抗原,用于对接受电离辐射的Ptch1+/-小鼠进行BCCs的免疫预防。Hip1 mRNA在成年小鼠组织中的表达水平明显低于BCCs中的表达水平。用两种大型重组Hip1多肽中的任何一种进行免疫,在Ptch1+/-小鼠中耐受性良好,通过酶联免疫吸附测定、蛋白质印迹、迟发型超敏反应和酶联免疫斑点测定可检测到诱导的B细胞和T细胞反应,并且BCCs的数量分别减少了42%(P < 0.001)和32%(P < 0.01)。我们得出结论,用由刺猬信号通路特异性上调的蛋白质进行免疫,对于像基底细胞痣综合征患者这类注定会发生大量BCCs的患者,可能有望成为一种预防选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7637/2212732/d7453c4962f4/20031190f1.jpg

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