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人黑色素瘤蛋白聚糖:在由内在和外在信号控制的杂交体中的表达。

Human melanoma proteoglycan: expression in hybrids controlled by intrinsic and extrinsic signals.

作者信息

Rettig W J, Real F X, Spengler B A, Biedler J L, Old L J

出版信息

Science. 1986 Mar 14;231(4743):1281-4. doi: 10.1126/science.3633135.

DOI:10.1126/science.3633135
PMID:3633135
Abstract

Human malignant melanoma cells express specific chondroitin sulfate proteoglycans (mel-CSPG) on the surface, both in vivo and in vitro. Melanocytes in normal skin show no detectable mel-CSPG but can be induced to express the antigen when cultured in the presence of cholera toxin and the tumor promoter 12-O-tetradecanoylphorbol-13-acetate. Most other cell types do not express mel-CSPG either in vivo or in vitro. A study was designed to examine regulatory signals controlling mel-CSPG expression. The gene encoding mel-CSPG was mapped to human chromosome 15, and this chromosome was introduced into rodent cells derived from distinct differentiation lineages. Three types of mel-CSPG--expressing hybrids were found: (i) hybrids derived from human melanomas; (ii) hybrids derived from human cells that do not express mel-CSPG; and (iii) hybrids derived from human cells expressing mel-CSPG that are antigen-negative but that are induced to express mel-CSPG when cultured on extracellular matrix instead of plastic surfaces. Thus, mel-CSPG expression can be controlled both through intrinsic signals, provided by the differentiation program of the rodent fusion partner, and through extrinsic signals, provided by specific cell-matrix interactions.

摘要

人类恶性黑色素瘤细胞在体内和体外均在表面表达特定的硫酸软骨素蛋白聚糖(mel-CSPG)。正常皮肤中的黑素细胞未检测到mel-CSPG,但在霍乱毒素和肿瘤启动子十四烷酰佛波醇乙酯存在的情况下培养时可被诱导表达该抗原。大多数其他细胞类型在体内或体外均不表达mel-CSPG。设计了一项研究来检查控制mel-CSPG表达的调节信号。编码mel-CSPG的基因被定位到人类15号染色体上,并将该染色体导入源自不同分化谱系的啮齿动物细胞中。发现了三种表达mel-CSPG的杂种细胞:(i)源自人类黑色素瘤的杂种细胞;(ii)源自不表达mel-CSPG的人类细胞的杂种细胞;(iii)源自表达mel-CSPG但抗原阴性的人类细胞的杂种细胞,这些细胞在细胞外基质而非塑料表面上培养时被诱导表达mel-CSPG。因此,mel-CSPG的表达既可以通过啮齿动物融合伙伴的分化程序提供的内在信号来控制,也可以通过特定细胞-基质相互作用提供的外在信号来控制。

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引用本文的文献

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Theranostic impact of NG2/CSPG4 proteoglycan in cancer.NG2/CSPG4蛋白聚糖在癌症中的诊疗意义
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2
CSPG4 protein as a new target for the antibody-based immunotherapy of triple-negative breast cancer.CSPG4 蛋白作为三阴性乳腺癌抗体免疫治疗的新靶点。
J Natl Cancer Inst. 2010 Oct 6;102(19):1496-512. doi: 10.1093/jnci/djq343. Epub 2010 Sep 17.
3
Recent advances in the treatment of malignant melanoma with gene therapy.基因治疗在恶性黑色素瘤治疗中的最新进展。
Mol Med. 1997 Oct;3(10):636-51.
4
Molecular cloning of a human melanoma-associated chondroitin sulfate proteoglycan.一种人类黑色素瘤相关硫酸软骨素蛋白聚糖的分子克隆
Proc Natl Acad Sci U S A. 1996 Sep 3;93(18):9710-5. doi: 10.1073/pnas.93.18.9710.
5
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Hum Genet. 1993 Nov;92(5):516-8. doi: 10.1007/BF00216462.
6
Extracellular matrix-modulated expression of human cell surface glycoproteins A42 and J143. Intrinsic and extrinsic signals determine antigenic phenotype.细胞外基质调节人细胞表面糖蛋白A42和J143的表达。内在和外在信号决定抗原表型。
J Exp Med. 1986 Nov 1;164(5):1581-99. doi: 10.1084/jem.164.5.1581.
7
Effects of extracellular matrix on the malignant phenotype.细胞外基质对恶性表型的影响。
Yale J Biol Med. 1988 Jan-Feb;61(1):35-8.
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Cell surface molecules of human melanoma. Immunohistochemical analysis of the gp57, GD3, and mel-CSPG antigenic systems.人类黑色素瘤的细胞表面分子。gp57、GD3和黑色素瘤硫酸软骨素蛋白聚糖抗原系统的免疫组织化学分析。
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Two human melanoma xenografts with different metastatic capacity and glycosaminoglycan pattern.两种具有不同转移能力和糖胺聚糖模式的人黑色素瘤异种移植瘤。
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