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一种在恶性潜能较低的黑色素瘤细胞中表达的肿瘤相关抗原。

A tumor-associated antigen expressed in melanoma cells with lower malignant potential.

作者信息

Suter L, Brüggen J, Bröcker E B, Sorg C

出版信息

Int J Cancer. 1985 Jun 15;35(6):787-91. doi: 10.1002/ijc.2910350615.

DOI:10.1002/ijc.2910350615
PMID:3891640
Abstract

The antigen K-1-2, detectable by a MAb is found in nevi and melanomas. It is associated with melanoma cells of low invasive and metastatic potential as shown by immunoperoxidase studies with cell lines, biopsies and autopsies: K-1-2 occurs in melanoma cell line SK-Mel 25, but not in cell line A-375. A-375 has a higher malignant potential than SK-Mel 25 because, in contrast to SK-Mel 25, it produces plasminogen activator and grows in nude mice. K-1-2 was frequently strongly expressed (greater than or equal to 50% cells positive) in flat (less than 1.5 mm) and less frequently in medium and thick primary tumors. In thick primary melanomas K-1-2 positive cells were confined to the junctional zone or to marginal, flat areas of the tumor. Only rarely does K-1-2 occur in metastases. Strong expression of the K-1-2 antigen was found less often in primary melanomas, which develop early metastases, than in tumors that had not metastasized during an observation period of 18 months. In 5 patients with disseminated metastatic disease, metastases strongly expressing K-1-2 and those negative for this marker or containing only a minor percentage of K-1-2 positive cells were observed simultaneously or at different times. These findings suggest that a change from high malignancy to low malignancy--as observed in animal systems--may also occur in human melanoma.

摘要

一种单克隆抗体可检测到的抗原K-1-2存在于痣和黑色素瘤中。免疫过氧化物酶研究(针对细胞系、活检组织和尸检)表明,它与低侵袭性和转移潜能的黑色素瘤细胞相关:K-1-2存在于黑色素瘤细胞系SK-Mel 25中,但不存在于细胞系A-375中。A-375的恶性潜能高于SK-Mel 25,因为与SK-Mel 25不同,它能产生纤溶酶原激活物并能在裸鼠体内生长。K-1-2在扁平的(小于1.5毫米)原发性肿瘤中经常强表达(≥50%细胞呈阳性),而在中等厚度和厚的原发性肿瘤中表达频率较低。在厚的原发性黑色素瘤中,K-1-2阳性细胞局限于交界区或肿瘤的边缘扁平区域。K-1-2很少出现在转移灶中。与在18个月观察期内未发生转移的肿瘤相比,在早期发生转移的原发性黑色素瘤中,K-1-2抗原的强表达较少见。在5例播散性转移性疾病患者中,同时或在不同时间观察到了强表达K-1-2的转移灶以及该标志物阴性或仅含少量K-1-2阳性细胞的转移灶。这些发现表明,正如在动物系统中观察到的那样,人类黑色素瘤中也可能发生从高恶性到低恶性的转变。

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Tumour necrosis factors and several interleukins inhibit the growth and modulate the antigen expression of normal human melanocytes in vitro.肿瘤坏死因子和几种白细胞介素在体外可抑制正常人黑素细胞的生长并调节其抗原表达。
Arch Dermatol Res. 1995;287(3-4):259-65. doi: 10.1007/BF01105076.
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Modulation of melanoma-associated antigens by monoclonal antibodies as visualized by radioimmunoelectron microscopy and radioantibody binding assay.
通过放射免疫电子显微镜和放射抗体结合试验观察单克隆抗体对黑色素瘤相关抗原的调节作用。
Arch Dermatol Res. 1987;279 Suppl:S116-26. doi: 10.1007/BF00585934.
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Radioimmunotherapy of malignancy using antibody targeted radionuclides.使用抗体靶向放射性核素进行恶性肿瘤的放射免疫治疗。
Br J Cancer. 1986 Dec;54(6):863-70. doi: 10.1038/bjc.1986.254.
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