Suter L, Brüggen J, Bröcker E B, Sorg C
Int J Cancer. 1985 Jun 15;35(6):787-91. doi: 10.1002/ijc.2910350615.
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.
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。