Karjalainen J M, Kellokoski J K, Mannermaa A J, Kujala H E, Moisio K I, Mitchell P J, Eskelinen M J, Alhava E M, Kosma V M
Department of Surgery, University of Kuopio and Kuopio University Hospital, Finland.
Br J Cancer. 2000 Jun;82(12):2015-21. doi: 10.1054/bjoc.2000.1145.
The loss of transcription factor AP-2alpha expression has been shown to associate with tumourigenicity of melanoma cell lines and poor prognosis in primary cutaneous melanoma. Altogether these findings suggest that the gene encoding AP-2alpha (TFAP2A) acts as a tumour suppressor in melanoma. To learn more of AP-2alpha's down-regulation mechanisms, we compared the immunohistochemical AP-2alpha protein expression patterns with the corresponding mRNA expression detected by in situ hybridization in 52 primary melanomas. Of the 25 samples with AP-2alpha protein negative areas, 16 (64%) expressed mRNA throughout the consecutive section. Nine specimens (36%) contained equally mRNA- and protein-negative areas, suggesting that the loss of AP-2alpha protein associated with lack of the mRNA transcript. The highly AP-2alpha protein-positive tumours (n = 27) were concordantly mRNA positive in 25 (92.6%) cases. Thirteen primary tumours were further analysed using microsatellite markers D6S470 and D6S263 for loss of heterozygosity (LOH) of a locus harbouring TFAP2A. LOHs or chromosome 6 monosomy were found in four out of five (80%) informative AP-2alpha mRNA- and protein-negative tumour areas, but also within five out of 13 (38%) informative AP-2alpha mRNA-positive tumour areas. This chromosome region is thus suggestive of harbouring a putative tumour suppressor gene of cutaneous melanoma, but this referring specifically to TFAP2A could not be completely verified in this analysis. We conclude that a failure in post-transcriptional processing of AP-2alpha is a possible inactivation mechanism of AP-2alpha in cutaneous melanoma.
转录因子AP - 2α表达缺失已被证明与黑色素瘤细胞系的致瘤性及原发性皮肤黑色素瘤的不良预后相关。这些发现共同表明,编码AP - 2α的基因(TFAP2A)在黑色素瘤中起肿瘤抑制作用。为了进一步了解AP - 2α的下调机制,我们在52例原发性黑色素瘤中,将免疫组化检测的AP - 2α蛋白表达模式与原位杂交检测的相应mRNA表达进行了比较。在25个存在AP - 2α蛋白阴性区域的样本中,16个(64%)在连续切片中均表达mRNA。9个样本(36%)同时存在mRNA和蛋白阴性区域,这表明AP - 2α蛋白缺失与mRNA转录本缺失相关。AP - 2α蛋白高度阳性的肿瘤(n = 27)中,25个(92.6%)病例的mRNA同样呈阳性。使用微卫星标记D6S470和D6S263对13例原发性肿瘤进行进一步分析,以检测含有TFAP2A的位点的杂合性缺失(LOH)。在5个提供信息的AP - 2α mRNA和蛋白阴性肿瘤区域中,有4个(80%)发现了LOH或6号染色体单体,但在13个提供信息的AP - 2α mRNA阳性肿瘤区域中也有5个(38%)发现了LOH。因此,该染色体区域提示可能存在皮肤黑色素瘤的一个假定肿瘤抑制基因,但在本分析中无法完全证实该基因具体就是TFAP2A。我们得出结论,AP - 2α转录后加工失败是皮肤黑色素瘤中AP - 2α失活的一种可能机制。