Piérard G E, Piérard-Franchimont C
Department of Dermatopathology, CHU Sart Tilman, University of Liège, Belgium.
Eur J Cancer. 1997 Oct;33(11):1888-92. doi: 10.1016/s0959-8049(97)00231-1.
Tumour vascularity has been proposed as a prognostic indicator for a number of solid tumours. In these respects the situation is unclear for cutaneous malignant melanoma (MM). The small number of MM cases studied to date have indicated controversial preliminary conclusions. Hence, tumour thickness remains currently the most reliable prognostic factor for MM. This variable has been shown in previous work to be correlated with both the S-phase fraction and the growth fraction of the MM cells. We studied the relationship between vascularity and growth fraction of 100 thin (< 1 mm) cutaneous MM using immunohistochemistry (Ulex europaeus agglutinin-type 1 (UEA-1) and MIB-1 antibody (Ki-67)) and computerised image analysis. A stochastic relationship was found between intra- and peritumoral vascularity, and between Ki-67 and UEA-1 measures. Approximately 20-40% of PC-MM showing a high Ki-67-positive growth fraction (breakpoint: 30/0.4 mm2) were characterised by a prominent vascularity at the boundary of the neoplasm. In these cases, vessels often exhibited either heterogeneous lumen sizes or a uniform prominent dilated network. The present study shows that the angiogenic phenotype of MM occurs as a stochastic event during neoplastic progression. Its expression is not mandatory for reaching high values in MM growth fraction. It can be hypothesised that the absence of a link between proliferation and vascularity might account for the unusual outcome of some cutaneous MM, including the dormant growth-stunted type and the metastasising thin MM.
肿瘤血管生成已被提出作为多种实体瘤的预后指标。在这些方面,皮肤恶性黑色素瘤(MM)的情况尚不清楚。迄今为止,对少量MM病例的研究得出了有争议的初步结论。因此,肿瘤厚度目前仍是MM最可靠的预后因素。在先前的研究中已表明,这一变量与MM细胞的S期分数和生长分数均相关。我们使用免疫组织化学(荆豆凝集素1型(UEA-1)和MIB-1抗体(Ki-67))及计算机图像分析,研究了100例薄型(<1mm)皮肤MM的血管生成与生长分数之间的关系。在肿瘤内和肿瘤周围血管生成之间,以及Ki-67和UEA-1测量值之间发现了一种随机关系。约20-40% Ki-67阳性生长分数较高(断点:30/0.4 mm2)的PC-MM在肿瘤边界处具有显著的血管生成特征。在这些病例中,血管常表现为管腔大小不均或均匀显著扩张的网络。本研究表明,MM的血管生成表型在肿瘤进展过程中是一个随机事件。其表达并非MM生长分数达到高值所必需。可以推测,增殖与血管生成之间缺乏联系可能解释了一些皮肤MM的异常结局,包括休眠生长受阻型和转移性薄型MM。