Carvalho Lucia, Lipay Monica, Belfort Francisco, Santos Ivan, Andrade Joyce, Haddad Alessandra, Brunstein Flavia, Ferreira Lydia
Surgery Department, Plastic Surgery Division, UNIFESP, Federal University of São Paulo, São Paulo, SP, Brazil.
J Plast Reconstr Aesthet Surg. 2006;59(9):961-8. doi: 10.1016/j.bjps.2006.01.022. Epub 2006 Apr 3.
Telomerase activity (TA) is believed to play a role in the regulation of senescence and to limit the number of cell divisions. The deregulation of telomerase appears to contribute to oncogenesis and the formation of immortal cell lines. As a result, it is believed that it could be used as a prognostic marker in melanoma.
TA was assayed by the polymerase chain reaction PCR-ELISA-based telomeric repeat amplification protocol (TRAP assay). One hundred and eight samples were distributed in four histological groups: 30 samples from primary cutaneous melanomas, 24 from peritumoural skin sites, 28 from benign melanocytic lesions, and 26 from normal skin sites as a control.
TA was different among the four tested groups (Kruskall-Wallis test p<0.001), and increasing values of TA were observed progressing from normal skin to benign and then to malignant lesions. Among melanoma samples, there was a significant association between TA and ulceration (p=0.025), TA and vascular invasion (p=0.018) and TA and mitotic rate (p=0.029) (Mann-Whitney test). A linear regression analysis showed significant associations between the increase of TA with Breslow thickness (p=0.004) and the presence of satellites (p=0.002).
We observed that TA had increased from control skin to peritumoural skin, and then to benign melanocytic lesions and finally to melanoma, suggesting tumour progression. TA showed higher values in the presence of some important histopathologic parameters related to poor prognosis in cutaneous melanoma such as ulceration, vascular invasion, satellites, high rates of mitosis, and in thicker tumours.
端粒酶活性(TA)被认为在衰老调节中起作用,并限制细胞分裂次数。端粒酶失调似乎有助于肿瘤发生和永生细胞系的形成。因此,人们认为它可作为黑色素瘤的预后标志物。
采用基于聚合酶链反应PCR-ELISA的端粒重复序列扩增法(TRAP法)检测TA。108个样本分为四个组织学组:30个原发性皮肤黑色素瘤样本、24个肿瘤周围皮肤样本、28个良性黑素细胞病变样本和26个正常皮肤样本作为对照。
四组检测结果中TA不同(Kruskal-Wallis检验p<0.001),从正常皮肤到良性病变再到恶性病变,TA值逐渐升高。在黑色素瘤样本中,TA与溃疡(p=0.025)、TA与血管侵犯(p=0.018)以及TA与有丝分裂率(p=0.029)之间存在显著关联(Mann-Whitney检验)。线性回归分析显示TA升高与Breslow厚度(p=0.004)和卫星灶存在(p=0.002)之间存在显著关联。
我们观察到TA从对照皮肤到肿瘤周围皮肤,再到良性黑素细胞病变,最后到黑色素瘤逐渐升高,提示肿瘤进展。在存在一些与皮肤黑色素瘤预后不良相关的重要组织病理学参数时,如溃疡、血管侵犯、卫星灶、高有丝分裂率以及较厚肿瘤中,TA显示出较高值。