Detection of telomerase activity and correlation with mitotic and apoptotic indices, Ki-67 and expression of cyclins D1 and A in cutaneous melanoma

Citation
C. Miracco et al., Detection of telomerase activity and correlation with mitotic and apoptotic indices, Ki-67 and expression of cyclins D1 and A in cutaneous melanoma, INT J CANC, 88(3), 2000, pp. 411-416
Citations number
52
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF CANCER
ISSN journal
00207136 → ACNP
Volume
88
Issue
3
Year of publication
2000
Pages
411 - 416
Database
ISI
SICI code
0020-7136(20001101)88:3<411:DOTAAC>2.0.ZU;2-6
Abstract
Telomerase plays a key role in carcinogenesis. It is activated in most immo rtal cell lines and human cancers, including cutaneous melanoma (CM). Incre ased cell proliferation and deregulation of the cell cycle occur in human c ancers. Links between telomerase activity (TA), cell proliferation, cell de ath and expression of cell-cycle regulators have not been extensively eluci dated in CM. In this study, we investigated TA, mitotic index (MI), apoptot ic index (AI), Ki-67 and nuclear positivity of cyclins D1 and A (Ki-67+N/1, 000, cyclin D1+N/1,000, cyclin A+N/1,000) in 42 primary cutaneous melanomas (PCMs). TA was detected in all cases and directly correlated with MI, Ki-6 7+N/1,000, cyclin D1+N/1,000 and cyclin A+N/1,000 (p < 0.001); it was not c orrelated with AI. When subdividing PCMs into radial and vertical growth ph ase melanomas (RGPMs, VGPMs), a correlation was maintained only with MI (p < 0.005) and cyclin D1+N/1,000 (p < 0.005). Although MI and Ki-67+N/1,000 w ere highly correlated with cyclin D1+N1/,000 and cyclin A+N/1,000 (p < 0.00 1) when considering all cases together, a high correlation was found in the RGPM and VGPM groups between cyclin A+N/1,000 and Ki-67+N/1,000 only (p < 0.001), thus suggesting that cyclin A is more closely correlated with cell proliferation than cyclin D1. Our results further support the association b etween TA, tumor cell proliferation and cyclin D1 and A expression in PCM, though it is possible that links between TA and proliferation, on the one h and, and TA and cyclin D1 expression, on the other, might occur following v arious pathways. Int. J. Cancer 88:411-416, 2000. (C) 2000 Wiley-Liss, Inc.