Molecular analyses of sentinel lymph nodes: an open question

被引:9
作者
Bonin, S [1 ]
Niccolini, B
Calacione, R
Gambardella, B
Geatti, O
Stanta, G
Trevisan, G
机构
[1] Univ Trieste, Osped Cattinara, Dept Clin Morphol & Technol Sci, Unit Dermatol, I-34127 Trieste, Italy
[2] Univ Trieste, Osped Cattinara, Dept Clin Morphol & Technol Sci, Unit Surg Pathol, I-34127 Trieste, Italy
[3] Int Ctr Genet Engn & Biotechnol, I-34012 Trieste, Italy
[4] Maggiore Hosp, Surg Unit, Trieste, Italy
[5] Maggiore Hosp, Nucl Med Unit, Trieste, Italy
关键词
multiple markers; paraffin-embedded tissues; reverse transcriptase-polymerase chain reaction;
D O I
10.1046/j.1468-3083.2002.00360.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Aims To detect micrometastases in the sentinel lymph nodes (SLN) of melanoma patients the authors analysed 52 lymph nodes (47 SLNs and five non-sentinel) and 17 corresponding primary skin melanomas using reverse transcriptase-polymerase chain reaction assays in paraffin-embedded tissues to detect the mRNAs of tyrosinase, MAGE1, MAGE3, MIA, MART-1 and mRNA coding for telomerase catalytic component. Results Our data show that the use of molecular markers for melanoma micrometastases detection in SLN is still in a very preliminary stage. In comparing the molecular analysis results with the pathological staging we did not find any evident correlation with the expression of the analysed genes in SLN. There are no data for judging the prognostic significance of the detection of circulating tumour cells in patients without clinically recognizable metastases. Despite progress in the field with simultaneous detection of several markers it was assumed that tyrosinase mRNA remains the best target for the detection of metastatic melanoma cells.
引用
收藏
页码:34 / 39
页数:6
相关论文
共 21 条
[1]  
BERGMANN U, 1995, CANCER RES, V55, P2007
[2]  
BLATHEA HJ, 1998, INT J CANC PRED ONCO, V79, P318
[3]   Prognostic significance of occult metastases detected by sentinel lymphadenectomy and reverse transcriptase-polymerase chain reaction in early-stage melanoma patients [J].
Bostick, PJ ;
Morton, DL ;
Turner, RR ;
Huynh, KT ;
Wang, HJ ;
Elashoff, R ;
Essner, R ;
Hoon, DSB .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (10) :3238-3244
[4]   EXPRESSION OF MAGE GENES IN PRIMARY AND METASTATIC CUTANEOUS MELANOMA [J].
BRASSEUR, F ;
RIMOLDI, D ;
LIENARD, D ;
LETHE, B ;
CARREL, S ;
ARIENTI, F ;
SUTER, L ;
VANWIJCK, R ;
BOURLOND, A ;
HUMBLET, Y ;
VACCA, A ;
CONESE, M ;
LAHAYE, T ;
DEGIOVANNI, G ;
DERAEMAECKER, R ;
BEAUDUIN, M ;
SASTRE, X ;
SALAMON, E ;
DRENO, B ;
JAGER, E ;
KNUTH, A ;
CHEVREAU, C ;
SUCIU, S ;
LACHAPELLE, JM ;
POUILLART, P ;
PARMIANI, G ;
LEJEUNE, F ;
CEROTTINI, JC ;
BOON, T ;
MARCHAND, M .
INTERNATIONAL JOURNAL OF CANCER, 1995, 63 (03) :375-380
[5]  
Dalerba P, 1998, INT J CANCER, V77, P200, DOI 10.1002/(SICI)1097-0215(19980717)77:2<200::AID-IJC5>3.0.CO
[6]  
2-U
[7]   Melanoma-inhibiting activity (MIA) mRNA is not exclusively transcribed in melanoma cells: low levels of MIA mRNA are present in various cell types and in peripheral blood [J].
de Vries, TJ ;
Fourkour, A ;
Punt, CJA ;
Diepstra, H ;
Ruiter, DJ ;
van Muijen, GNP .
BRITISH JOURNAL OF CANCER, 1999, 81 (06) :1066-1070
[8]   Review: Polymerase chain reaction detection of micrometastases and circulating tumor cells: Application to melanoma, prostate, and thyroid carcinomas [J].
Ghossein, RA ;
Carusone, L ;
Bhattacharya, S .
DIAGNOSTIC MOLECULAR PATHOLOGY, 1999, 8 (04) :165-175
[9]   Telomerase activity in pancreatic endocrine tumours: a potential marker for malignancy [J].
Lam, KY ;
Lo, CY ;
Fan, ST ;
Luk, JM .
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 2000, 53 (03) :133-136
[10]   Sentinel lymph node biopsy in patients with primary cutaneous melanoma: study of 455 cases [J].
Landi, G ;
Polverelli, M ;
Moscatelli, G ;
Morelli, R ;
Landi, C ;
Fiscelli, O ;
Erbazzi, A .
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2000, 14 (01) :35-45