A MOLECULAR EPIDEMIOLOGIC APPROACH TO THE STUDY OF EXPRESSION OF A METASTASIS MARKER IN PRIMARY MELANOMAS AND ITS CORRELATION WITH INDIVIDUAL PATIENTS RISK OF RECURRENCE OR METASTASIS
Jf. Dore et al., A MOLECULAR EPIDEMIOLOGIC APPROACH TO THE STUDY OF EXPRESSION OF A METASTASIS MARKER IN PRIMARY MELANOMAS AND ITS CORRELATION WITH INDIVIDUAL PATIENTS RISK OF RECURRENCE OR METASTASIS, Melanoma research, 7, 1997, pp. 121-125
Citations number
19
Categorie Soggetti
Medicine, Research & Experimental",Oncology,"Dermatology & Venereal Diseases
Tumour cells in malignant melanomas express molecules associated with
tumour progression; however, up until now, no marker has been able to
identify the tumour cells from which metastases are derived. It has re
cently been shown that in human melanoma cell lines, populations expre
ssing peanut agglutinin (PNA)-binding glycoproteins are able to genera
te metastases, and that such cells do exist in primary human melanomas
, their presence being associated with the degree of local invasion th
at governs the metastasis risk. To further investigate the correlation
between the expression of PNA-binding glycoconjugates by cells from p
rimary melanomas and the patient's individual risk of recurrence or me
tastasis, a molecular epidemiological approach employing histochemical
techniques within a case-control design was developed. The main objec
tive of this study is to determine whether an histochemical staining w
ith the lectin PNA of cells in the primary lesion is associated with a
n increased risk of local recurrence of metastasis, and with survival,
independently of Breslow's tumour thickness. The study comprises the
comparison of the PNA labelling index and of the type and intratumour
location of the staining as a function of clinical outcome in two matc
hed series of patients with known clinical outcome: patients who had d
ied at 5 years and patients alive at 5 years (to assess association wi
th survival), and patients who experienced a recurrence within the fir
st 5 years and patients alive without recurrence at 5 years (to assess
association with risk of recurrence). A matched case-control design w
as used with a variable number of controls matched to each case. Apart
from age (+/-5 years), sex and centre where diagnosis was made, match
ing was made on histogenetic type and primary tumour thickness (four c
ategories being considered: <0.75, 0.76-1.5, 1.513 and >3 mm).