Jr. Turner et al., Preoperative chemoradiotherapy alters the expression and prognostic significance of adhesion molecules in Barrett's-associated adenocarcinoma, HUMAN PATH, 31(3), 2000, pp. 347-353
Citations number
31
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
A variety of prognostic markers have been related to decreased patient surv
ival in patients: with epithelial malignancies. These include expression of
the homotypic adhesion molecule E-cadherin (ECAD) and the hyaluronic acid
receptor CD44. Expression of ECAD and CD44 was evaluated in Barrett's-assoc
iated adenocarcinoma (BAd) from 67 patients. Expression was determined by i
mmunoperoxidase staining and graded semiquantitatively based on the proport
ion of positively stained cells. These data were then correlated with clini
cal and pathological parameters, including the presence or absence of chemo
radiotherapy (chemrad) and patient survival. There were 56 men and 11 women
(mean age, 62 years). Thirty-nine (58%) patients received preoperative che
mrad. ECAD expression was detected in all (100%) tumors. The ECAD staining
grade did not correlate with other pathological features of the tumors. How
ever, ECAD staining was significantly increased in BAd of patients who rece
ived chemrad (P = .003), in comparison with those who did not, and in indiv
idual patients when prechemrad biopsies and postchemrad resection specimens
were compared (P = .04). In terms of prognosis, increased ECAD expression
was associated with shortened patient survival only in BAd patients who had
received chemrad (univariate analysis of chemrad patients with stage I and
II BAd, P = .02). ECAD expression was not significantly associated with su
rvival in BAd patients who did not receive chemrad. CD44 expression was det
ected in 88% of cases, CD44 expression did not correlate with any of the pa
thological features of the tumors or with chemrad status. Increased express
ion of CD44 was significantly associated with shortened patient survival in
chemrad patients only (univariate analysis P = .03, multivariate analysis
P = .04), although a strong trend was observed when all patients were analy
zed regardless of chemrad status (P = .07). The results of this study indic
ate that chemrad alters the expression of ECAD in BAd. Thus, the prognostic
utility of ECAD expression must be evaluated in the context of chemrad sta
tus. CD44 also may be a valuable prognostic marker in BAd. Copyright (C) 20
00 by W.B. Saunders Company.