Article
Rectal epithelial apoptosis in familial adenomatous polyposis
patients treated with sulindac
J J Kellerd, G J A Offerhausc, M Polakd, S N Goodmanb, M L Zahurakb, L M Hylinda, S R Hamiltonc, F M Giardielloa
a Department of
Medicine, The Johns Hopkins University School of Medicine, Baltimore,
Maryland, USA, b Oncology Centre, The Johns Hopkins University
School of Medicine, Baltimore, Maryland, USA, c Department of Pathology, The
John Hopkins University School of Medicine, Baltimore, Maryland, USA, d Department of Pathology, Academic Medical
Centre, The Netherlands
Correspondence to: Dr F M Giardiello, The Johns Hopkins University, Room 431, 1830 East Monument Street, Baltimore, Maryland 21205, USA.
Accepted for publication 11 May 1999
BACKGROUND
Sulindac regresses
colorectal adenomas in patients with familial adenomatous polyposis
(FAP), although the mechanism of polyp regression is unclear.
AIMS
To determine whether
differences occur in alteration of rectal epithelial apoptotic index
and expression of apoptosis related proteins in FAP patients treated
with sulindac compared with placebo.
PATIENTS
Twenty one FAP patients;
12 had not undergone colectomy.
METHODS
Patients with FAP were
treated with sulindac 150 mg orally twice a day for three months (n=10)
or placebo (n=11). Colorectal polyp number was determined and biopsies
of the normal rectal mucosa were performed before and after three
months of treatment. Response to treatment and alteration of the
apoptotic ratio (index in base of crypt divided by index in surface
epithelium) were evaluated. Bcl-2, bax, p21/WAF-1, and p53 proteins
were assessed semiquantitatively by immunohistochemistry.
RESULTS
Significant decreases in
polyp number and in the apoptotic ratio were seen in patients treated
with sulindac compared with controls. The mean percentage change in
polyp number from baseline was
46% in the sulindac group and +13%
in the placebo group (p=0.005). Mean percentage change in the apoptotic
ratio was
8% and +25% in the sulindac and placebo treated
patients, respectively (p=0.004). No differences in expression or
compartmentalisation of apoptosis related proteins were noted between
treatment groups.
CONCLUSIONS
Sulindac regression of
colorectal adenomas is accompanied by alteration of the rectal
epithelial apoptotic ratio with relative increase in apoptosis in
surface cells compared with the deeper crypt. The utility of the
apoptotic ratio as an intermediate biomarker for colorectal
tumorigenesis deserves further study.
Keywords: apoptosis; familial adenomatous polyposis; sulindac; intermediate biomarker; tumorigenesis
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