Apoptosis is reduced in the colonic mucosa of patients with acromegaly
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Updated: Aug 14, 2026

Identification of Intracellular Signaling Events Induced in Viable Cells by Interaction with Neighboring Cells Undergoing Apoptotic Cell Death
Published on: December 27, 2016
Fausto Bogazzi1, Dania Russo, Maria Teresa Locci
1Department of Endocrinology and Metabolism, University of Pisa, Pisa, Italy. f.bogazzi@endoc.med.unipi.it
Background:
Patients with acromegaly have an increased risk of developing colonic tumours; reduced apoptosis is considered a leading mechanism in tumorigenesis. GH and IGF-1 decrease apoptosis in several cell lines including human colonic adenocarcinoma, but it is unknown whether epithelial cells of colonic mucosa of patients with acromegaly have reduced apoptosis.
Aim:
The aim of the study was to evaluate the degree of apoptosis in a cross-sectional study, in biopsy samples of colonic mucosa obtained from patients with acromegaly.
Patients And Methods:
Eleven patients with active, untreated acromegaly (AcroUntr), 16 patients with acromegaly in remission (AcroRem) and 23 controls were enrolled in the study. Samples of colonic mucosa were obtained during colonoscopy; apoptosis was evaluated by either DNA fragmentation or terminal deoxynucleotidyl transferase assay.
Results:
Apoptotic cells were 60.0 +/- 2.5% in samples of colonic mucosa of controls, 62.0 +/- 3.4% in those from patients with AcroRem (P = ns vs. controls), and 39.0 +/- 4.1% in those from patients with AcroUntr (P < 0.0001 vs. the other groups). Apoptosis was inversely related to serum IGF-I (r = 0.771, P < 0.001) or GH (r = 0.404, P = 0.05) levels and less to the estimated duration of disease (r = 0.384, P = 0.07). PPARgamma is considered to be a tumour suppressor gene the expression of which might be involved in colonic tumorigenesis. The expression of PPARgamma was lower in the colonic mucosa of patients with AcroUntr (2845 +/- 947 transcripts) than in that of controls (35 200 +/- 2450 transcripts) or AcroRem (29 547 +/- 3650 transcripts) (P < 0.005). The recovery of PPARgamma expression was associated with apoptosis in most cells. The lower degree of apoptosis in patients with AcroUntr was associated with a reduced expression of the antiapoptotic Bax protein.
Conclusion:
In conclusion, patients with AcroUntr have reduced apoptosis in colonic mucosa that is apparently reversed after acromegaly is cured. It is conceivable that reduced apoptosis may represent an early event in colonic tumorigenesis of patients with acromegaly.
Insights
Patients with active acromegaly show reduced apoptosis in colon cells, a condition reversed upon treatment. This suggests decreased apoptosis may be an early step in colon tumor development for acromegaly patients.
Area of Science:
- Endocrinology
- Gastroenterology
- Oncology
Background:
- Acromegaly increases colon tumor risk, with reduced apoptosis a suspected mechanism.
- While growth hormone (GH) and insulin-like growth factor-1 (IGF-1) reduce apoptosis in cell lines, its role in acromegaly patients' colonic mucosa was unclear.
Purpose of the Study:
- To evaluate apoptosis levels in colonic mucosa from acromegaly patients.
- To investigate the relationship between apoptosis, disease activity, and relevant molecular markers.
Main Methods:
- Cross-sectional study involving 11 untreated acromegaly patients, 16 in remission, and 23 controls.
- Colonic mucosa samples collected during colonoscopy.
- Apoptosis assessed via DNA fragmentation or terminal deoxynucleotidyl transferase assay; PPARgamma and Bax expression analyzed.
Main Results:
- Significantly reduced apoptosis (39.0%) in untreated acromegaly patients compared to controls (60.0%) and those in remission (62.0%).
- Apoptosis inversely correlated with serum IGF-1 and GH levels.
- Lower PPARgamma expression and reduced anti-apoptotic Bax protein observed in untreated patients.
Conclusions:
- Untreated acromegaly patients exhibit reduced colonic mucosal apoptosis, which normalizes after treatment.
- Decreased apoptosis may be an early event in colonic tumorigenesis associated with acromegaly.
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