Growth hormone and gastrointestinal malignancy: An intriguing link
Rajan Palui1, Kalyani Sridharan2, Sadishkumar Kamalanathan3
1Department of Endocrinology, The Mission Hospital, Durgapur 713212, West Bengal, India.
World Journal of Gastrointestinal Pathophysiology
|February 6, 2023
Summary
Growth hormone (GH) excess increases gastrointestinal (GI) neoplasm risk, particularly colorectal. While GH and IGF-1 signaling promote cell growth, mortality rates may not differ from controls, warranting screening for acromegaly patients.
Area of Science:
- Endocrinology
- Gastroenterology
- Oncology
Background:
- Growth hormone (GH) excess, as seen in acromegaly, is linked to systemic complications, including a higher risk of gastrointestinal (GI) neoplasms.
- Colorectal adenomas and carcinomas are the most frequently reported GI neoplasms associated with GH excess.
Purpose of the Study:
- To review the association between GH excess and GI neoplasms.
- To explore pathogenic mechanisms and clinical management guidelines for colorectal neoplasms in patients with GH excess.
Main Methods:
- Literature review of studies investigating GH excess and GI neoplasms.
- Analysis of pathogenic mechanisms including GH-IGF-1 signaling, and other contributing factors.
- Examination of current screening and follow-up colonoscopy guidelines for acromegaly patients.
Main Results:
- GH excess is associated with an increased incidence of GI neoplasms, particularly colorectal adenomas and carcinomas.
- Pathogenic mechanisms involve GH-Insulin-like Growth Factor 1 (IGF-1) signaling, promoting proliferation and inhibiting apoptosis.
- Conflicting data exists on colon cancer-specific mortality, with some recent studies showing no difference compared to controls.
Conclusions:
- Acromegaly patients with GH excess have an increased risk of GI neoplasms, necessitating initial screening colonoscopies.
- Follow-up colonoscopy recommendations vary based on initial findings and GH excess remission status.
- Current evidence does not indicate an increased risk of colorectal cancer in patients receiving recombinant GH therapy.
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