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MCM2 expression in serrated polyps demonstrates aberrant cellular proliferation
Danielle Fortuna1, Bruce Boman2, Raymond O'Neill1
1Department of Pathology, Thomas Jefferson University Hospital, PA 19107.
Human Pathology
|March 18, 2017
Summary
Serrated polyps, including hyperplastic polyps and sessile serrated adenomas, exhibit expanded proliferative compartments. Aberrant proliferation patterns in adjacent normal mucosa suggest a field effect, potentially promoting colorectal cancer development.
Area of Science:
- Gastroenterology
- Molecular Biology
- Oncology
Background:
- Colonic epithelial proliferation is normally confined to the lower crypt.
- Understanding alterations in proliferation is key to deciphering disease pathophysiology.
- Serrated polyps (SPs) represent a spectrum of colorectal lesions with potential malignant transformation.
Purpose of the Study:
- To investigate the proliferative compartment of serrated polyps using MCM2.
- To assess changes in proliferation along the serrated polyp spectrum.
- To evaluate the potential field effect in adjacent colonic mucosa.
Main Methods:
- Immunohistochemistry using an anti-MCM2 antibody.
- Analysis of normal colonic tissue, hyperplastic polyps (HPs), sessile serrated adenomas (SSAs), and SSAs with dysplasia.
- Comparison of MCM2 staining patterns across different lesion types and normal mucosa.
Main Results:
- Serrated polyps demonstrated expanded proliferative compartments compared to normal colonic crypts.
- 81.3% of HPs and 100% of SSAs showed full crypt MCM2 staining.
- Aberrant MCM2 staining in adjacent normal mucosa was observed in SSAs with dysplasia and a subset of non-dysplastic SSAs, suggesting a field effect.
Conclusions:
- Serrated polyps exhibit significant alterations in cell proliferation during their progression.
- Hyperplastic polyps and SSAs share a similar highly proliferative profile.
- The observed field effect indicates that micro-environmental changes may drive adenoma development and malignancy risk.

