Published online Dec 21, 2017. doi: 10.3748/wjg.v23.i47.8367
Peer-review started: October 26, 2017
First decision: November 21, 2017
Revised: November 30, 2017
Accepted: December 4, 2017
Article in press: December 4, 2017
Published online: December 21, 2017
Processing time: 55 Days and 17.9 Hours
White opaque substance (WOS) under magnifying narrow-band imaging (M-NBI) endoscopy is a novel endoscopic finding for the diagnosis of gastrointestinal tract neoplasms. In previous studies, WOS has been shown to contain lipid droplets. However, the association between the distribution of the lipid droplets and endoscopically verified WOS in colorectal neoplasms remains unclear.
The elucidation of WOS or lipid droplets in colorectal epithelial tumors will help the diagnosis and treatment of colorectal epithelial tumors.
To examine the association between WOS and histologically verified lipid droplets in colorectal epithelial neoplasms.
We conducted this retrospective study involving 129 lesions of endoscopically or surgically resected colorectal epithelial neoplasms observed by M-NBI colonoscopy. Immunohistochemistry was used to stain tumors with a monoclonal antibody specific to adipophilin as a marker of lipids. The expression and distribution of adipophilin were compared between WOS-positive and WOS-negative lesions and among tumors classified by histologic type and depth of invasion.
81 lesions were positive for WOS and 48 lesions were negative for WOS. The rate of adipophilin expression was significantly higher in WOS-positive lesions (95.1%) than in WOS-negative lesions (68.7%) (P = 0.0001). The incidence of deep adipophilin expression was higher in WOS-positive lesions (24.7%) than in WOS-negative lesions (4.2%) (P = 0.001). The incidence of deep expression was predominant among cancers with massive submucosal invasion (62.5%) compared to adenoma (7.2%) and high-grade dysplasia or cancers with slight submucosal invasion (12.7%) (P = 0.0001).
The distribution of lipid droplets may be closely associated with the visibility of WOS under M-NBI colonoscopy, and with histologic grade and depth of tumor invasion.
Our study showed that WOS under M-NBI colonoscopy appears to represent lipid droplets and the distribution of lipid droplets may be closely associated with the visibility of WOS with histologic grade and depth of tumor invasion. The accumulation of lipid droplets may directly or indirectly represent the malignant potential of colon cancer cells. Further prospective studies are warranted to establish the clinical significance of WOS for the diagnosis and treatment of colorectal epithelial tumors and the association between lipid droplets and WOS under NBI.
