Published online Jul 7, 2021. doi: 10.3748/wjg.v27.i25.3888
Peer-review started: January 29, 2021
First decision: February 25, 2021
Revised: March 11, 2021
Accepted: June 4, 2021
Article in press: June 4, 2021
Published online: July 7, 2021
Processing time: 157 Days and 23.9 Hours
At present, several studies have reported abnormal expression patterns of mucin 2 (MUC2) in cancerous lesions, including colorectal cancer (CRC). However, as a member of the intestinal mucosal mechanical barrier, the relationship between MUC2 and the intestinal mucosal barrier in patients with CRC remains unclear. Revealing this association will help us more fully understand the role of MUC2 in CRC.
Although many studies have proved that intestinal mucosal barrier function is impair
This study aimed to explore abnormal expression patterns of MUC2 and the rela
Immunohistochemical staining was performed on cancer tissue and normal tissue samples from 100 patients with CRC to evaluate the expression of MUC2 in two different tissues, and these patients were followed for 12-60 mo to understand the overall survival (OS) and disease-free survival (DFS). Preoperative serum levels of MUC2, diamine oxide (DAO), and D-lactate (D-LAC) in 66 patients with CRC were detected by enzyme-linked immunosorbent assay and compared with those in 20 normal controls, so as to evaluate the damage of intestinal mucosal barrier in patients with CRC. The statistical methods involved in this study include χ2 test, Fisher’s exact test, Kaplan-Meier curve, and log-rank tests.
Immunohistochemical staining results showed that the expression of MUC2 in cancer tissues was lower than that in normal tissues (54% vs 79%, P < 0.05), and the expression of MUC2 was correlated with tumor-node-metastasis (TNM) stage and lymph node metastasis in CRC patients (P < 0.05), but not significantly related to the patient’s age, sex, tumor location, size, depth of invasion, or degree of differentiation. The serum levels of MUC2, DAO, and D-LAC in patients with CRC were higher than those in normal people (P < 0.05), and were positively associated with serum levels of human DAO (χ2 = 3.957, P < 0.05) and D-LAC (χ2 = 7.236, P < 0.05), which are the biomarkers of the functional status of the intestinal mucosal barriers. It was suggested that the intestinal mucosal barrier was damaged, and MUC2 can also be used as a new evaluation index. The serum levels of MUC2 were correlated with TNM stage, tumor type, and distant metastasis in CRC patients (P < 0.05). It seems to be a trend that patients with higher malignancy and later stage of tumors have higher serum MUC2 levels. Survival analysis showed that decreased expression of MUC2 in CRC tissues predicted a poor survival. The expression of MUC2 in tissues was significantly correlated with DFS (P = 0.032) and OS (P = 0.037). And the recurrence rate of patients with low expression of MUC2 was higher than that of patients with high expression of MUC2 (40% vs 18.5%, χ2 = 5.485, P < 0.05).
MUC2 in the intestinal tissue may play a protective role on the intestine, which can be used as an indicator to evaluate the prognosis of CRC patients. Intestinal mucosal barrier function of CRC patients is impaired, and the serum MUC2 level can reflect the severity of the damage.
Future researchers can further study the molecular mechanism of MUC2 in the process of intestinal mucosal barrier damage, which may reveal the pathological mechanism of CRC from a new perspective and provide a basis for the development of new targeted therapy drugs. In addition, related research can also be carried out in inflammatory bowel disease.