Published online May 21, 2023. doi: 10.3748/wjg.v29.i19.2961
Peer-review started: February 28, 2023
First decision: March 14, 2023
Revised: March 24, 2023
Accepted: April 23, 2023
Article in press: April 23, 2023
Published online: May 21, 2023
Processing time: 76 Days and 24 Hours
Intrahepatic cholangiocarcinoma (ICC) has a high mortality rate. Its early diagnosis is very important.
At present, there are no diagnostic markers of ICC, and most patients are in the middle and late stage when the tumors are found, and the treatment options for these patients are limited, resulting in a poor prognosis.
It is urgent to find new biomarkers for early screening and diagnosis of ICC.
Bioinformatics analysis and machine learning algorithm were used to screen for ICC disease characteristic genes, and the diagnostic performance of characteristic gene MMP14 was verified by different databases. The relationship between different immune cell infiltration in MMP14 and ICC tumor microenvironment was analyzed.
We discovered for the first time a new gene MMP14 for the diagnosis of ICC. We further analyzed the expression of MMP14 and its significance in immune cell infiltration in ICC tumor microenvironment, indicating that MMP14 is closely related to a variety of immune cell infiltration, which may provide a new direction for immune-related research.
In this study, we found that MMP14 can be used as a disease characteristic gene for ICC diagnosis using a variety of machine learning algorithms. There is a relationship between different immune cell infiltration in MMP14 and ICC tumor microenvironment, which plays an important role in the occurrence and development of tumor. MMP14 may be a potential target for ICC immunotherapy.
Based on bioinformatics analysis and machine learning algorithm, MMP14 was identified as the characteristic gene of ICC and was associated with ICC immune cell infiltration. In the future research, it will be of great significance to explore the signal pathway mediated by MMP14 in the occurrence and development of ICC and the mechanism of immune cell infiltration.
