Published online Sep 28, 2021. doi: 10.3748/wjg.v27.i36.6004
Peer-review started: January 27, 2021
First decision: February 25, 2021
Revised: March 12, 2021
Accepted: April 22, 2021
Article in press: April 22, 2021
Published online: September 28, 2021
Processing time: 238 Days and 18.6 Hours
Pancreatic cancer (PC) is an aggressive human cancer. Appropriate methods for the diagnosis and treatment of PC have not been found at the genetic level, thus making epigenetics a promising research path in studies of PC. Histone methylation is one of the most complicated types of epigenetic modifications and has proved crucial in the development of PC. Histone methylation is a reversible process regulated by readers, writers, and erasers. Some writers and erasers can be recognized as potential biomarkers and candidate therapeutic targets in PC because of their unusual expression in PC cells compared with normal pancreatic cells. Based on the impact that writers have on the development of PC, some inhibitors of writers have been developed. However, few inhibitors of erasers have been developed and put to clinical use. Meanwhile, there is not enough research on the reader domains. Therefore, the study of erasers and readers is still a promising area. This review focuses on the regulatory mechanism of histone methylation, and the diagnosis and chemotherapy of PC based on it. The future of epigenetic modification in PC research is also discussed.
Core Tip: Pancreatic cancer is a highly lethal malignancy of the digestive tract that is difficult to diagnose and treat. Histone methylation/demethylation equilibrium is altered in carcinogenesis, resulting in changes in chromatin structure and gene expression. Not only are histone methylation writers related to histone methylation erasers but histone methylation is also related to other epigenetic modifications. Therefore, histone methylation is addressed as a potentially important chemotherapy drug target.