Published online Jun 7, 2021. doi: 10.3748/wjg.v27.i21.2710
Peer-review started: January 17, 2021
First decision: February 9, 2021
Revised: February 25, 2021
Accepted: April 14, 2021
Article in press: April 14, 2021
Published online: June 7, 2021
Processing time: 129 Days and 16.4 Hours
Genetic alterations in pancreatic tumors can usually be classified in: (1) Mutational activation of oncogenes; (2) Inactivation of tumor suppressor genes; and (3) Inactivation of genome maintenance genes controlling the repair of DNA damage. Endoscopic ultrasound-guided fine-needle aspiration has improved pre-operative diagnosis, but the management of patients with a pancreatic lesion is still challenging. Molecular testing could help mainly in solving these “inconclusive” specimens. The introduction of multi-gene analysis approaches, such as next-generation sequencing, has provided a lot of useful information on the molecular characterization of pancreatic tumors. Different types of pancreatic tumors (e.g., pancreatic ductal adenocarcinomas, intraductal papillary mucinous neoplasms, solid pseudopapillary tumors) are characterized by specific molecular alterations. The aim of this review is to summarize the main molecular alterations found in pancreatic tumors.
Core Tip: To date, in patients with pancreatic cancer there are no targetable molecules for personalized treatment in clinical practice. The introduction of multi-gene analysis approaches, such as massive parallel sequencing, has provided a lot of useful information regarding the molecular characterization of pancreatic tumors. However, a huge amount of data needs to be properly managed to determine the information that is useful and correct. A deeper knowledge of the molecular alterations characterizing pancreatic neoplasms may lead to new potential therapeutic targets for these tumors.