Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Oct 22:9:28.
doi: 10.1186/s40164-020-00184-0. eCollection 2020.

Molecular drivers and cells of origin in pancreatic ductal adenocarcinoma and pancreatic neuroendocrine carcinoma

Affiliations
Review

Molecular drivers and cells of origin in pancreatic ductal adenocarcinoma and pancreatic neuroendocrine carcinoma

He-Li Gao et al. Exp Hematol Oncol. .

Abstract

Pancreatic cancer is one of the most common causes of cancer-related deaths worldwide. The two major histological subtypes of pancreatic cancer are pancreatic ductal adenocarcinoma (PDAC), accounting for 90% of all cases, and pancreatic neuroendocrine neoplasm (PanNEN), which makes up 3-5% of all cases. PanNEN is classified into well-differentiated pancreatic neuroendocrine tumor and poorly-differentiated pancreatic neuroendocrine carcinoma (PanNEC). Although PDAC and PanNEN are commonly thought to be different diseases with distinct biology, cell of origin, and genomic abnormalities, the idea that PDAC and PanNEC share common cells of origin has been gaining support. This is substantiated by evidence that the molecular profiling of PanNEC is genetically and phenotypically related to PDAC. In the current review, we summarize published studies pointing to common potential cells of origin and speculate about how the distinct paths of differentiation are determined by the genomic patterns of each disease. We also discuss the overlap between PDAC and PanNEC, which has been noted in clinical observations.

Keywords: Carcinogenesis; Genomic patterns; Neuroendocrine tumor; Pancreatic adenocarcinoma; Pancreatic neuroendocrine carcinoma.

PubMed Disclaimer

Conflict of interest statement

Competing interestsThe authors have no conflicts of interest to declare.

Figures

Fig. 1
Fig. 1
Endocrine and exocrine cell differentiation during pancreas development
Fig. 2
Fig. 2
Driver gene association network between PanNET (a) and PDAC (b)
Fig. 3
Fig. 3
Hypothesis of the evolution of PanNET, PDAC, and PanNET cells of origin

Similar articles

Cited by

References

    1. Siegel RL, et al. Cancer statistics, 2020. CA Cancer J Clin. 2020;70(1):7–30. doi: 10.3322/caac.21590. - DOI - PubMed
    1. Christenson ES, et al. Current and emerging therapies for patients with advanced pancreatic ductal adenocarcinoma: a bright future. Lancet Oncol. 2020;21(3):e135–e145. doi: 10.1016/S1470-2045(19)30795-8. - DOI - PMC - PubMed
    1. Makohon-Moore A, et al. Pancreatic cancer biology and genetics from an evolutionary perspective. Nat Rev Cancer. 2016;16(9):553–565. doi: 10.1038/nrc.2016.66. - DOI - PMC - PubMed
    1. Cives M, et al. Gastroenteropancreatic Neuroendocrine Tumors. CA Cancer J Clin. 2018;68(6):471–487. doi: 10.3322/caac.21493. - DOI - PubMed
    1. Sorbye H, et al. Gastroenteropancreatic high-grade neuroendocrine carcinoma. Cancer. 2014;120(18):2814–2823. doi: 10.1002/cncr.28721. - DOI - PubMed

LinkOut - more resources