Unknown

Dataset Information

0

Cancer Cells Retrace a Stepwise Differentiation Program during Malignant Progression.


ABSTRACT: Pancreatic neuroendocrine tumors (PanNET) comprise two molecular subtypes, relatively benign islet tumors (IT) and invasive, metastasis-like primary (MLP) tumors. Until now, the origin of aggressive MLP tumors has been obscure. Herein, using multi-omics approaches, we revealed that MLP tumors arise from IT via dedifferentiation following a reverse trajectory along the developmental pathway of islet β cells, which results in the acquisition of a progenitor-like molecular phenotype. Functionally, the miR-181cd cluster induces the IT-to-MLP transition by suppressing expression of the Meis2 transcription factor, leading to upregulation of a developmental transcription factor, Hmgb3. Notably, the IT-to-MLP transition constitutes a distinct step of tumorigenesis and is separable from the classic proliferation-associated hallmark, temporally preceding accelerated proliferation of cancer cells. Furthermore, patients with PanNET with elevated HMGB3 expression and an MLP transcriptional signature are associated with higher-grade tumors and worse survival. Overall, our results unveil a new mechanism that modulates cancer cell plasticity to enable malignant progression. SIGNIFICANCE: Dedifferentiation has long been observed as a histopathologic characteristic of many cancers, albeit inseparable from concurrent increases in cell proliferation. Herein, we demonstrate that dedifferentiation is a mechanistically and temporally separable step in the multistage tumorigenesis of pancreatic islet cells, retracing the developmental lineage of islet β cells.This article is highlighted in the In This Issue feature, p. 2355.

SUBMITTER: Saghafinia S 

PROVIDER: S-EPMC7611766 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC3277591 | biostudies-literature
| S-EPMC6439469 | biostudies-literature
| S-EPMC5777712 | biostudies-literature
2018-08-21 | PXD009868 | Pride
| S-EPMC3738969 | biostudies-literature
| S-EPMC5520915 | biostudies-literature
| S-EPMC3427728 | biostudies-literature
| S-EPMC8692003 | biostudies-literature
| S-EPMC3208563 | biostudies-literature
| S-EPMC7017725 | biostudies-literature