Evidence map›Paper›PMID 40493403›Full record

ArticleJCI insight2025

Emerin is an effector of oncogenic KRAS-driven nuclear dynamics in pancreatic cancer.

Luis F Flores, David L Marks, Renzo E Vera, Ashley N Sigafoos, Ezequiel J Tolosa, Luciana L Almada, David R Pease, Merih D Toruner, Brian Chang, Brooke R Tader and 11 more

Abstract read
In one paragraph

Article in JCI insight, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Luis F FloresDivision of Oncology Research.
David L MarksDivision of Oncology Research.
Renzo E VeraDivision of Oncology Research.
Ashley N SigafoosDivision of Oncology Research.
Ezequiel J TolosaDivision of Oncology Research.
Luciana L AlmadaDivision of Oncology Research.
David R PeaseDivision of Oncology Research.
Merih D TorunerDivision of Oncology Research.
Brian ChangDivision of Oncology Research.
Brooke R TaderDivision of Oncology Research.
Kayla C LaRue-NolanDivision of Oncology Research.
Ryan M CarrDivision of Oncology Research.
Rondell P GrahamDivision of Anatomic Pathology, Department of Laboratory Medicine and Pathology, and.
Catherine E HagenDivision of Anatomic Pathology, Department of Laboratory Medicine and Pathology, and.
Matthew R BrownDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota, USA.
Aleksey V MatveyenkoDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota, USA.
Katherine L WilsonDepartment of Cell Biology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
David W DawsonDepartment of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
Christopher L PinDepartments of Physiology and Pharmacology, Oncology, and Pediatrics, Schulich School of Medicine, University of Western Ontario, Verspeeten Family Cancer Centre, London, Ontario, Canada.
Kyle J RouxSanford Research, Enabling Technologies Group, Sioux Falls, South Dakota, USA.
Martin E Fernandez-ZapicoDivision of Oncology Research.

Funding

Mechanism of Pancreatic CarcinogenesisR01CA136526 · NCI · MAYO CLINIC ROCHESTER · PI FERNANDEZ-ZAPICO, MARTIN ERNESTO · 2009 to 2019
$3.0M
New Therapuetics for Pancreatic CancerR01CA265050 · NCI · MAYO CLINIC ROCHESTER · PI Mitesh Borad, Martin Ernesto Fernandez-Zapico · 2022 to 2026
$3.0M
Mechanisms of gene expression regulation in pancreatic cancerK00CA284259 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI David R Pease · 2024 to 2026
$324k
Mechanisms of gene expression regulation in pancreatic cancerF99CA284259 · NCI · MAYO CLINIC ROCHESTER · PI PEASE, DAVID R · 2023 to 2024
$98k
NCI NIH HHS F99 CA284259NCI NIH HHS K00 CA284259NCI NIH HHS R01 CA136526NCI NIH HHS R01 CA265050
6 · The paper itself

Abstract

For over a century, scientists reported the disruption of normal nuclear shape and size in cancer. These changes have long been used as tools for diagnosis and staging of malignancies. However, to date, the mechanisms underlying these aberrant nuclear phenotypes and their biological significance remain poorly understood. Using a model of pancreatic ductal adenocarcinoma (PDAC), the major histological subtypes of pancreatic cancer, we found that oncogenic mutant KRAS reduces nuclear size. Transcriptomic and protein expression analysis of mutant KRAS-expressing PDAC cells revealed differential levels of several nuclear envelope-associated genes. Further analysis demonstrated the nuclear lamina protein, Emerin (EMD), acted downstream of KRAS to mediate nuclear size reduction in PDAC. Analysis of human PDAC samples showed that increased EMD expression associates with reduced nuclear size. Finally, in vivo genetic depletion of EMD in a mutant KRAS-driven PDAC model resulted in increased nuclear size and a reduced incidence of poorly differentiated PDAC. Thus, our data provide evidence of a potentially novel mechanism underlying nuclear size regulation and its effect in PDAC carcinogenesis.

Indexed as

Carcinoma, Pancreatic DuctalCell NucleusMembrane ProteinsNuclear ProteinsPancreatic NeoplasmsProto-Oncogene Proteins p21(ras)AnimalsCell Line, TumorGene Expression Regulation, NeoplasticHumansMiceMutationemerinKRAS protein, humanMembrane ProteinsNuclear ProteinsProto-Oncogene Proteins p21(ras)CancerCell biologyOncology

Identifiers

PMID40493403
PMCPMC12288966

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.