Evidence map›Paper›PMID 30044991›Full record

ArticleCell reports2018

Epithelial-Mesenchymal Transition Induces Podocalyxin to Promote Extravasation via Ezrin Signaling.

Julia Fröse, Michelle B Chen, Katie E Hebron, Ferenc Reinhardt, Cynthia Hajal, Andries Zijlstra, Roger D Kamm, Robert A Weinberg

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05619159 (the Value of Immunohistochemical Expression of Moesin in Endometrial Hyperplasia and Endometrial Carcinoma), which is not on this map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 5% of its field
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.

NCT05619159 unknown statusnot on this mapstarted 2022, after this paper: background citation

the Value of Immunohistochemical Expression of Moesin in Endometrial Hyperplasia and Endometrial Carcinoma

TypeobservationalSponsorSohag UniversityRan2022 to 2023Enrolled100ConditionsEndometrial Cancer and Endometrial HyperplasiaArmsmicroscopic pathological evaluation
3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

  1. Pooled it
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  7. Ether lipids influence cancer cell fate by modulating iron uptake.bioRxiv : the preprint server for biology · 2025
    Article
  8. Inflammation awakens dormant cancer cells by modulating the epithelial-mesenchymal phenotypic state.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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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

8 authors at 5 institutions in 2 countries.

Julia FröseWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Faculty of Biosciences, University of Heidelberg, 69117 Heidelberg, Germany.
Michelle B ChenDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Katie E HebronLaboratory of Cellular and Molecular Biology, National Cancer Institute, NIH, Bethesda, MD, USA.
Ferenc ReinhardtWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Cynthia HajalDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Andries ZijlstraDepartment of Pathology, Microbiology and Immunology, Vanderbilt University, Nashville, TN 37232, USA; Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, TN 37232, USA.
Roger D KammDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA; Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.
Robert A WeinbergWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Ludwig/MIT Center for Molecular Oncology, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA. Electronic address: weinberg@wi.mit.edu.
Massachusetts Institute of Technology · USHeidelberg University · DENational Cancer Institute · USVanderbilt University · USWhitehead Institute for Biomedical Research · US

Funding

MULTIDISCIPLINARY BASIC RESEARCH TRAINING IN CANCERT32CA009592 · NCI · VANDERBILT UNIVERSITY · PI Justin M Balko, Julie A Rhoades (Sterling) · 1987 to 2026
$10.4M
Induced Differentiation to Deplete CSCs from Breast CancerR01CA078461 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI WEINBERG, ROBERT A · 1999 to 2017
$8.5M
Research Supplement - Quantitative analyses of tumor cell extravasationU01CA202177 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI KAMM, ROGER D · 2015 to 2020
$4.2M
High-throughput palmitoyl-proteomics profiling of extracellular vesicles for identification of biomarkers for early detection of clinically significant prostate cancerR01CA218526 · NCI · CEDARS-SINAI MEDICAL CENTER · PI DI VIZIO, DOLORES, HURLEY, PAULA JILL · 2017 to 2021
$2.0M
Regulation of prostate cancer progression by ALCAM proteolysisF31CA189764 · NCI · VANDERBILT UNIVERSITY · PI HEBRON, KATIE ELIZABETH · 2014 to 2016
$76k
NCI NIH HHS F31 CA189764NCI NIH HHS R01 CA078461NCI NIH HHS R01 CA218526NCI NIH HHS T32 CA009592NCI NIH HHS U01 CA202177
6 · The paper itself

Abstract

The epithelial-mesenchymal transition (EMT) endows carcinoma cells with traits needed to complete many of the steps leading to metastasis formation, but its contributions specifically to the late step of extravasation remain understudied. We find that breast cancer cells that have undergone an EMT extravasate more efficiently from blood vessels both in vitro and in vivo. Analysis of gene expression changes associated with the EMT program led to the identification of an EMT-induced cell-surface protein, podocalyxin (PODXL), as a key mediator of extravasation in mesenchymal breast and pancreatic carcinoma cells. PODXL promotes extravasation through direct interaction of its intracellular domain with the cytoskeletal linker protein ezrin. Ezrin proceeds to establish dorsal cortical polarity, enabling the transition of cancer cells from a non-polarized, rounded cell morphology to an invasive extravasation-competent shape. Hence, the EMT program can directly enhance the efficiency of extravasation and subsequent metastasis formation through a PODXL-ezrin signaling axis.

Indexed as

AnimalsBreast NeoplasmsCell Line, TumorCytoskeletal ProteinsEpithelial-Mesenchymal TransitionEzrinFemaleHeterograftsHumansLung NeoplasmsMaleMiceMice, Inbred NODMice, SCIDPancreatic NeoplasmsSialoglycoproteinsCytoskeletal ProteinsEzrinpodocalyxinSialoglycoproteinsEMTextravasationezrinmetastasisPODXL

Identifiers

PMID30044991
PMCPMC6181240
OpenAlexW2882986891

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.