Evidence map›Paper›PMID 32086369›Full record

ArticleMolecular cancer research : MCR2020

Cdc42 Mediates Cancer Cell Chemotaxis in Perineural Invasion.

Natalya Chernichenko, Tatiana Omelchenko, Sylvie Deborde, Richard L Bakst, Shizhi He, Chun-Hao Chen, Laxmi Gusain, Efsevia Vakiani, Nora Katabi, Alan Hall and 1 more

Abstract read
In one paragraph

Article in Molecular cancer research : MCR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
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  8. Review
  9. Review
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  11. Rapid cancer cell perineural invasion utilizes amoeboid migration.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. Article
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  16. Review
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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

11 authors.

Natalya ChernichenkoDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York.
Tatiana OmelchenkoCell Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York.
Sylvie DebordeDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York.
Richard L BakstDepartment of Radiation Oncology, Mount Sinai Hospital, New York, New York.
Shizhi HeDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York.
Chun-Hao ChenDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York.
Laxmi GusainDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York.ORCID 0000-0002-7140-5350
Efsevia VakianiDepartment of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York.
Nora KatabiDepartment of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York.
Alan HallCell Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York.
Richard J WongDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York. wongr@mskcc.org.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
HEAD AND NECK TRAINING PROGRAM SURGICAL ONCOLOGYT32CA009685 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI FAGIN, JAMES A, WONG, RICHARD J · 1992 to 2022
$3.6M
Schwann Cell Reprogramming and Cancer Perineural InvasionR01CA219534 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI WONG, RICHARD J · 2017 to 2021
$3.1M
Mechanisms of cancer cell chemotaxis in perineural invasionR01CA157686 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI WONG, RICHARD J · 2011 to 2015
$1.9M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA157686NCI NIH HHS R01 CA219534NCI NIH HHS T32 CA009685
6 · The paper itself

Abstract

Perineural invasion (PNI) is an ominous form of cancer progression along nerves associated with poor clinical outcome. Glial derived neurotrophic factor (GDNF) interacts with cancer cell RET receptors to enable PNI, but downstream events remain undefined. We demonstrate that GDNF leads to early activation of the GTPase Cdc42 in pancreatic cancer cells, but only delayed activation of RhoA and does not affect Rac1. Depletion of Cdc42 impairs pancreatic cancer cell chemotaxis toward GDNF and nerves. An siRNA library of guanine nucleotide exchange factors was screened to identify activators of Cdc42. ARHGEF7 (β-Pix) was required for Cdc42 activation and chemotaxis toward nerves, and also colocalizes with RET under GDNF stimulation. Cdc42 enables PNI in an

Indexed as

Cell MovementAnimalsApoptosiscdc42 GTP-Binding ProteinCell ProliferationFemaleGlial Cell Line-Derived Neurotrophic FactorHumansMiceMice, NudeNeoplasm InvasivenessPancreatic NeoplasmsRho Guanine Nucleotide Exchange FactorsSciatic NerveTumor Cells, CulturedXenograft Model Antitumor AssaysARHGEF7 protein, humancdc42 GTP-Binding ProteinCDC42 protein, humanGDNF protein, humanGlial Cell Line-Derived Neurotrophic FactorRho Guanine Nucleotide Exchange Factors

Identifiers

PMID32086369
PMCPMC7272295

What OpenQuestion holds

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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.