Evidence map›Paper›PMID 32381732›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

A mode of cell adhesion and migration facilitated by CD44-dependent microtentacles.

Kayla J Wolf, Poojan Shukla, Kelsey Springer, Stacey Lee, Jason D Coombes, Caleb J Choy, Samuel J Kenny, Ke Xu, Sanjay Kumar

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
6.5field-weighted citation impact, top 2% 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.

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

68 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
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  7. Decoding Rho GTPase signalling networks in directed cell migration.Frontiers in cell and developmental biology · 2026
    Review
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  16. Microenvironmental Drivers of Glioma Progression.International journal of molecular sciences · 2025
    Review
  17. Article
  18. Article
  19. Article
  20. Article

8 more citing papers are in PubMed but not listed here.

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

9 authors at 4 institutions in 2 countries.

Kayla J WolfUniversity of California, Berkeley-University of California San Francisco Graduate Program in Bioengineering, Department of Bioengineering, University of California, Berkeley, CA 94720.ORCID 0000-0001-6990-0283
Poojan ShuklaDepartment of Bioengineering, University of California, Berkeley, CA, 94720.
Kelsey SpringerDepartment of Bioengineering, University of California, Berkeley, CA, 94720.
Stacey LeeUniversity of California, Berkeley-University of California San Francisco Graduate Program in Bioengineering, Department of Bioengineering, University of California, Berkeley, CA 94720.
Jason D CoombesDepartment of Bioengineering, University of California, Berkeley, CA, 94720.
Caleb J ChoyDepartment of Molecular and Cell Biology, University of California, Berkeley, CA 94720.
Samuel J KennyDepartment of Chemistry, University of California, Berkeley, CA 94720.
Ke XuDepartment of Chemistry, University of California, Berkeley, CA 94720.ORCID 0000-0002-2788-194X
Sanjay KumarUniversity of California, Berkeley-University of California San Francisco Graduate Program in Bioengineering, Department of Bioengineering, University of California, Berkeley, CA 94720; skumar@berkeley.edu.ORCID 0000-0002-9996-4883
University of California, Berkeley · USUniversity of California, San Francisco · USKing's College London · GBLawrence Berkeley National Laboratory · US

Funding

Biophysical Control of Cell Form and Function by Single Actomyosin Stress Fibers: Instrument SupplementR01GM122375 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI KUMAR, SANJAY · 2017 to 2025
$2.7M
Modeling and druggable-genome screening of glioblastoma invasion using regional biopsy-guided biomaterials systemsR01CA227136 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AGHI, MANISH · 2018 to 2022
$2.2M
Molecular analysis of physical microenvironmental control of tumor cell invasionR21CA174573 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI KUMAR, SANJAY · 2014 to 2016
$655k
A Zeiss Elyra S1 Structured Illumination Microscope for the Biological Imaging FaS10OD018136 · OD · UNIVERSITY OF CALIFORNIA BERKELEY · PI RUZIN, STEVEN EARL · 2014 to 2014
$600k
Genetic strategies for the quantitative control of cell-matrix mechanobiologyR21EB016359 · NIBIB · UNIVERSITY OF CALIFORNIA BERKELEY · PI KUMAR, SANJAY · 2013 to 2014
$425k
High-throughput Analysis of MicroRNA Regulation of Stem Cell MechanobiologyR21EB025017 · NIBIB · UNIVERSITY OF CALIFORNIA BERKELEY · PI KUMAR, SANJAY · 2017 to 2018
$411k
Mechanical Regulation of Cell Shape and Migration by Actin Stress Fiber SubpopulationsF31GM119329 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI LEE, STACEY · 2017 to 2018
$78k
A 3D Model of the Perivascular Niche to Investigate Glioblastoma InvasionF31CA228317 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI WOLF, KAYLA · 2018 to 2019
$74k
NCI NIH HHS F31 CA228317NCI NIH HHS R01 CA227136NCI NIH HHS R21 CA174573NIBIB NIH HHS R21 EB016359NIBIB NIH HHS R21 EB025017NIGMS NIH HHS F31 GM119329NIGMS NIH HHS R01 GM122375NIH HHS S10 OD018136
6 · The paper itself

Abstract

The structure and mechanics of many connective tissues are dictated by a collagen-rich extracellular matrix (ECM), where collagen fibers provide topological cues that direct cell migration. However, comparatively little is known about how cells navigate the hyaluronic acid (HA)-rich, nanoporous ECM of the brain, a problem with fundamental implications for development, inflammation, and tumor invasion. Here, we demonstrate that glioblastoma cells adhere to and invade HA-rich matrix using microtentacles (McTNs), which extend tens of micrometers from the cell body and are distinct from filopodia. We observe these structures in continuous culture models and primary patient-derived tumor cells, as well as in synthetic HA matrix and organotypic brain slices. High-magnification and superresolution imaging reveals McTNs are dynamic, CD44-coated tubular protrusions containing microtubules and actin filaments, which respectively drive McTN extension and retraction. Molecular mechanistic studies reveal that McTNs are stabilized by an interplay between microtubule-driven protrusion, actomyosin-driven retraction, and CD44-mediated adhesion, where adhesive and cytoskeletal components are mechanistically coupled by an IQGAP1-CLIP170 complex. McTNs represent a previously unappreciated mechanism through which cells engage nanoporous HA matrix and may represent an important molecular target in physiology and disease.

Indexed as

ActinsAnimalsBrainCell AdhesionCell Line, TumorCell MovementExtracellular MatrixFemaleGene Knockout TechniquesGlioblastomaHumansHyaluronan ReceptorsHyaluronic AcidMiceMicrotubule-Associated ProteinsMicrotubulesActinsarginyl-glycyl-aspartic acidCD44 protein, humancytoplasmic linker protein 170Hyaluronan ReceptorsHyaluronic AcidIQ motif containing GTPase activating protein 1Microtubule-Associated ProteinsMYO10 protein, humanMyosinsNeoplasm ProteinsOligopeptidesras GTPase-Activating Proteinsextracellular matrixglioblastomahyaluronic acidmechanobiologymotility

Identifiers

PMID32381732
PMCPMC7261014
OpenAlexW3023282059

What OpenQuestion holds

Textmetadata
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.