Evidence map›Paper›PMID 32665556›Full record

ArticleNature communications2020

In vivo microscopy reveals macrophage polarization locally promotes coherent microtubule dynamics in migrating cancer cells.

Gaurav Luthria, Ran Li, Stephanie Wang, Mark Prytyskach, Rainer H Kohler, Douglas A Lauffenburger, Timothy J Mitchison, Ralph Weissleder, Miles A Miller

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  4. Thyroid Cancers Exhibit Oncogene-Enhanced Macropinocytosis that Is Restrained by IGF1R and Promote Albumin-Drug Conjugate Response.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
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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

9 authors at 3 institutions in 1 country.

Gaurav LuthriaCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, 02114, USA.ORCID http://orcid.org/0000-0002-7896-6134
Ran LiCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, 02114, USA.ORCID http://orcid.org/0000-0002-8537-8824
Stephanie WangDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02181, USA.
Mark PrytyskachCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, 02114, USA.
Rainer H KohlerCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, 02114, USA.ORCID http://orcid.org/0000-0001-6269-6590
Douglas A LauffenburgerDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02181, USA.ORCID http://orcid.org/0000-0002-0050-989X
Timothy J MitchisonDepartment of Systems Biology, Harvard Medical School, Boston, MA, 02115, USA.
Ralph WeisslederCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, 02114, USA. rweissleder@mgh.harvard.edu.ORCID http://orcid.org/0000-0003-0828-4143
Miles A MillerCenter for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, 02114, USA. miles.miller@mgh.harvard.edu.ORCID http://orcid.org/0000-0001-7638-8898
Harvard University · USMassachusetts General Hospital · USMassachusetts Institute of Technology · US

Funding

Tumor Cell Networks CenterU54CA112967 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LAUFFENBURGER, DOUGLAS A · 2004 to 2015
$26.2M
Training Program in Bioinformatics and Integrative GenomicsT32HG002295 · NHGRI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Peter J Park · 2001 to 2026
$15.8M
Quantitative and functional characterization of therapeutic resistance in cancerU54CA217377 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LAUFFENBURGER, DOUGLAS A, MANALIS, SCOTT R · 2017 to 2021
$10.2M
Training Grant in Molecular Imaging Research (MGH/HMS)T32CA079443 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, MD, PHD, RALPH · 2000 to 2025
$10.1M
Engineered Antibody EGFR Antagonist Cancer TherapeuticsR01CA096504 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI WITTRUP, KARL DANE · 2002 to 2017
$9.7M
Spatial Segregation of Cell Functioning During MotilityR01GM069668 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WELLS, ALAN · 2004 to 2019
$4.7M
Imaging of nanotherapeutic drug actionU01CA206997 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, MD, PHD, RALPH · 2017 to 2021
$2.9M
Imaging tumor associated macrophage (TAM) functionR01CA206890 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI PITTET, MIKAEL, WEISSLEDER, MD, PHD, RALPH · 2017 to 2021
$1.9M
Single Cell In Vivo Imaging Technology to Analyze Taxane Nano Formulations in Breast CancerR00CA207744 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI MILLER, MILES A · 2018 to 2020
$747k
NCI NIH HHS R00 CA207744NCI NIH HHS R01 CA096504NCI NIH HHS R01 CA206890NCI NIH HHS T32 CA079443NCI NIH HHS U01 CA206997NCI NIH HHS U54 CA112967NCI NIH HHS U54 CA217377NHGRI NIH HHS T32 HG002295NIGMS NIH HHS R01 GM069668
6 · The paper itself

Abstract

Microtubules (MTs) mediate mitosis, directional signaling, and are therapeutic targets in cancer. Yet in vivo analysis of cancer cell MT behavior within the tumor microenvironment remains challenging. Here we developed an imaging pipeline using plus-end tip tracking and intravital microscopy to quantify MT dynamics in live xenograft tumor models. Among analyzed features, cancer cells in vivo displayed higher coherent orientation of MT dynamics along their cell major axes compared with 2D in vitro cultures, and distinct from 3D collagen gel cultures. This in vivo MT phenotype was reproduced in vitro when cells were co-cultured with IL4-polarized MΦ. MΦ depletion, MT disruption, targeted kinase inhibition, and altered MΦ polarization via IL10R blockade all reduced MT coherence and/or tumor cell elongation. We show that MT coherence is a defining feature for in vivo tumor cell dynamics and migration, modulated by local signaling from pro-tumor macrophages.

Indexed as

AnimalsCell CycleCell MovementFemaleHumansMacrophagesMiceMicrotubule-Associated ProteinsMicrotubulesMitosisPrincipal Component AnalysisRAW 264.7 CellsMicrotubule-Associated Proteins

Identifiers

PMID32665556
PMCPMC7360550
OpenAlexW3042781060

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.