Evidence map›Paper›PMID 24552821›Full record

ArticleCell cycle (Georgetown, Tex.)2014

Invading cancer cells are predominantly in G0/G1 resulting in chemoresistance demonstrated by real-time FUCCI imaging.

Shuya Yano, Shinji Miwa, Sumiyuki Mii, Yukihiko Hiroshima, Fuminari Uehara, Mako Yamamoto, Hiroyuki Kishimoto, Hiroshi Tazawa, Michael Bouvet, Toshiyoshi Fujiwara and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
7.8field-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

47 citing papers in PubMed, 78 citations in OpenAlex.

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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 at 4 institutions in 2 countries.

Shuya YanoAntiCancer, Inc; San Diego, CA USA; Department of Surgery; University of California, San Diego; San Diego, CA USA; Department of Gastroenterological Surgery; Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences; Okayama, Japan.
Shinji MiwaAntiCancer, Inc; San Diego, CA USA; Department of Surgery; University of California, San Diego; San Diego, CA USA.
Sumiyuki MiiAntiCancer, Inc; San Diego, CA USA; Department of Surgery; University of California, San Diego; San Diego, CA USA.
Yukihiko HiroshimaAntiCancer, Inc; San Diego, CA USA; Department of Surgery; University of California, San Diego; San Diego, CA USA.
Fuminari UeharaAntiCancer, Inc; San Diego, CA USA; Department of Surgery; University of California, San Diego; San Diego, CA USA.
Mako YamamotoAntiCancer, Inc; San Diego, CA USA; Department of Surgery; University of California, San Diego; San Diego, CA USA.
Hiroyuki KishimotoDepartment of Gastroenterological Surgery; Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences; Okayama, Japan.
Hiroshi TazawaCenter for Innovative Clinical Medicine; Okayama University Hospital; Okayama, Japan.
Michael BouvetDepartment of Surgery; University of California, San Diego; San Diego, CA USA.
Toshiyoshi FujiwaraDepartment of Gastroenterological Surgery; Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences; Okayama, Japan.
Robert M HoffmanAntiCancer, Inc; San Diego, CA USA; Department of Surgery; University of California, San Diego; San Diego, CA USA.
University of California, San Diego · USOkayama University · JPAntiCancer (United States) · USInnovative Clinical Research · US

Funding

Color-Coded Imaging of Pancreatic Cancer Microenvironment for Drug DiscoveryR01CA132971 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BOUVET, MICHAEL, YANG, MENG · 2009 to 2013
$1.7M
NCI NIH HHS CA132971NCI NIH HHS R01 CA132971
6 · The paper itself

Abstract

Invasive cancer cells are a critical target in order to prevent metastasis. In the present report, we demonstrate real-time visualization of cell cycle kinetics of invading cancer cells in 3-dimensional (3D) Gelfoam® histoculture, which is in vivo-like. A fluorescence ubiquitination cell cycle indicator (FUCCI) whereby G0/G1 cells express a red fluorescent protein and S/G2/M cells express a green fluorescent protein was used to determine the cell cycle position of invading and non-invading cells. With FUCCI 3D confocal imaging, we observed that cancer cells in G0/G1 phase in Gelfoam® histoculture migrated more rapidly and further than cancer cells in S/G2/M phases. Cancer cells ceased migrating when they entered S/G2/M phases and restarted migrating after cell division when the cells re-entered G0/G1. Migrating cancer cells also were resistant to cytotoxic chemotherapy, since they were preponderantly in G0/G1, where cytotoxic chemotherapy is not effective. The results of the present report suggest that novel therapy targeting G0/G1 cancer cells should be developed to prevent metastasis.

Indexed as

AdenocarcinomaAntineoplastic AgentsCell Line, TumorCell MovementCisplatinDrug Resistance, NeoplasmG1 PhaseGelatin Sponge, AbsorbableGreen Fluorescent ProteinsHumansLuminescent ProteinsMicroscopy, ConfocalNeoplasm InvasivenessRed Fluorescent ProteinResting Phase, Cell CycleStomach NeoplasmsAntineoplastic AgentsCisplatinGreen Fluorescent ProteinsLuminescent ProteinsRed Fluorescent Protein3Dcancer invasioncell cycle kineticsconfocal laser microscopyfluorescent proteinsFUCCIGelfoam histoculturereal-time imaging

Identifiers

PMID24552821
PMCPMC3984318
OpenAlexW2012091159

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.