Evidence map›Paper›PMID 30705336›Full record

ArticleScientific reports2019

Anticancer polymers designed for killing dormant prostate cancer cells.

Haruko Takahashi, Kenji Yumoto, Kazuma Yasuhara, Enrico T Nadres, Yutaka Kikuchi, Laura Buttitta, Russell S Taichman, Kenichi Kuroda

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 55 citations in OpenAlex.

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  14. The Influence of Cell Cycle Regulation on Chemotherapy.International journal of molecular sciences · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Haruko TakahashiDepartment of Biologic and Materials Sciences, School of Dentistry, University of Michigan, Ann Arbor, MI, 48109, USA.
Kenji YumotoDepartment of Periodontics & Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, MI, 48109, USA.
Kazuma YasuharaDivision of Materials Science, Graduate School of Science and Technology, Nara Institute of Science and Technology, Ikoma, Nara, 630-0192, Japan.
Enrico T NadresDepartment of Biologic and Materials Sciences, School of Dentistry, University of Michigan, Ann Arbor, MI, 48109, USA.
Yutaka KikuchiDepartment of Biological Science, Graduate School of Science, Hiroshima University, 1-3-1 Kagamiyama, Higashi-hiroshima, Hiroshima, 739-8526, Japan.
Laura ButtittaMolecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI, 48109, USA.
Russell S TaichmanDepartment of Periodontics & Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, MI, 48109, USA. kkuroda@umich.edu.ORCID 0000-0002-7890-0020
Kenichi KurodaDepartment of Biologic and Materials Sciences, School of Dentistry, University of Michigan, Ann Arbor, MI, 48109, USA.
University of Michigan · USHiroshima University · JPNara Institute of Science and Technology · JP

Funding

Tumor microvesicle-mediated modulation of the bone microenvironmentP01CA093900 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KELLER, EVAN T · 2004 to 2024
$29.6M
Mechanisms That Regulate Dormancy of Disseminated Tumor Cells in the Bone MarrowU54CA163124 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHIOZAWA, YUSUKE · 2011 to 2015
$3.0M
NCI NIH HHS P01 CA093900NCI NIH HHS U54 CA163124
6 · The paper itself

Abstract

The discovery of anticancer therapeutics effective in eliminating dormant cells is a significant challenge in cancer biology. Here, we describe new synthetic polymer-based anticancer agents that mimic the mode of action of anticancer peptides. These anticancer polymers developed here are designed to capture the cationic, amphiphilic traits of anticancer peptides. The anticancer polymers are designed to target anionic lipids exposed on the cancer cell surfaces and act by disrupting the cancer cell membranes. Because the polymer mechanism is not dependent on cell proliferation, we hypothesized that the polymers were active against dormant cancer cells. The polymers exhibited cytotoxicity to proliferating prostate cancer. Importantly, the polymer killed dormant prostate cancer cells that were resistant to docetaxel. This study demonstrates a new approach to discover novel anticancer therapeutics.

Indexed as

Antineoplastic AgentsBiomimeticsCell Line, TumorCell ProliferationHumansMaleMolecular StructurePolymersProstatic NeoplasmsAntineoplastic AgentsPolymers

Identifiers

PMID30705336
PMCPMC6355926
OpenAlexW2912536499

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.