Evidence map›Paper›PMID 31557421›Full record

ArticleAdvanced healthcare materials2019

Catalase-Functionalized Iron Oxide Nanoparticles Reverse Hypoxia-Induced Chemotherapeutic Resistance.

Tin-Yo Yen, Zachary R Stephen, Guanyou Lin, Qingxin Mu, Mike Jeon, Stela Untoro, Parker Welsh, Miqin Zhang

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Therapeutic Gases in Biomedicine: Updates on Nitric Oxide and Beyond.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

8 authors at 1 institution in 1 country.

Tin-Yo YenDepartment of Material Sciences and Engineering, University of Washington, Seattle, WA, 98195, USA.
Zachary R StephenDepartment of Material Sciences and Engineering, University of Washington, Seattle, WA, 98195, USA.
Guanyou LinDepartment of Material Sciences and Engineering, University of Washington, Seattle, WA, 98195, USA.
Qingxin MuDepartment of Material Sciences and Engineering, University of Washington, Seattle, WA, 98195, USA.
Mike JeonDepartment of Material Sciences and Engineering, University of Washington, Seattle, WA, 98195, USA.
Stela UntoroDepartment of Material Sciences and Engineering, University of Washington, Seattle, WA, 98195, USA.
Parker WelshDepartment of Material Sciences and Engineering, University of Washington, Seattle, WA, 98195, USA.
Miqin ZhangDepartment of Material Sciences and Engineering, University of Washington, Seattle, WA, 98195, USA.ORCID 0000-0001-8974-1494
University of Washington · US

Funding

Iron oxide nanotheranostics for breast cancerR01EB026890 · NIBIB · UNIVERSITY OF WASHINGTON · PI ZHANG, MIQIN · 2018 to 2021
$1.9M
Kyocera Professor EndowmentNIBIB NIH HHS R01 EB026890NSF NNCI-1542101
6 · The paper itself

Abstract

Intratumoral hypoxia is a major contributor to multiple drug resistance (MDR) in cancer, and can lead to poor prognosis of patients receiving chemotherapy. Development of an MDR-inhibitor that mitigates the hypoxic environment is crucial for cancer management and treatment. Reported is a biocompatible and biodegradable catalase-conjugated iron oxide nanoparticle (Cat-IONP) capable of converting reactive oxygen species to molecular oxygen to supply an oxygen source for the hypoxic tumor microenvironment. Cat-IONP demonstrates initial enzymatic activity comparable to free catalase while providing a nearly threefold increase in long-term enzymatic activity. It is demonstrated that Cat-IONP significantly reduces the in vitro expression of hypoxia-inducible factors at the transcription level in a breast cancer cell line. Co-treatment of Cat-IONP and paclitaxel (PTX) significantly increases the drug sensitivity of hypoxic-cultured cells, demonstrating greater than twofold and fivefold reduction in cell viability in comparison to cells treated only with 80 and 120 × 10

Indexed as

HypoxiaAnimalsBasic Helix-Loop-Helix ProteinsBreast NeoplasmsCatalaseCell Line, TumorCell SurvivalDrug Resistance, MultipleDrug Resistance, NeoplasmEndothelial PAS Domain-Containing Protein 1FemaleFerric CompoundsHumansHypoxia-Inducible Factor 1, alpha SubunitMetal NanoparticlesMiceBasic Helix-Loop-Helix ProteinsCatalaseEndothelial PAS Domain-Containing Protein 1Ferric Compoundsferric oxideHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitPaclitaxelbreast cancercatalasedrug deliveryhypoxia-inducible factorsiron oxide nanoparticles

Identifiers

PMID31557421
PMCPMC6919328
OpenAlexW2975470233

What OpenQuestion holds

Textmetadata
LicenceTDM
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.