Evidence map›Paper›PMID 34948143›Full record

ArticleInternational journal of molecular sciences2021

Synergistic Effect of Repolarization of M2 to M1 Macrophages Induced by Iron Oxide Nanoparticles Combined with Lactate Oxidase.

Zi-Xian Liao, Da-Liang Ou, Ming-Jung Hsieh, Chia-Chen Hsieh

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

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  12. [Research progress on the effect of iron oxide nanoparticles in macrophage polarization].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 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

4 authors at 2 institutions in 1 country.

Zi-Xian LiaoInstitute of Medical Science and Technology, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.ORCID 0000-0002-3051-0728
Da-Liang OuGraduate Institute of Oncology, College of Medicine, National Taiwan University, Taipei 10051, Taiwan.ORCID 0000-0002-8368-1141
Ming-Jung HsiehInstitute of Medical Science and Technology, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.
Chia-Chen HsiehInstitute of Medical Science and Technology, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.ORCID 0000-0001-6521-7620
National Sun Yat-sen University · TWNational Taiwan University · TW

Funding

Taiwan Ministry of Science and Technology MOST 108-2628-B-110-001Taiwan Ministry of Science and Technology MOST 108-2628-E-110-003-MY3Taiwan Ministry of Science and Technology MOST 109-2628-B-110-003Taiwan Ministry of Science and Technology MOST 110-2628-B-110-003
6 · The paper itself

Abstract

Metabolic reprogramming of tumors with the accompanying reprogramming of glucose metabolism and production of lactate accumulation is required for the subsequent development of tumors. Recent evidence has indicated that tumor-secreted lactate can promote an oncolytic immune microenvironment within the tumor. Furthermore, tumor-secreted lactate directly induces polarization of tumor-supportive M2 macrophages. However, oxidized tumor-secreted lactate in the tumor microenvironment can be exploited. Iron oxide nanoparticles have shown promising anticancer potential by activating tumor-suppressing macrophages. Furthermore, lactate oxidase (LOX) generally oxidizes tumor-secreted lactate and subsequently converts to pyruvate. Particularly, the ratio of M2 macrophages to M1 macrophages corresponds with tumor growth. In this study, we present iron oxide nanoparticles with carboxylic acid combined with LOX that enhance antitumor efficacy as a synergistic effect on the repolarization of tumor-supportive M2 macrophages to tumor-suppressive M1 macrophages in a tumor microenvironment. After M2 macrophages treated with iron oxide nanoparticles were combined with LOX, the ratio of M1 macrophages was significantly greater than iron oxide nanoparticles alone or with LOX alone. It is concluded that the inhibition of cancer cell proliferation by ratio of M1 macrophages was observed. This study suggests that the iron oxide nanoparticles combined with LOX could be potentially used for potentiating immune checkpoint inhibitor therapies for cancer treatment.

Indexed as

Magnetic Iron Oxide NanoparticlesAnimalsHumansMacrophagesMiceMixed Function OxygenasesNeoplasmsRAW 264.7 CellsTumor Microenvironmentlactate 2-monooxygenaseMixed Function Oxygenasesiron oxide nanoparticleslactatelactate oxidasemacrophagesynergistic effect

Identifiers

PMID34948143
PMCPMC8705044
OpenAlexW4200282754

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.