Evidence map›Paper›PMID 35950374›Full record

ArticleCancer science2022

Induction of immunogenic cell death in murine colon cancer cells by ferrocene-containing redox phospholipid polymers.

Masahiro Kaneko, Akio Yamaguchi, Akira Ito

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 48% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
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

3 authors at 1 institution in 1 country.

Masahiro KanekoDepartment of Chemical Systems Engineering, School of Engineering, Nagoya University, Nagoya, Japan.ORCID https://orcid.org/0000-0002-8309-4086
Akio YamaguchiDepartment of Chemical Systems Engineering, School of Engineering, Nagoya University, Nagoya, Japan.
Akira ItoDepartment of Chemical Systems Engineering, School of Engineering, Nagoya University, Nagoya, Japan.ORCID https://orcid.org/0000-0001-8393-0518
Nagoya University · JP

Funding

Japan Society for the Promotion of Science 20K22465The Nitto FoundationThe Public Interest of Tatematsu
6 · The paper itself

Abstract

Immunogenic cell death (ICD), activated by damage-associated molecular patterns (DAMPs), is an apoptotic cell death process that elicits antitumor immunity. Although anticancer drugs that can induce ICD are promising for cancer treatment, the design strategy for ICD inducers remains unclear. In this study, we demonstrated the cell-penetrating redox phospholipid polymer poly(2-methacryloyloxyethyl phosphorylcholine-co-vinyl ferrocene) (pMFc) inducing ICD in murine colon cancer CT26 cells. pMFc produced oxidative stress by extracting electrons from CT26 cells and induced the release of DAMPs, such as calreticulin, adenosine triphosphate, and high-mobility group box 1. Moreover, the injection of pMFc-treated CT26 cells inhibited tumor formation in subsequently challenged CT26 cells, indicating that pMFc elicited antitumor immunity through ICD. Using in vivo therapy, intratumoral injections of pMFc induced complete tumor regression in 20% (1/5) of mice. These results suggested that the redox phospholipid polymer provides a new option for ICD-inducing anticancer polymers.

Indexed as

Antineoplastic AgentsColonic NeoplasmsAdenosine TriphosphateAnimalsCalreticulinCell Line, TumorFerrous CompoundsImmunogenic Cell DeathMetallocenesMiceOxidation-ReductionPhospholipidsPolymersAdenosine TriphosphateAntineoplastic AgentsCalreticulinferroceneFerrous CompoundsMetallocenesPhospholipidsPolymerscancer cellsimmunogenic cell deathoxidative stressphospholipid polymersredox reactions

Identifiers

PMID35950374
PMCPMC9530855
OpenAlexW4291021307

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.