Evidence map›Paper›PMID 36655546›Full record

ArticleThoracic cancer2023

Development of a new minimally invasive phototherapy for lung cancer using antibody-toxin conjugate.

Takumi Sonokawa, Naoko Obi, Jitsuo Usuda, Yukio Sudo, Takao Hamakubo

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
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  4. Review
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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

5 authors at 2 institutions in 1 country.

Takumi SonokawaDepartment of Thoracic Surgery, Nippon Medical School, Tokyo, Japan.ORCID 0000-0002-6567-9443
Naoko ObiResearch & Development Division, PhotoQ3 Inc., Tokyo, Japan.
Jitsuo UsudaDepartment of Thoracic Surgery, Nippon Medical School, Tokyo, Japan.
Yukio SudoResearch & Development Division, PhotoQ3 Inc., Tokyo, Japan.
Takao HamakuboResearch & Development Division, PhotoQ3 Inc., Tokyo, Japan.
Ajinomoto (Japan) · JPNippon Medical School Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPhotodynamic therapy (PDT) is a cancer-targeted treatment that uses a photosensitizer (PS) and laser irradiation. The effectiveness of current PDT using red light for advanced cancers is limited, because red light can only reach depths within a few millimeters. To enhance the antitumor effect for lung cancers, we developed a new phototherapy, intelligent targeted antibody phototherapy (iTAP). This treatment uses a combination of immunotoxin and a PS, mono-L-aspartyl chlorin e6 (NPe6).

methodsWe examined whether cetuximab encapsulated in endosomes was released into the cytosol by PS in PDT under light irradiation. A431 cells were treated with fluorescein isothiocyanate-labeled cetuximab, NPe6, and light irradiation and were observed with fluorescence microscopy. We analyzed the cytotoxicity of saporin-conjugated cetuximab (IT-cetuximab) in A431, A549, and MCF7 cells and the antitumor effect in model A549-bearing mice in vivo using the iTAP method.

resultsFluorescent microscopy analysis showed that the photodynamic effect of NPe6 (20 μM) and light irradiation (37.6 J/cm

conclusionsOur study is the first report of the iTAP method using NPe6 for lung cancer cells. The iTAP method may become a new, minimally invasive treatment superior to current PDT methods.

Indexed as

ImmunotoxinsLung NeoplasmsPhotochemotherapyAnimalsCetuximabHumansMicePhotosensitizing AgentsPhototherapyCetuximabImmunotoxinsPhotosensitizing Agentsdrug delivery systemendosomal escapeimmunotoxinmono-l-aspartyl chlorin e6 (NPe6)photodynamic therapy

Identifiers

PMID36655546
PMCPMC9981311
OpenAlexW4317480439

What OpenQuestion holds

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LicenceCC BY
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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.