Evidence map›Paper›PMID 37957541›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2023

Implanted, Wireless, Self-Powered Photodynamic Therapeutic Tablet Synergizes with Ferroptosis Inducer for Effective Cancer Treatment.

Pingjin Zou, Rui Lin, Zengyi Fang, Junyang Chen, Hongye Guan, Jie Yin, Zhiheng Chang, Lili Xing, Jinyi Lang, Xinyu Xue and 1 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Pingjin ZouSchool of Medicine, University of Electronic Science and Technology of China, Chengdu, 610054, China.ORCID 0000-0003-0480-5263
Rui LinSchool of Physics, University of Electronic Science and Technology of China, Chengdu, 611731, China.
Zengyi FangSchool of Medicine, University of Electronic Science and Technology of China, Chengdu, 610054, China.
Junyang ChenDepartment of Radiation Oncology, Radiation Oncology Key Laboratory of Sichuan Province, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Center, Sichuan Cancer Hospital & Institute, Affiliated Cancer Hospital of University of Electronic Science and Technology of China, Chengdu, 610042, China.
Hongye GuanSchool of Physics, University of Electronic Science and Technology of China, Chengdu, 611731, China.
Jie YinSchool of Medicine, University of Electronic Science and Technology of China, Chengdu, 610054, China.
Zhiheng ChangSchool of Computer Science and Engineering, University of Electronic Science and Technology of China, Chengdu, 611731, China.
Lili XingSchool of Physics, University of Electronic Science and Technology of China, Chengdu, 611731, China.
Jinyi LangSchool of Medicine, University of Electronic Science and Technology of China, Chengdu, 610054, China.
Xinyu XueSchool of Physics, University of Electronic Science and Technology of China, Chengdu, 611731, China.
Meihua ChenDepartment of Radiation Oncology, Radiation Oncology Key Laboratory of Sichuan Province, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Center, Sichuan Cancer Hospital & Institute, Affiliated Cancer Hospital of University of Electronic Science and Technology of China, Chengdu, 610042, China.ORCID 0000-0003-2813-7423
University of Electronic Science and Technology of China · CN

Funding

Beijing Xisike Clinical Oncology Research Foundation Y-XD202001-0024National Natural Science Foundation of China 81703070Sichuan Science and Technology Program 2020YJ0446Sichuan Science and Technology Program 2023NSFSC0708
6 · The paper itself

Abstract

The effective and targeted treatment of resistant cancer cells presents a significant challenge. Targeting cell ferroptosis has shown remarkable efficacy against apoptosis-resistant tumors due to their elevated iron metabolism and oxidative stress levels. However, various obstacles have limited its effectiveness. To overcome these challenges and enhance ferroptosis in cancer cells, we have developed a self-powered photodynamic therapeutic tablet that integrates a ferroptosis inducer (FIN), imidazole ketone erastin (IKE). FINs augment the sensitivity of photodynamic therapy (PDT) by increasing oxidative stress and lipid peroxidation. Furthermore, they utilize the Fenton reaction to supplement oxygen, generating a greater amount of reactive oxygen species (ROS) during PDT. Additionally, PDT facilitates the release of iron ions from the labile iron pool (LIP), accelerating lipid peroxidation and inducing ferroptosis. In vitro and in vivo experiments have demonstrated a more than 85% tumor inhibition rate. This synergistic treatment approach not only addresses the limitations of inadequate penetration and tumor hypoxia associated with PDT but also reduces the required medication dosage. Its high efficiency and specificity towards targeted cells minimize adverse effects, presenting a novel approach to combat clinical resistance in cancer treatment.

Indexed as

FerroptosisNeoplasmsHumansIronProstheses and ImplantsTreatment OutcomeIronferroptosis inducersimplanted tabletphotodynamic therapeutic tabletself-powered unitsynergistic therapywireless power unit

Identifiers

PMID37957541
PMCPMC10754143
OpenAlexW4388671251

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.