Evidence map›Paper›PMID 38552151›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Regulation of CTLs/Tregs via Highly Stable and Ultrasound-Responsive Cerasomal Nano-Modulators for Enhanced Colorectal Cancer Immunotherapy.

Jinxia Zhang, Lihong Sun, Ling Jiang, Xinxin Xie, Yuan Wang, Ruiqi Wu, Qingshuang Tang, Suhui Sun, Shiwei Zhu, Xiaolong Liang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

13 citing papers in PubMed, 23 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.

Jinxia ZhangInstitute of Medical Technology, Peking University Health Science Center, Beijing, 100010, P. R. China.
Lihong SunDepartment of Ultrasound, Peking University Third Hospital, Beijing, 100191, P. R. China.
Ling JiangDepartment of Ultrasound, Peking University Third Hospital, Beijing, 100191, P. R. China.
Xinxin XieDepartment of Ultrasound, Peking University Third Hospital, Beijing, 100191, P. R. China.
Yuan WangDepartment of Ultrasound, Peking University Third Hospital, Beijing, 100191, P. R. China.
Ruiqi WuDepartment of Ultrasound, Peking University Third Hospital, Beijing, 100191, P. R. China.
Qingshuang TangDepartment of Ultrasound, Peking University Third Hospital, Beijing, 100191, P. R. China.
Suhui SunDepartment of Ultrasound, Peking University Third Hospital, Beijing, 100191, P. R. China.
Shiwei ZhuDepartment of Ultrasound, Peking University Third Hospital, Beijing, 100191, P. R. China.
Xiaolong LiangInstitute of Medical Technology, Peking University Health Science Center, Beijing, 100010, P. R. China.ORCID 0000-0001-7299-3329
Ligang CuiInstitute of Medical Technology, Peking University Health Science Center, Beijing, 100010, P. R. China.
Peking University · CN

Funding

National Natural Science Foundation of China 32271443National Natural Science Foundation of China 81871363National Natural Science Foundation of China 82000509National Natural Science Foundation of China 82071941National Natural Science Foundation of China 82272019Natural Science Foundation of Beijing Municipality JQ22024Natural Science Foundation of Beijing Municipality L232087Peking University Third Hospital BYSY2015023Peking University Third Hospital BYSYZD2019018Peking University Third Hospital jyzc2018-02
6 · The paper itself

Abstract

Immunotherapy is showing good potential for colorectal cancer therapy, however, low responsive rates and severe immune-related drug side effects still hamper its therapeutic effectiveness. Herein, a highly stable cerasomal nano-modulator (DMC@P-Cs) with ultrasound (US)-controlled drug delivery capability for selective sonodynamic-immunotherapy is fabricated. DMC@P-Cs' lipid bilayer is self-assembled from cerasome-forming lipid (CFL), pyrophaeophorbid conjugated lipid (PL), and phospholipids containing unsaturated chemical bonds (DOPC), resulting in US-responsive lipid shell. Demethylcantharidin (DMC) as an immunotherapy adjuvant is loaded in the hydrophilic core of DMC@P-Cs. With US irradiation, reactive oxygen species (ROS) can be effectively generated from DMC@P-Cs, which can not only kill tumor cells for inducing immunogenic cell death (ICD), but also oxidize unsaturated phospholipids-DOPC to change the permeability of the lipid bilayers and facilitate controlled release of DMC, thus resulting in down-regulation of regulatory T cells (Tregs) and amplification of anti-tumor immune responses. After intravenous injection, DMC@P-Cs can efficiently accumulate at the tumor site, and local US treatment resulted in 94.73% tumor inhibition rate. In addition, there is no detectable systemic toxicity. Therefore, this study provides a highly stable and US-controllable smart delivery system to achieve synergistical sonodynamic-immunotherapy for enhanced colorectal cancer therapy.

Indexed as

Colorectal NeoplasmsImmunotherapyT-Lymphocytes, CytotoxicT-Lymphocytes, RegulatoryAnimalsCell Line, TumorDisease Models, AnimalDrug Delivery SystemsHumansLiposomesMiceNanoparticlesLiposomescerasomesimmunoregulationimmunotherapysonodynamic therapyultrasound‐responsive

Identifiers

PMID38552151
PMCPMC11165532
OpenAlexW4393305610

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.