Evidence map›Paper›PMID 36504435›Full record

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

Encapsulation of Platinum Prodrugs into PC7A Polymeric Nanoparticles Combined with Immune Checkpoint Inhibitors for Therapeutically Enhanced Multimodal Chemotherapy and Immunotherapy by Activation of the STING Pathway.

Xiangjie Gao, Guanxiong Lei, Bin Wang, Zhong Deng, Johannes Karges, Haihua Xiao, Donghui Tan

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 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.0field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
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  4. Chemoimmunotherapy synergism: mechanisms and clinical applications.Naunyn-Schmiedeberg's archives of pharmacology · 2025
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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

7 authors at 3 institutions in 2 countries.

Xiangjie GaoAffiliated Hospital of Xiangnan University, Chenzhou, Hunan Province, 423000, China.
Guanxiong LeiAffiliated Hospital of Xiangnan University, Chenzhou, Hunan Province, 423000, China.
Bin WangBeijing National Laboratory for Molecular Sciences, State Key Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
Zhong DengAffiliated Hospital of Xiangnan University, Chenzhou, Hunan Province, 423000, China.
Johannes KargesFaculty of Chemistry and Biochemistry, Ruhr-University Bochum, Universitätsstrasse 150, 44780, Bochum, Germany.ORCID 0000-0001-5258-0260
Haihua XiaoBeijing National Laboratory for Molecular Sciences, State Key Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.ORCID 0000-0001-8159-8187
Donghui TanAffiliated Hospital of Xiangnan University, Chenzhou, Hunan Province, 423000, China.
Chenzhou First People's Hospital · CNChinese Academy of Sciences · CNRuhr University Bochum · DE

Funding

Chenzhou Science and Technology Innovation Capability Cultivation Program lycl2021103Chenzhou Science and Technology Innovation Capability Cultivation Program lycl2021109Excellent youth fund of Hunan Provincial Department of Education 21B0748Health Commission of Hunan Province 202207012466Key project supported by Hunan Provincial Health Commission 202207012466Key project supported by the Hunan Provincial Department of Education 20A459
6 · The paper itself

Abstract

Tumor immunotherapy has emerged as one of the most promising therapeutic methods to treat cancer. Despite its clinical application, the immunosuppressive tumor microenvironment compromises the therapeutic efficiency of this technique. To overcome this limitation, many research efforts have been devoted to the development of agents that reprogram the immunosuppressive tumor microenvironment through novel mechanisms. Over the last decade, compounds that intervene through the immunogenic stimulator of interferon genes (STING) pathway have emerged with potential for clinical development. Herein, the encapsulation of chemotherapeutic platinum complexes with a polymer with a cyclic seven-membered ring (PC7A)-based polymer into pH-responsive nanoparticles for multimodal therapeutically enhanced chemotherapy and immunotherapy is presented. This study represents the first nanomaterial with a dual activation mechanism of the STING pathway through DNA fragmentation as well as PC7A binding. The combination of these nanoparticles with immune checkpoint inhibitors demonstrates to nearly fully eradicate a colorectal tumor inside the mouse model by chemotherapy and immunotherapy using the STING pathway.

Indexed as

NanoparticlesProdrugsAnimalsImmune Checkpoint InhibitorsImmunotherapyMicePlatinumPolymersImmune Checkpoint InhibitorsPlatinumPolymersProdrugsimmunotherapynanoparticleoxaliplatinpolymer with a cyclic seven-membered ring (PC7A)stimulator of interferon genes (STING)

Identifiers

PMID36504435
PMCPMC9896041
OpenAlexW4311202311

What OpenQuestion holds

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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.