Evidence map›Paper›PMID 38286035›Full record

ArticleACS nano2024

Immunogenic Bifunctional Nanoparticle Suppresses Programmed Cell Death-Ligand 1 in Cancer and Dendritic Cells to Enhance Adaptive Immunity and Chemo-Immunotherapy.

Jing Liu, Xiaomin Jiang, Youyou Li, Kaiting Yang, Ralph R Weichselbaum, Wenbin Lin

Open access · greenAbstract read
In one paragraph

Article in ACS nano, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Unravelling the pathogenesis and therapeutic approaches of pancreatic ductal adenocarcinoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

6 authors at 1 institution in 1 country.

Jing LiuDepartment of Chemistry, University of Chicago, 929 East 57th Street, Chicago, Illinois 60637, United States.ORCID 0009-0007-4907-0228
Xiaomin JiangDepartment of Chemistry, University of Chicago, 929 East 57th Street, Chicago, Illinois 60637, United States.ORCID 0000-0001-8304-4938
Youyou LiDepartment of Chemistry, University of Chicago, 929 East 57th Street, Chicago, Illinois 60637, United States.
Kaiting YangDepartment of Radiation and Cellular Oncology and Ludwig Center for Metastasis Research, University of Chicago, 5758 South Maryland Avenue, Chicago, Illinois 60637, United States.
Ralph R WeichselbaumDepartment of Radiation and Cellular Oncology and Ludwig Center for Metastasis Research, University of Chicago, 5758 South Maryland Avenue, Chicago, Illinois 60637, United States.
Wenbin LinDepartment of Chemistry, University of Chicago, 929 East 57th Street, Chicago, Illinois 60637, United States.ORCID 0000-0001-7035-7759
University of Chicago · US

Funding

Radiation Effect on Immune Cells and the MicrobiomeU54CA274291 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI Silvia C. Formenti · 2022 to 2026
$9.1M
Tumor-Targeted Multimodality Nanoscale Coordination Polymers for Chemo-Immunotherapy of Metastatic Colorectal CancerR01CA279802 · NCI · UNIVERSITY OF CHICAGO · PI RALPH R WEICHSELBAUM · 2023 to 2026
$1.8M
Nanoscale Coordination Polymers of Cyclic-di-nucleotides and Peptide Antigens for Effective Therapy of Metastatic Colorectal CancerR01CA276307 · NCI · UNIVERSITY OF CHICAGO · PI RALPH R WEICHSELBAUM · 2023 to 2026
$1.8M
NCI NIH HHS R01 CA276307NCI NIH HHS R01 CA279802NCI NIH HHS U54 CA274291
6 · The paper itself

Abstract

Blockade of programmed cell death-1/programmed cell death-ligand 1 (PD-L1) immune checkpoints with monoclonal antibodies has shown great promise for cancer treatment, but these antibodies can cause immune-related adverse events in normal organs. Here we report a dual-cell targeted chemo-immunotherapeutic nanoscale coordination polymer (NCP), OxPt/BP, comprising oxaliplatin (OxPt) and 2-bromopalmitic acid (BP), for effective downregulation of PD-L1 expression in both cancer cells and dendritic cells (DCs) by inhibiting palmitoyl acyltransferase DHHC3. OxPt/BP efficiently promotes DC maturation by increasing intracellular oxidative stress and enhancing OxPt-induced immunostimulatory immunogenic cancer cell death. Systemic administration of OxPt/BP reduces the growth of subcutaneous and orthotopic colorectal carcinoma by facilitating the infiltration and activation of cytotoxic T lymphocytes together with reducing the population of immunosuppressive regulatory T cells. As a result, OxPt/BP significantly extends mouse survival without causing side effects. This work highlights the potential of NCPs in simultaneously reprogramming cancer cells and DCs for potent cancer treatment.

Indexed as

B7-H1 AntigenNeoplasmsAdaptive ImmunityAnimalsApoptosisCell Line, TumorDendritic CellsImmunotherapyLigandsMiceB7-H1 AntigenLigands2-bromopalmitateadaptive immunitychemo-immunotherapydendritic cell regulationnanoscale coordination polymerprogrammed cell death-ligand 1

Identifiers

PMID38286035
PMCPMC11776391
OpenAlexW4391303982

What OpenQuestion holds

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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.