Evidence map›Paper›PMID 37111794›Full record

ArticlePharmaceutics2023

Cerium End-Deposited Gold Nanorods-Based Photoimmunotherapy for Boosting Tumor Immunogenicity.

Yanlin Feng, Yumei Xu, Zhaoyang Wen, Xin Ning, Jianlin Wang, Deping Wang, Jimin Cao, Xin Zhou

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 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
0.4field-weighted citation impact, top 44% 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, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
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

8 authors at 1 institution in 1 country.

Yanlin FengKey Laboratory of Cellular Physiology, Ministry of Education, the Department of Physiology, Shanxi Medical University, Taiyuan 030001, China.ORCID 0000-0003-4857-4567
Yumei XuDepartment of Medical Imaging, Shanxi Medical University, Taiyuan 030001, China.ORCID 0000-0001-5046-5349
Zhaoyang WenKey Laboratory of Cellular Physiology, Ministry of Education, the Department of Physiology, Shanxi Medical University, Taiyuan 030001, China.
Xin NingKey Laboratory of Cellular Physiology, Ministry of Education, the Department of Physiology, Shanxi Medical University, Taiyuan 030001, China.
Jianlin WangKey Laboratory of Cellular Physiology, Ministry of Education, the Department of Physiology, Shanxi Medical University, Taiyuan 030001, China.ORCID 0000-0001-8322-9529
Deping WangKey Laboratory of Cellular Physiology, Ministry of Education, the Department of Physiology, Shanxi Medical University, Taiyuan 030001, China.
Jimin CaoKey Laboratory of Cellular Physiology, Ministry of Education, the Department of Physiology, Shanxi Medical University, Taiyuan 030001, China.
Xin ZhouKey Laboratory of Cellular Physiology, Ministry of Education, the Department of Physiology, Shanxi Medical University, Taiyuan 030001, China.
Shanxi Medical University · CN

Funding

Applied Basic Research Program of Shanxi Province 202103021224234National Natural Science Foundation of China 22007063, 81801858 and 82170523Shanxi Medical Key Science and Technology Project Plan of China 2020XM01
6 · The paper itself

Abstract

backgroundTriple-negative breast cancer (TNBC) was closely related to high metastatic risk and mortality and has not yet found a targeted receptor for targeted therapy. Cancer immunotherapy, especially photoimmunotherapy, shows promising potential in TNBC treatment because of great spatiotemporal controllability and non-trauma. However, the therapeutic effectiveness was limited by insufficient tumor antigen generation and the immunosuppressive microenvironment.

methodsWe report on the design of cerium oxide (CeO

resultsUnder near-infrared (NIR) light irradiation, CEG can efficiently generate hot electrons and avoid hot-electron recombination to release heat and form reactive oxygen species (ROS), triggering immunogenic cell death (ICD) and activating part of the immune response. Simultaneously, combining with PD-1 antibody could further enhance cytotoxic T lymphocyte infiltration.

conclusionsCompared with CBG NRs, CEG NRs showed strong photothermal and photodynamic effects to destroy tumors and activate a part of the immune response. Combining with PD-1 antibody could reverse the immunosuppressive microenvironment and thoroughly activate the immune response. This platform demonstrates the superiority of combination therapy of photoimmunotherapy and PD-1 blockade in TNBC therapy.

Indexed as

cerium end-deposited gold nanorodsPD-1 blockadephotoimmunotherapytriple-negative breast cancer

Identifiers

PMID37111794
PMCPMC10145050
OpenAlexW4366775581

What OpenQuestion holds

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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.