Evidence map›Paper›PMID 38126905›Full record

ReviewSmall (Weinheim an der Bergstrasse, Germany)2024

Nanotechnology Applications in Breast Cancer Immunotherapy.

Ruijie Wang, Pramod Kumar, Moataz Reda, Alyssa G Wallstrum, Noah A Crumrine, Worapol Ngamcherdtrakul, Wassana Yantasee

Open access · greenAbstract readReview
In one paragraph

Review in Small (Weinheim an der Bergstrasse, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 22 citations in OpenAlex.

  1. Sulfur Vacancy-Enriched CuAngewandte Chemie (International ed. in English) · 2026
    Article
  2. Selenium-Containing Compounds in Breast Cancer Therapy.Biological trace element research · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Emerging Nanozyme Strategies for Precision Breast Cancer Treatment.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
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 2 institutions in 1 country.

Ruijie WangDepartment of Biomedical Engineering, Oregon Health & Science University, 3303 S Bond Ave, Portland, OR, 97239, USA.
Pramod KumarDepartment of Biomedical Engineering, Oregon Health & Science University, 3303 S Bond Ave, Portland, OR, 97239, USA.
Moataz RedaPDX Pharmaceuticals, 3303 S Bond Ave, CH13B, Portland, OR, 97239, USA.
Alyssa G WallstrumPDX Pharmaceuticals, 3303 S Bond Ave, CH13B, Portland, OR, 97239, USA.
Noah A CrumrinePDX Pharmaceuticals, 3303 S Bond Ave, CH13B, Portland, OR, 97239, USA.
Worapol NgamcherdtrakulPDX Pharmaceuticals, 3303 S Bond Ave, CH13B, Portland, OR, 97239, USA.ORCID 0000-0003-4187-7709
Wassana YantaseeDepartment of Biomedical Engineering, Oregon Health & Science University, 3303 S Bond Ave, Portland, OR, 97239, USA.ORCID 0000-0002-0989-363X
PDX Pharmaceuticals (United States) · USOregon Health & Science University · US

Funding

PLK1 and EGFR targeted nanoconstruct as a monotherapy and a radiation sensitizer for lung cancerR44CA285233 · NCI · PDX PHARMACEUTICALS, INC. · PI NGAMCHERDTRAKUL, WORAPOL, YANTASEE, WASSANA · 2023 to 2025
$2.6M
Novel Nano-immunotherapy for Treatment of Non-small Cell Lung CancerR44CA265751 · NCI · PDX PHARMACEUTICALS, INC. · PI NGAMCHERDTRAKUL, WORAPOL, YANTASEE, WASSANA · 2021 to 2024
$2.2M
In Situ Tumor Vaccination with a Nano-oligo Therapeutic to Induce Whole-body Antitumor Immune ResponseR44CA265752 · NCI · PDX PHARMACEUTICALS, INC. · PI NGAMCHERDTRAKUL, WORAPOL, YANTASEE, WASSANA · 2021 to 2022
$2.0M
Kuni FoundationNCI NIH HHS R44 CA265751NCI NIH HHS R44CA265751NCI NIH HHS R44 CA265752NCI NIH HHS R44CA265752NCI NIH HHS R44 CA285233NCI NIH HHS R44CA285233
6 · The paper itself

Abstract

Next-generation cancer treatments are expected not only to target cancer cells but also to simultaneously train immune cells to combat cancer while modulating the immune-suppressive environment of tumors and hosts to ensure a robust and lasting response. Achieving this requires carriers that can codeliver multiple therapeutics to the right cancer and/or immune cells while ensuring patient safety. Nanotechnology holds great potential for addressing these challenges. This article highlights the recent advances in nanoimmunotherapeutic development, with a focus on breast cancer. While immune checkpoint inhibitors (ICIs) have achieved remarkable success and lead to cures in some cancers, their response rate in breast cancer is low. The poor response rate in solid tumors is often associated with the low infiltration of anti-cancer T cells and an immunosuppressive tumor microenvironment (TME). To enhance anti-cancer T-cell responses, nanoparticles are employed to deliver ICIs, bispecific antibodies, cytokines, and agents that induce immunogenic cancer cell death (ICD). Additionally, nanoparticles are used to manipulate various components of the TME, such as immunosuppressive myeloid cells, macrophages, dendritic cells, and fibroblasts to improve T-cell activities. Finally, this article discusses the outlook, challenges, and future directions of nanoimmunotherapeutics.

Indexed as

Breast NeoplasmsImmunotherapyNanotechnologyAnimalsFemaleHumansNanoparticlesTumor Microenvironmentbreast cancerimmunosuppressionimmunotherapynanoparticletumor microenvironment

Identifiers

PMID38126905
PMCPMC11493329
OpenAlexW4390049658

What OpenQuestion holds

Textmetadata
LicenceTDM
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.