Evidence map›Paper›PMID 36297426›Full record

ReviewPharmaceutics2022

Nanoparticle-Based Drug Delivery Systems Targeting Tumor Microenvironment for Cancer Immunotherapy Resistance: Current Advances and Applications.

Peijie Wu, Jun Han, Yanju Gong, Chao Liu, Han Yu, Na Xie

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.3field-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

40 citing papers in PubMed, 71 citations in OpenAlex.

  1. Review
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  5. Advancing brain immunotherapy through functional nanomaterials.Drug delivery and translational research · 2026
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  10. Inhalable nanoparticle-based drug delivery system for non-small cell lung cancer therapy: promises and challenges.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 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

6 authors at 2 institutions in 1 country.

Peijie WuSchool of Basic Medical Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu 610075, China.
Jun HanSchool of Basic Medical Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu 610075, China.
Yanju GongSchool of Basic Medical Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu 610075, China.ORCID 0000-0002-1672-5837
Chao LiuSchool of Basic Medical Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu 610075, China.
Han YuSchool of Basic Medical Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu 610075, China.
Na XieState Key Laboratory of Biotherapy and Cancer Center, West China Hospital, and West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu 610041, China.ORCID 0000-0003-3775-6277
Chengdu University of Traditional Chinese Medicine · CNSichuan University · CN

Funding

China Postdoctoral Science Foundation 2021M693784Potential Postdoctoral Program of Chengdu University of Traditional Chinese Medicine BSH2019016Potential Postdoctoral Program of Chengdu University of Traditional Chinese Medicine BSH2019019Sichuan Science and Technology Program 2022JDRC0131
6 · The paper itself

Abstract

Cancer immunotherapy has shown impressive anti-tumor activity in patients with advanced and early-stage malignant tumors, thus improving long-term survival. However, current cancer immunotherapy is limited by barriers such as low tumor specificity, poor response rate, and systemic toxicities, which result in the development of primary, adaptive, or acquired resistance. Immunotherapy resistance has complex mechanisms that depend on the interaction between tumor cells and the tumor microenvironment (TME). Therefore, targeting TME has recently received attention as a feasibility strategy for re-sensitizing resistant neoplastic niches to existing cancer immunotherapy. With the development of nanotechnology, nanoplatforms possess outstanding features, including high loading capacity, tunable porosity, and specific targeting to the desired locus. Therefore, nanoplatforms can significantly improve the effectiveness of immunotherapy while reducing its toxic and side effects on non-target cells that receive intense attention in cancer immunotherapy. This review explores the mechanisms of tumor microenvironment reprogramming in immunotherapy resistance, including TAMs, CAFs, vasculature, and hypoxia. We also examined whether the application of nano-drugs combined with current regimens is improving immunotherapy clinical outcomes in solid tumors.

Indexed as

fibroblastshypoxiaimmunotherapymacrophagesnanoparticlesoxidative stressresistancetumor microenvironmenttumor vasculature

Identifiers

PMID36297426
PMCPMC9612242
OpenAlexW4296613612

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.