Evidence map›Paper›PMID 41163954›Full record

ReviewInternational journal of nanomedicine2025

Nanotechnology-Driven Strategies in Osteosarcoma Advances in Treatment: Immunotherapy and Drug Delivery.

Wenwen Su, Yuanyuan Li, Guang Yang, Yangyang Zhao, Xinhao Zhou, Guangyao Liu, Xu Huang, Muhammad Farhan Sohail, Irshad Hussain, Qihui Liu and 1 more

Abstract readReview
In one paragraph

Review in International journal of nanomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

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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

11 authors.

Wenwen SuKey Laboratory of Pathobiology, Ministry of Education, Nanomedicine and Translational Research Center, China-Japan Union Hospital of Jilin University, Changchun, 130033, People's Republic of China.
Yuanyuan LiKey Laboratory of Pathobiology, Ministry of Education, Nanomedicine and Translational Research Center, China-Japan Union Hospital of Jilin University, Changchun, 130033, People's Republic of China.
Guang YangJilin Cancer Hospital, Changchun, Jilin Province, 130012, People's Republic of China.
Yangyang ZhaoKey Laboratory of Pathobiology, Ministry of Education, Nanomedicine and Translational Research Center, China-Japan Union Hospital of Jilin University, Changchun, 130033, People's Republic of China.
Xinhao ZhouKey Laboratory of Pathobiology, Ministry of Education, Nanomedicine and Translational Research Center, China-Japan Union Hospital of Jilin University, Changchun, 130033, People's Republic of China.
Guangyao LiuDepartment of Orthopedics, China-Japan Union Hospital of Jilin University, Changchun, 130033, People's Republic of China.
Xu HuangDepartment of Radiology, The First Hospital of Jilin University, Changchun, 130021, People's Republic of China.
Muhammad Farhan SohailRiphah Institute of Pharmaceutical Sciences (RIPS), Riphah International University, Lahore Campus, Lahore, 54000, Pakistan.
Irshad HussainDepartment of Chemistry and Chemical Engineering, Syed Babar Ali School of Science and Engineering, Lahore University of Management Sciences, Lahore, Punjab, 54792, Pakistan.ORCID 0000-0001-5498-1236
Qihui LiuKey Laboratory of Pathobiology, Ministry of Education, Nanomedicine and Translational Research Center, China-Japan Union Hospital of Jilin University, Changchun, 130033, People's Republic of China.ORCID 0000-0002-8985-1906
Fangfang ChenKey Laboratory of Pathobiology, Ministry of Education, Nanomedicine and Translational Research Center, China-Japan Union Hospital of Jilin University, Changchun, 130033, People's Republic of China.ORCID 0000-0002-3284-3331

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma (OS), the most prevalent primary malignant bone tumor, exhibits highly aggressive and metastatic potential, accounting approximately 56% of all primary malignant bone malignancies. While neoadjuvant chemotherapy with surgery remains standard, challenges persist: suboptimal margins, non-specific drug biodistribution, and systemic toxicity. Nanomaterial engineering offers transformative multifunctional platforms, integrating biomimetic targeting, stimuli-responsive release, and theranostics to enhance tumor penetration and reduce off-target effects. Immunotherapy combats OS by activating antitumor immunity, reprogramming the immunosuppressive tumor microenvironment (TME), and synergizing with checkpoint inhibitors/cell therapies. Ligand-functionalized nanocarriers significantly improve chemotherapeutic bioavailability and targeting. This review systematically explores the dual role of nanoplatforms in osteosarcoma therapeutics: (1) immunotherapy via TME reprogramming and (2) precision oncology through advanced drug delivery paradigms, providing critical insights into their translational potential for overcoming current therapeutic bottlenecks and ultimately improving clinical outcomes for OS patients.

Indexed as

Bone NeoplasmsDrug Delivery SystemsImmunotherapyOsteosarcomaAnimalsAntineoplastic AgentsHumansNanomedicineNanoparticlesNanotechnologyTheranostic NanomedicineTumor MicroenvironmentAntineoplastic Agentsdrug deliveryimmune regulationnanomaterialsosteosarcomatumor microenvironment

Identifiers

PMID41163954
PMCPMC12560659

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.