Evidence map›Paper›PMID 42326738›Full record

ReviewBone reports2026

Genomic landscape and tumor immune microenvironment of osteosarcoma: Bridging mechanistic insights to precision therapeutics.

Chenchen Yang, Yiyang Yu, Yaqi Wang, Zhenyu Cai, Yuwei Zhao, Hengyue Ma, Jie Xu, Huaiqiu Zhu, Tingting Ren, Xiaodong Tang and 1 more

Abstract readReview
In one paragraph

Review in Bone reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Chenchen YangMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, PR China.
Yiyang YuMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, PR China.
Yaqi WangCollege of Future Technology, Peking University, Beijing, PR China.
Zhenyu CaiMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, PR China.
Yuwei ZhaoMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, PR China.
Hengyue MaMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, PR China.
Jie XuMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, PR China.
Huaiqiu ZhuCollege of Future Technology, Peking University, Beijing, PR China.
Tingting RenMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, PR China.
Xiaodong TangMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, PR China.
Lu XieMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Osteosarcoma (OTS) is a highly aggressive primary bone malignancy characterized by profound genomic instability and a complex, immunosuppressive tumor immune microenvironment (TIME). Despite the established standard of neoadjuvant chemotherapy and surgical resection, the 5-year overall survival rates for metastatic or relapsed disease have remained stagnant at approximately 40% for decades. The high degree of heterogeneity and the "immune cold" nature of OTS pose significant challenges to the efficacy of conventional and emerging therapies. This review aims to summarize recent advances in the genomic and immunological landscape of OTS to inform personalized precision medicine. Main body: Genomic profiling reveals that OTS is driven by large-scale structural variations rather than single oncogenic drivers, with chromothripsis occurring in over 70% of cases. Frequent alterations in tumor suppressor genes, such as Conclusion: The transition from universal treatment to precision therapy in OTS requires a multi-omics approach for patient stratification. Future strategies must focus on overcoming the physical and immunological barriers of the TIME, reprogramming immunosuppressive cells, and exploiting novel targets like B7-H3 and MTAP deletion to improve outcomes for patients with advanced disease.

Indexed as

GenomicsImmune microenvironmentImmunotherapyOsteosarcomaPrecision therapy

Identifiers

PMID42326738
PMCPMC13279201

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LicenceCC BY-NC-ND
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Registered trials

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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.