Evidence mapPaperPMID 40152485Full record

ArticleCancer medicine2025

Expression of Cancer-Testis Antigens MAGE-A1, MAGE-A4, NY-ESO-1 and PRAME in Bone and Soft Tissue Sarcomas: The Experience From a Single Center in China.

Anni Chen, Yuling Qiu, Ying-Tzu Yen, Chun Wang, Xiaolu Wang, Chunhua Li, Zijian Wei, Lin Li, Lixia Yu, Fangcen Liu and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Cancer medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Anni ChenNanjing University of Chinese Medicine, Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Yuling QiuThe Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University and Clinical Cancer Institute of Nanjing University, Nanjing, China.
Ying-Tzu YenThe Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University and Clinical Cancer Institute of Nanjing University, Nanjing, China.
Chun WangThe Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University and Clinical Cancer Institute of Nanjing University, Nanjing, China.
Xiaolu WangThe Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University and Clinical Cancer Institute of Nanjing University, Nanjing, China.
Chunhua LiNanjing University of Chinese Medicine, Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Zijian WeiNanjing University of Chinese Medicine, Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Lin LiThe Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University and Clinical Cancer Institute of Nanjing University, Nanjing, China.
Lixia YuThe Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University and Clinical Cancer Institute of Nanjing University, Nanjing, China.
Fangcen LiuNanjing University of Chinese Medicine, Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Rutian LiNanjing University of Chinese Medicine, Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.ORCID https://orcid.org/0000-0003-4800-6156

Funding

Fundings for Clinical Trials from the Affiliated Drum Tower Hospital, Medical School of Nanjing University 2022-LCYJ-PY-21National Natural Science Foundation of China 82272852Project supported by the Young Scientists Fund of the National Natural Science Foundation of China 82203178Science Fund for Distinguished Young Scholars of Jiangsu Province BK20240017The Youth Fund Project of Natural Science Foundation of Jiangsu Province Basic Research Program BK20220191Youth project of Nanjing Medical Science and Technology Development Fund YKK22086
6 · The paper itself

Abstract

objectiveSarcomas are a heterogeneous group of malignancies, low disease-control levels and the limited durability of responses have prompted the exploration of various novel immunotherapeutic approaches. To preliminarily explore the feasibility of cancer vaccines based on cancer testis antigen in the immunotherapy of sarcomas, we investigate the expression of Cancer/Testis Antigens (CTA) MAGE-A4, PRAME, MAGE-A1, KK-LC-1, and NY-ESO-1 in bone and soft tissue sarcomas, with the aim of assessing their potential for use in sarcoma immunotherapy and determining their expression levels in different subtypes. METHODS AND

resultsWe employed immunohistochemistry and multiplex immunostaining microarrays (MI chips) to assess the expression of MAGE-A4, PRAME, MAGE-A1, KK-LC-1, and NY-ESO-1 in 21 cases of undifferentiated pleomorphic sarcoma (UPS), 26 cases of smooth muscle sarcoma, 28 cases of liposarcoma, 40 cases of osteosarcoma (OS), and 13 cases of chondrosarcoma. MAGE-A1 showed the highest expression in osteosarcoma (32.50%), while it was lower in liposarcoma and undifferentiated pleomorphic sarcoma (10.71% and 10.00%) and undetectable in chondrosarcoma. MAGE-A4 expression was elevated in osteosarcoma and undifferentiated pleomorphic sarcoma (40.00% and 33.00%), but lower in liposarcoma and smooth muscle sarcoma (17.00% and 33.00%). NY-ESO-1 expression was relatively low across all sarcoma subtypes. PRAME expression was highest in undifferentiated pleomorphic sarcoma (47.62%) and low in chondrosarcoma (7.69%). None of the sarcomas expressed KK-LC-1. Additionally, while there was no statistically significant correlation between CTA expression and patient age or gender, some differences related to age and gender were observed.

conclusionsCTA expression in bone and soft tissue sarcomas was correlated with both CTA type and sarcoma subtype, showing relatively high levels of expression in undifferentiated pleomorphic sarcoma (UPS) and osteosarcoma (OS). The poly-expression of MAGE-A4, PRAME, and MAGE-A1 across all subtypes suggests that these antigens may serve as potential targets for sarcoma-specific immunotherapy.

Indexed as

Antigens, NeoplasmBone NeoplasmsMelanoma-Specific AntigensMembrane ProteinsNeoplasm ProteinsSarcomaSoft Tissue NeoplasmsAdolescentAdultAgedBiomarkers, TumorChildChinaFemaleHumansImmunohistochemistryAntigens, NeoplasmBiomarkers, TumorCTAG1B protein, humanMAGE-A1 protein (278-286), humanMAGEA4 protein, humanMelanoma-Specific AntigensMembrane ProteinsNeoplasm ProteinsPeptide FragmentsPRAME protein, humancancer testis antigenimmunotherapyMAGE‐A4NY‐ESO‐1sarcoma

Identifiers

PMID40152485
PMCPMC11951172

What Socratic holds

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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 Socratic graph.