Evidence map›Paper›PMID 40699365›Full record

ArticleEuropean journal of orthopaedic surgery & traumatology : orthopedie traumatologie2025

Cluster of differentiation 133 (CD133) and C-X-C chemokine receptor 4 (CXCR4) associated with the incidence of metastasis in osteosarcoma patients.

Nyoman Gede Bimantara, Achmad Fauzi Kamal, Po-Kuei Wu, I Gede Eka Wiratnaya, Herqutanto Herqutanto, Aryadi Kurniawan, Yogi Prabowo, Istan Irmansyah Irsan, Naseh Sajadi Budi Irawan, Nuryati Chairani Siregar

Abstract readMulticenter Study
In one paragraph

Article in European journal of orthopaedic surgery & traumatology : orthopedie traumatologie, 2025. 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

10 authors.

Nyoman Gede BimantaraDepartment of Orthopaedics and Traumatology, Faculty of Medicine, Universitas Indonesia - Cipto Mangunkusumo General Hospital, Jakarta, Indonesia.
Achmad Fauzi KamalDepartment of Orthopaedics and Traumatology, Faculty of Medicine, Universitas Indonesia - Cipto Mangunkusumo General Hospital, Jakarta, Indonesia. fauzikamal@yahoo.com.
Po-Kuei WuDepartment of Orthopaedics and Traumatology, Taipei Veterans General Hospital, Taipei, Taiwan.
I Gede Eka WiratnayaDepartment of Orthopaedics and Traumatology, Faculty of Medicine, Universitas Udayana, Denpasar, Indonesia.
Herqutanto HerqutantoDepartment of Orthopaedics and Traumatology, Faculty of Medicine, Universitas Indonesia - Cipto Mangunkusumo General Hospital, Jakarta, Indonesia.
Aryadi KurniawanDepartment of Orthopaedics and Traumatology, Faculty of Medicine, Universitas Indonesia - Cipto Mangunkusumo General Hospital, Jakarta, Indonesia.
Yogi PrabowoDepartment of Orthopaedics and Traumatology, Faculty of Medicine, Universitas Indonesia - Cipto Mangunkusumo General Hospital, Jakarta, Indonesia.
Istan Irmansyah IrsanDepartment of Orthopaedics and Traumatology, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia.
Naseh Sajadi Budi IrawanDepartment of Orthopaedics and Traumatology, Faculty of Medicine, Universitas Padjajaran, Bandung, Indonesia.
Nuryati Chairani SiregarDepartment of Orthopaedics and Traumatology, Faculty of Medicine, Universitas Indonesia - Cipto Mangunkusumo General Hospital, Jakarta, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteosarcoma has a global incidence of 3.4 cases per million annually, with 10-20% of patients presenting with metastasis at diagnosis. Its high metastatic potential is attributed to a highly proliferative cell population and cancer stem cells that drive tumorigenesis and metastasis. This study examines the relationship between CD133 and CXCR4 expression and metastasis in osteosarcoma.

methodsUsing a cross-sectional approach, blood serum from osteosarcoma patients diagnosed at two centers was analyzed for CD133 and CXCR4 levels via Reed Biotech ELISA KIT. Absorbance quantified marker levels, and metastasis data were obtained from medical records. A chi-square test assessed the relationship between marker levels and metastasis, with significance set at p < 0.05.

resultsAmong 40 patients (80% < 40 years), mean CD133 was 0.23 ± 0.02 pg/ml and mean CXCR4 was 6015.82 ± 2345.55 pg/ml. CD133 and CXCR4 levels were significantly associated with metastasis (p = 0.009 and p < 0.001, respectively).

conclusionThese findings suggest that higher expression of CD133 and CXCR4 correlates with increased metastasis in osteosarcoma, underscoring their potential roles in predicting metastatic behavior and aiding in targeted therapeutic strategies.

Indexed as

AC133 AntigenBone NeoplasmsOsteosarcomaReceptors, CXCR4AdolescentAdultBiomarkers, TumorChildCross-Sectional StudiesFemaleHumansIncidenceMaleMiddle AgedNeoplasm MetastasisYoung AdultAC133 AntigenBiomarkers, TumorCXCR4 protein, humanPROM1 protein, humanReceptors, CXCR4CD133CXCR4MetastasisOsteosarcoma

Identifiers

PMID40699365
PMCPMC12287143

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.