Evidence map›Paper›PMID 37681913›Full record

ArticleCells2023

Comparative Shotgun Proteomics Reveals the Characteristic Protein Signature of Osteosarcoma Subtypes.

Maram Alaa, Nouran Al-Shehaby, Ali Mostafa Anwar, Nesma Farid, Mustafa Shaban Shawky, Manal Zamzam, Iman Zaky, Ahmed Elghounimy, Shahenda El-Naggar, Sameh Magdeldin

Abstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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.

Maram AlaaImmunology and Microbiology Research Program, Basic Research Unit, Research Department, Children's Cancer Hospital Egypt 57357, Cairo 11441, Egypt.
Nouran Al-ShehabyTumor Biology Research Program, Basic Research Unit, Research Department, Children's Cancer Hospital Egypt 57357, Cairo 11441, Egypt.
Ali Mostafa AnwarProteomics and Metabolomics Research Program, Basic Research Unit, Research Department, Children's Cancer Hospital Egypt 57357, Cairo 11441, Egypt.
Nesma FaridClinical Research Unit, Research Department, Children's Cancer Hospital Egypt 57357, Cairo 11441, Egypt.
Mustafa Shaban ShawkyPathology Department, Children's Cancer Hospital Egypt 57357, Cairo 11441, Egypt.
Manal ZamzamPediatric Oncology Department, Children's Cancer Hospital Egypt 57357, Cairo 11441, Egypt.
Iman ZakyRadio Diagnosis Department, Children's Cancer Hospital Egypt 57357, Cairo 11441, Egypt.
Ahmed ElghounimyMusculoskeletal Tumor Surgery Unit, Children's Cancer Hospital Egypt 57357, Cairo 11441, Egypt.ORCID 0000-0003-2105-8749
Shahenda El-NaggarTumor Biology Research Program, Basic Research Unit, Research Department, Children's Cancer Hospital Egypt 57357, Cairo 11441, Egypt.ORCID 0000-0001-6465-9881
Sameh MagdeldinProteomics and Metabolomics Research Program, Basic Research Unit, Research Department, Children's Cancer Hospital Egypt 57357, Cairo 11441, Egypt.ORCID 0000-0002-7507-9935

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma is a primary malignant bone tumor affecting adolescents and young adults. This study aimed to identify proteomic signatures that distinguish between different osteosarcoma subtypes, providing insights into their molecular heterogeneity and potential implications for personalized treatment approaches. Using advanced proteomic techniques, we analyzed FFPE tumor samples from a cohort of pediatric osteosarcoma patients representing four various subtypes. Differential expression analysis revealed a significant proteomic signature that discriminated between these subtypes, highlighting distinct molecular profiles associated with different tumor characteristics. In contrast, clinical determinants did not correlate with the proteome signature of pediatric osteosarcoma. The identified proteomics signature encompassed a diverse array of proteins involved in focal adhesion, ECM-receptor interaction, PI3K-Akt signaling pathways, and proteoglycans in cancer, among the top enriched pathways. These findings underscore the importance of considering the molecular heterogeneity of osteosarcoma during diagnosis or even when developing personalized treatment strategies. By identifying subtype-specific proteomics signatures, clinicians may be able to tailor therapy regimens to individual patients, optimizing treatment efficacy and minimizing adverse effects.

Indexed as

Bone NeoplasmsOsteosarcomaAdolescentChildHumansPhosphatidylinositol 3-KinasesProteoglycansProteomicsYoung AdultPhosphatidylinositol 3-KinasesProteoglycansosteosarcomapediatric cancerproteomics

Identifiers

PMID37681913
PMCPMC10487120

What Socratic 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 Socratic graph.