Comparative Shotgun Proteomics Reveals the Characteristic Protein Signature of Osteosarcoma Subtypes

Author:

Alaa Maram1,Al-Shehaby Nouran2,Anwar Ali Mostafa3,Farid Nesma4,Shawky Mustafa Shaban5,Zamzam Manal67,Zaky Iman89,Elghounimy Ahmed101112ORCID,El-Naggar Shahenda2ORCID,Magdeldin Sameh313ORCID

Affiliation:

1. Immunology and Microbiology Research Program, Basic Research Unit, Research Department, Children’s Cancer Hospital Egypt 57357, Cairo 11441, Egypt

2. Tumor Biology Research Program, Basic Research Unit, Research Department, Children’s Cancer Hospital Egypt 57357, Cairo 11441, Egypt

3. Proteomics and Metabolomics Research Program, Basic Research Unit, Research Department, Children’s Cancer Hospital Egypt 57357, Cairo 11441, Egypt

4. Clinical Research Unit, Research Department, Children’s Cancer Hospital Egypt 57357, Cairo 11441, Egypt

5. Pathology Department, Children’s Cancer Hospital Egypt 57357, Cairo 11441, Egypt

6. Pediatric Oncology Department, Children’s Cancer Hospital Egypt 57357, Cairo 11441, Egypt

7. Pediatric Oncology Department, National Cancer Institute, Cairo University, Cairo 12613, Egypt

8. Radio Diagnosis Department, Children’s Cancer Hospital Egypt 57357, Cairo 11441, Egypt

9. Radio Diagnosis Department, National Cancer Institute, Cairo University, Cairo 12613, Egypt

10. Musculoskeletal Tumor Surgery Unit, Children’s Cancer Hospital Egypt 57357, Cairo 11441, Egypt

11. Department of Orthopedic Surgery, Faculty of Medicine, Cairo University, Cairo 12613, Egypt

12. Regenerative Medicine Research Program, Basic Research Unit, Research Department, Children’s Cancer Hospital Egypt 57357, Cairo 11441, Egypt

13. Department of Physiology, Faculty of Veterinary Medicine, Suez Canal University, Ismailia 41522, Egypt

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.

Funder

Egypt Cancer Network, USA

Children’s Cancer Hospital, Egypt 57357

Publisher

MDPI AG

Subject

General Medicine

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