# SAA1 Protein: A Potential Biomarker for Acute Myeloid Leukemia

**Authors:** Pedro Leite Azevedo, Mayara Rezende, Milena Felix, Stephany Corrêa, Eliana Abdelhay, Renata Binato

PMC · DOI: 10.3390/biomedicines13040880 · Biomedicines · 2025-04-05

## TL;DR

This study identifies SAA1 as a potential biomarker for diagnosing acute myeloid leukemia, highlighting its role in inflammation and immune signaling.

## Contribution

The study introduces SAA1 as a novel potential biomarker for AML diagnosis based on proteomic and ELISA findings.

## Key findings

- Proteomic analysis identified 36 differentially expressed proteins in AML patient plasma, including SAA1.
- SAA1 expression was confirmed via ELISA and linked to immune signaling through NF-kappa-B activation.
- SAA1 is proposed as a promising biomarker for AML diagnosis.

## Abstract

Background/Objectives: Despite its heterogeneity and diagnostic challenges, acute myeloid leukemia (AML) originates from stem cell transformation and alterations in the hematopoietic niche (HN) could be related to leukemic transformation. Therefore, the aim of this study was to evaluate the protein profile of HN from AML patients and compare it with the profile of healthy donors (HDs). Methods: A proteomic analysis was conducted to identify differentially expressed (DE) proteins in BM plasma from AML patients and HD. In silico analysis was performed to identify biological processes and signaling pathways involved. Additionally, ELISA confirmed the expression of the DE protein of interest in BM plasma samples. Results: Proteomic analysis revealed alterations in the plasma profiles of AML patients and 36 DE proteins were found. Among then, we highlight C8G, CFB, SAA1, SERPINA3 and SERPINC1, which are related to inflammatory response process. Thus, considering the role of the secreted protein SAA1 in the inflammatory context and that it is described as a potential biomarker in several tumors, we selected SAA1 for ELISA confirmation. The results corroborated our findings, indicating that increased expression of SAA1 could be related to AML. Our results also revealed that SAA1 can stimulate immune signaling through NF-kappa-B activation. Conclusions: These findings position SAA1 as a promising biomarker for AML diagnosis, offering a potential tool for more accurate identification of the disease. Nevertheless, further studies are needed to understand the relationship of SAA1 with the leukemic transformation process in AML and its potential clinical use.

## Linked entities

- **Proteins:** SAA1 (serum amyloid A1), C8G (complement C8 gamma chain), CFB (complement factor B), SERPINA3 (serpin family A member 3), SERPINC1 (serpin family C member 1)
- **Diseases:** acute myeloid leukemia (MONDO:0015667), AML (MONDO:0018874)

## Full-text entities

- **Genes:** SERPINC1 (serpin family C member 1) [NCBI Gene 462] {aka AT3, AT3D, ATIII, ATIII-R2, ATIII-T1, ATIII-T2}, SAA1 (serum amyloid A1) [NCBI Gene 6288] {aka PIG4, SAA, TP53I4}, CFB (complement factor B) [NCBI Gene 629] {aka AHUS4, ARMD14, BF, BFD, CFAB, CFBD}, SERPINA3 (serpin family A member 3) [NCBI Gene 12] {aka AACT, ACT, GIG24, GIG25}, C8G (complement C8 gamma chain) [NCBI Gene 733] {aka C8C}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}
- **Diseases:** HD (MESH:D006816), inflammatory (MESH:D007249), leukemic (MESH:D007938), tumors (MESH:D009369), AML (MESH:D015470)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12024993/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12024993/full.md

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Source: https://tomesphere.com/paper/PMC12024993