Target intelligence / Profile preview

Serum amyloid A-like protein 1 (SAAL1)

Target
SAAL1
Molecular classification
Other (amino acid/protein, non-enzymatic, non-receptor), Serum amyloid A protein superfamily
01

Overview

Serum amyloid A-like protein 1 (SAAL1) is a 474-amino acid acidic protein (approximate mass 54 kDa) encoded by the SAAL1 gene on chromosome 11p15.1. SAAL1 belongs to the serum amyloid A superfamily but is a distinct gene and protein from classic acute-phase serum amyloid A isoforms. SAAL1 is ubiquitously expressed at moderate levels, with highest levels in testis, and is present in both nuclear and cytoplasmic compartments depending on cell type. It is functionally important in promoting the proliferation and cell cycle progression of synovial fibroblasts under inflammatory conditions, and its overexpression is associated with pathogenesis in rheumatoid arthritis and osteoarthritis, as well as in the progression and poor prognosis of several human cancers, including hepatocellular carcinoma. Mechanistically, SAAL1 mediates G1/S transition by stabilizing CDK6 mRNA and is implicated in inflammation-associated cell cycle regulation and tumorigenesis. Pan-cancer analyses suggest that high SAAL1 expression may predict an immune-inflamed tumor phenotype and potentially enhanced response to immunotherapies. SAAL1 also interacts with several viral proteins and immunity-regulating proteins, suggesting broader roles in host defense and innate immunity.

Other names
SAAL1SPACIA1Synoviocyte proliferation-associated in collagen-induced arthritis protein 1Synoviocyte proliferation-associated in collagen-induced arthritis 1serum amyloid A like 1
02

Mechanism of action

No direct targeting drugs described. Modulation of SAAL1 (e.g., by siRNA knockdown) affects cell proliferation and migration, increases sensitivity to kinase inhibitors like sorafenib and foretinib in cancer models

03

Biological functions

Promotes proliferation of synovial fibroblasts, especially in inflammatory and arthritic conditionsRegulates cell cycle via stabilization of CDK6 mRNAModulates cell cycle progression (G1/S transition)Influences cell migration (notably in hepatocellular carcinoma)May act as an interferon stimulator and interact with innate immunity pathwaysShown to interact with multiple viral proteins (e.g., SARS-CoV-2, influenza)
04

Disease associations

Cancer (notably hepatocellular carcinoma, pan-cancer contexts)Rheumatoid and osteoarthritic inflammationPotential broader roles in infectious disease and immune responses
05

Safety considerations

No specific toxicity or safety concerns documented for targeting SAAL1 directly, but its influence on cell proliferation and immune responses suggests attention to potential effects on normal tissue homeostasis and host defense
06

Interacting drugs

Sorafenib (sensitivity increased by SAAL1 knockdown in HCC cells)

1 more in the full profile.

07

Biomarkers

SAAL1 expression in tumors may correlate with immune-activated (immune-inflamed) tumor microenvironments and could aid in predicting response to immune checkpoint blockade therapiesSAAL1 overexpression may serve as a biomarker for synovial fibroblast proliferation or disease progression in some arthritis subtypes

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