Target intelligence / Profile preview

Complement C1q-like protein 4 (C1QL4)

Target
C1QL4
Molecular classification
Secreted protein, C1q/TNF superfamily, Adiponectin paralog, Other
01

Overview

Complement C1q-like protein 4 (**C1QL4**) is a secreted member of the C1q/TNF superfamily, structurally related to complement C1q and adiponectin family proteins. It is encoded by the C1QTNF11 gene and is also known as CTRP11. C1QL4 contains a characteristic C1q domain forming trimers, involved in protein-protein interactions and signaling. Functionally, C1QL4 binds to cell-surface receptors such as BAI3 (brain-specific angiogenesis inhibitor 3), regulating cell differentiation processes like myoblast fusion by acting as a negative regulator[2]. In cancer biology, C1QL4 promotes breast cancer cell stemness and drives epithelial-mesenchymal transition (EMT) through modulation of the PI3K/AKT/NF-κB signaling axis, correlating with poor prognosis and increased metastatic potential in breast cancer[4]. While detailed pharmacological targeting has not been described, its involvement in key regulatory cell pathways positions C1QL4 as a candidate therapeutic target in oncology and regenerative medicine[4][2][3].

Other names
C1QL4Complement C1q-like protein 4CTRP11C1q/TNF-related protein 11C1QTNF11Complement component 1, q subcomponent-like 4
02

Mechanism of action

Not established for drugs, but C1QL4 acts as a ligand for cell-surface receptors like BAI3, modulating downstream signaling pathways involved in cancer and tissue differentiation[2][4].

03

Biological functions

Regulation of cell differentiation (e.g., inhibition of myoblast fusion)Modulation of cell signaling pathways (e.g., PI3K/AKT/NF-κB)Regulation of cancer cell stemness and epithelial-mesenchymal transition (EMT)Synaptic and neural development (by analogy to other C1QL proteins)Other
04

Disease associations

Cancer (notably breast cancer)Other (potential roles in cell fusion and neurobiology)
05

Safety considerations

As a potential therapeutic target, modulation might impact cellular differentiation, cancer metastasis, and normal tissue development due to roles in EMT and stemness[4]
06

Biomarkers

High expression correlated with poor prognosis in breast cancer (potential biomarker for metastatic risk and cancer stem cell properties)[4]

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