Target intelligence / Profile preview

Suppressor of tumorigenicity 7 protein-like (ST7L)

Target
ST7L
Molecular classification
Other (protein-coding, tumor suppressor), Not an enzyme, receptor, ion channel, or transporter, No evidence of being a G protein-coupled receptor, transcription factor, or histone modifier
01

Overview

Suppressor of tumorigenicity 7 protein-like (ST7L) is a gene product identified by its similarity to the ST7 tumor suppressor gene. It is clustered near WNT2B on the chromosome and frequently found to be downregulated in various cancers. ST7L exerts potent antitumor functions, suppressing cell proliferation, migration, and invasion by inhibiting Wnt/β-catenin signaling. Overexpression of ST7L increases cell adhesion molecules such as E-cadherin and reduces markers of EMT, thus restricting cancer cell metastatic potential. Although no drugs directly target ST7L, it represents an important molecule for future cancer therapy development.

Other names
ST7LSuppressor of tumorigenicity 7 protein-likeST7-related proteinFAM4BSTLRST7RFLJ20284
02

Mechanism of action

For potential drugs: restoration of ST7L function may suppress Wnt/β-catenin signaling, resulting in anti-tumor effects. Targeting pathways that modulate ST7L expression (e.g., miR-23a inhibits ST7L, reducing tumor suppressor activity). Indirect mechanisms via RNA interference or gene therapy (potential/future research).

03

Biological functions

Cell proliferation inhibitionCell invasion suppressionRestriction of epithelial-mesenchymal transition (EMT) in cancer cellsModulation of Wnt/β-catenin signalingRegulation of cell cycle progression (increase in G1 phase, decrease in S phase)No direct evidence for apoptosis induction
04

Disease associations

Cancer (notably breast cancer, epithelial ovarian cancer, gastric cancer, glioma)Tumor suppressor activity; downregulation associated with increased tumorigenesis
05

Safety considerations

No direct therapeutic safety concerns reported for ST7L targeting.As with most tumor suppressor gene restoration strategies, general risks relate to off-target effects or immune response to gene therapies.
06

Interacting drugs

None currently known
07

Biomarkers

ST7L downregulation in tumors may serve as a biomarker of malignancy in breast, ovarian, gastric, and glioma cancersmiR-23a (which downregulates ST7L) as a potential biomarker for poor prognosis

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