Target intelligence / Profile preview

Leucine zipper tumor suppressor 2 (LZTS2)

Target
LZTS2
Molecular classification
Tumor suppressor, Transcription regulator, Negative regulator of Wnt/β-catenin signaling, Leucine zipper protein, Other (microtubule regulator)
01

Overview

Leucine zipper tumor suppressor 2 (LZTS2) is a member of the leucine zipper tumor suppressor family, encoded by a gene located at chromosome 10q24.3—a locus frequently lost in diverse human tumors[1][2][4]. The LZTS2 protein contains a leucine zipper domain and a nuclear export signal, enabling interaction with and regulation of β-catenin, a critical mediator of Wnt signaling. LZTS2 negatively regulates β-catenin-mediated transcription, inhibits the Wnt signaling pathway, controls cell-cycle progression, and is required for cytokinesis through microtubule regulation[1][4]. Its tumor suppressor role is linked to repression of cell proliferation and prevention of tumorigenesis. Aberrant methylation and altered expression of LZTS2 have diagnostic and prognostic implications in cancer, especially liver and stomach cancers, where its expression can be modulated by epigenetic regulation[3][4]. Some compounds (including acetaminophen and environmental chemicals) are predicted to influence its expression, but no clinically established drugs target it directly.

Other names
Leucine zipper putative tumor suppressor 2KIAA1813LAPSER1hLZTS2Protein LAPSER1
02

Mechanism of action

Epigenetic modulation (e.g., methylation status) may affect gene expression[3]; Drugs potentially influence LZTS2 expression but direct mechanism of action in therapy not established[3]

03

Biological functions

Regulation of cell cycleNegative regulation of β-catenin-mediated transcriptionNegative regulation of Wnt signaling pathwayRepression of cell proliferationCentral spindle formation and cytokinesisRegulation of microtubule severing
04

Disease associations

Cancer
05

Safety considerations

None documented specifically for LZTS2-targeted therapy; general tumor suppressor targeting concerns include risk of unanticipated effects on normal cell-cycle regulation
06

Interacting drugs

1,2-Dimethylhydrazine

2 more in the full profile.

07

Biomarkers

LZTS2 methylation (pan-cancer diagnostic or prognostic biomarker, notably in liver and gastric cancer)[3]

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