Target intelligence / Profile preview

Latexin (LXN) (LXN)

Target
LXN
Molecular classification
Carboxypeptidase inhibitor, Tumor suppressor
01

Overview

Latexin (LXN) is a highly conserved protein and the only known endogenous inhibitor of zinc-dependent metallocarboxypeptidases, such as carboxypeptidase A (CPA1, CPA2, CPA4) and B (CPB1), in mammals [11]. It plays a critical role as a tumor suppressor, with its expression frequently lost or downregulated through promoter hypermethylation in various cancers, including leukemia, lymphoma, and gastric and prostate carcinomas [2, 8, 11]. In addition to its role in oncology, latexin is a key homeostatic regulator of the hematopoietic stem cell (HSC) pool, where it limits stem cell self-renewal and promotes apoptosis [8, 9]. Its expression is also linked to inflammatory responses, particularly in mast cells, and it serves as a marker for specific neuronal populations in the brain [2, 9]. Although no direct small-molecule inhibitors or activators of latexin are currently in clinical use, its potential as a therapeutic target is being explored, with studies showing that its expression can be modulated by agents like retinoic acid and DNA methyltransferase inhibitors [4, 8].

Other names
LXNEndogenous carboxypeptidase inhibitorECP-ITissue carboxypeptidase inhibitorTCIMUM
02

Mechanism of action

Latexin acts as a non-competitive inhibitor of zinc-dependent metallocarboxypeptidases, including CPA1, CPA2, and CPA4 [11]. It functions as a tumor suppressor by downregulating anti-apoptotic genes such as Bcl-2 and Pim-2 and negatively regulating the self-renewal of hematopoietic stem cells [8, 9].

03

Biological functions

Inhibition of carboxypeptidase ARegulation of hematopoietic stem cell populationTumor suppressionApoptosis inductionInflammation regulation
04

Disease associations

CancerLeukemiaLymphomaProstate cancerGastric cancerInflammation
05

Safety considerations

Potential impairment of hematopoietic stem cell homeostasisSystemic toxicity from broad carboxypeptidase inhibition
06

Interacting drugs

All-trans retinoic acid

1 more in the full profile.

07

Biomarkers

Latexin expression levelLatexin promoter methylation status

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