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Updated: May 18, 2026

Induction and Analysis of Epithelial to Mesenchymal Transition
Published on: August 27, 2013
LOXL2 in epithelial cell plasticity and tumor progression
Amparo Cano1, Patricia G Santamaría, Gema Moreno-Bueno
1Departamento de Bioquímica, UAM, Instituto de Investigaciones Biomédicas Alberto Sols CSIC-UAM, IdiPAZ, Arzobispo Morcillo, 2, 28029 Madrid, Spain. acano@iib.uam.es
Lysyl oxidase-like 2 (LOXL2) impacts tumor progression and metastasis through extracellular matrix remodeling and intracellular functions. Intracellular LOXL2 expression correlates with poor prognosis and metastasis in certain cancers, suggesting therapeutic potential.
Area of Science:
- Molecular Biology
- Cancer Biology
- Biochemistry
Background:
- Lysyl oxidase family members regulate tumor progression.
- LOXL2 is implicated in the progression and metastasis of various cancers, including breast carcinomas.
- LOXL2 exhibits both secreted functions in extracellular matrix remodeling and intracellular roles.
Purpose of the Study:
- To review the multifaceted roles of LOXL2 in cancer.
- To highlight the significance of intracellular LOXL2 expression in tumor progression and metastasis.
- To explore the therapeutic implications of LOXL2's functions.
Main Methods:
- Literature review of studies on LOXL2.
- Analysis of LOXL2's extracellular matrix remodeling functions.
- Investigation of LOXL2's intracellular regulatory mechanisms, including transcriptional repression.
Main Results:
- Secreted LOXL2 remodels the tumor microenvironment's extracellular matrix.
- Intracellular LOXL2 regulates epithelial-to-mesenchymal transition, cell polarity, and differentiation.
- Intracellular (perinuclear) LOXL2 expression is linked to poor prognosis and distant metastasis in specific cancers like larynx squamous cell carcinoma and basal breast carcinomas.
Conclusions:
- LOXL2 possesses diverse functions critical to tumor progression.
- Intracellular LOXL2 localization is a significant prognostic indicator.
- Targeting LOXL2 presents a promising therapeutic strategy for cancer treatment.
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