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Targeting Lysyl Oxidase Family Meditated Matrix Cross-Linking as an Anti-Stromal Therapy in Solid Tumours
Yordanos F I Setargew1, Kaitlin Wyllie1, Rhiannon D Grant1
1The Garvan Institute of Medical Research and The Kinghorn Cancer Centre, Darlinghurst, NSW 2010, Australia.
Abstract:
The lysyl oxidase (LOX) family of enzymes are a major driver in the biogenesis of desmoplastic matrix at the primary tumour and secondary metastatic sites. With the increasing interest in and development of anti-stromal therapies aimed at improving clinical outcomes of cancer patients, the Lox family has emerged as a potentially powerful clinical target. This review examines how lysyl oxidase family dysregulation in solid cancers contributes to disease progression and poor patient outcomes, as well as an evaluation of the preclinical landscape of LOX family targeting therapeutics. We also discuss the suitability of the LOX family as a diagnostic and/or prognostic marker in solid tumours.
Insights
The lysyl oxidase (LOX) enzyme family drives tumor matrix formation and metastasis. Targeting LOX enzymes offers a promising therapeutic strategy for cancer, with potential as diagnostic and prognostic markers.
Area of Science:
- Oncology
- Biochemistry
- Cancer Biology
Background:
- The lysyl oxidase (LOX) enzyme family is crucial for desmoplastic matrix formation in primary tumors and metastatic sites.
- Dysregulation of LOX enzymes contributes significantly to cancer progression and adverse patient outcomes.
Purpose of the Study:
- To review the role of LOX family dysregulation in solid cancers.
- To evaluate the preclinical therapeutic landscape targeting the LOX family.
- To discuss the potential of LOX enzymes as diagnostic and prognostic markers.
Main Methods:
- Literature review of studies on LOX enzymes in cancer.
- Analysis of preclinical data for LOX-targeting therapeutics.
- Evaluation of LOX family's role in tumor microenvironment and metastasis.
Main Results:
- LOX family enzymes are key drivers of desmoplastic matrix, promoting tumor growth and metastasis.
- Targeting LOX family enzymes is a developing strategy in anti-stromal cancer therapies.
- LOX family members show potential as biomarkers for cancer diagnosis and prognosis.
Conclusions:
- LOX family dysregulation is a critical factor in solid tumor progression and poor prognosis.
- Therapeutic targeting of LOX enzymes represents a promising avenue for improving cancer patient outcomes.
- The LOX family holds potential as valuable diagnostic and prognostic indicators in oncology.
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