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.

Cancers
|January 30, 2021
PubMed

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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