The Biological and Biomechanical Role of Transglutaminase-2 in the Tumour Microenvironment.
Robert TempestSonia GuarnerioRawan MaaniJamie CooperNicholas PeakePublished in: Cancers (2021)
Transglutaminase-2 (TG2) is the most highly and ubiquitously expressed member of the transglutaminase enzyme family and is primarily involved in protein cross-linking. TG2 has been implicated in the development and progression of numerous cancers, with a direct role in multiple cellular processes and pathways linked to apoptosis, chemoresistance, epithelial-mesenchymal transition, and stem cell phenotype. The tumour microenvironment (TME) is critical in the formation, progression, and eventual metastasis of cancer, and increasing evidence points to a role for TG2 in matrix remodelling, modulation of biomechanical properties, cell adhesion, motility, and invasion. There is growing interest in targeting the TME therapeutically in response to advances in the understanding of its critical role in disease progression, and a number of approaches targeting biophysical properties and biomechanical signalling are beginning to show clinical promise. In this review we aim to highlight the wide array of processes in which TG2 influences the TME, focussing on its potential role in the dynamic tissue remodelling and biomechanical events increasingly linked to invasive and aggressive behaviour. Drug development efforts have yielded a range of TG2 inhibitors, and ongoing clinical trials may inform strategies for targeting the biomolecular and biomechanical function of TG2 in the TME.
Keyphrases
- stem cells
- finite element analysis
- epithelial mesenchymal transition
- finite element
- clinical trial
- cancer therapy
- cell adhesion
- oxidative stress
- high throughput
- squamous cell carcinoma
- drug delivery
- endoplasmic reticulum stress
- big data
- randomized controlled trial
- transforming growth factor
- cell proliferation
- escherichia coli
- signaling pathway
- pseudomonas aeruginosa
- cell therapy
- artificial intelligence
- pi k akt
- cystic fibrosis
- mesenchymal stem cells
- protein protein