YAP/TAZ Related BioMechano Signal Transduction and Cancer Metastasis

Mechanoreciprocity refers to a cell’s ability to maintain tensional homeostasis in response to various types of forces. Physical forces are continually being exerted upon cells of various tissue types, even those considered static, such as the brain. Through mechanoreceptors, cells sense and subsequently respond to these stimuli. These forces and their respective cellular responses are prevalent in regulating everything from embryogenic tissue-specific differentiation, programmed cell death, and disease progression, the last of which being the subject of extensive attention. Abnormal mechanical remodeling of cells can provide clues as to the pathological status of tissues. This becomes particularly important in cancer cells, where cellular stiffness has been recently accepted as a novel biomarker for cancer metastasis. Several studies have also elucidated the importance of cell stiffness in cancer metastasis, with data highlighting that a reversal of tumor stiffness has the capacity to revert the metastatic properties of cancer. In this review, we summarize our current understanding of extracellular matrix (ECM) homeostasis, which plays a prominent role in tissue mechanics. We also describe pathological disruption of the ECM, and the subsequent implications toward cancer and cancer metastasis. In addition, we highlight the most novel approaches toward understanding the mechanisms which generate pathogenic cell stiffness and provide potential new strategies which have the capacity to advance our understanding of one of human-kinds’ most clinically significant medical pathologies. These new strategies include video-based techniques for structural dynamics, which have shown great potential for identifying full-field, high-resolution modal properties, in this case, as a novel application.

[1]  M. Mushtaq,et al.  Tumor matrix remodeling and novel immunotherapies: the promise of matrix-derived immune biomarkers , 2018, Journal of Immunotherapy for Cancer.

[2]  G. Comi,et al.  Rhabdomyolysis-Associated Acute Kidney Injury. , 2018, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[3]  R. Giles,et al.  TCF21 hypermethylation regulates renal tumor cell clonogenic proliferation and migration , 2017, Molecular oncology.

[4]  Peter Friedl,et al.  Mechanoreciprocity in cell migration , 2017, Nature Cell Biology.

[5]  D. Navajas,et al.  Force Triggers YAP Nuclear Entry by Regulating Transport across Nuclear Pores , 2017, Cell.

[6]  G. Calamita,et al.  Bile Acids and Cancer: Direct and Environmental-Dependent Effects. , 2017, Annals of hepatology.

[7]  Caroline L. Wilson,et al.  Epigenetic reprogramming in liver fibrosis and cancer☆ , 2017, Advanced drug delivery reviews.

[8]  Y. Teo,et al.  Genome-wide association study identified copy number variants associated with sporadic colorectal cancer risk , 2017, Journal of Medical Genetics.

[9]  E. Charlaix,et al.  Noncontact Viscoelastic Imaging of Living Cells Using a Long-Needle Atomic Force Microscope with Dual-Frequency Modulation , 2017 .

[10]  Joe Gray,et al.  Combinatorial Microenvironments Impose a Continuum of Cellular Responses to a Single Pathway-Targeted Anti-cancer Compound. , 2017, Cell reports.

[11]  S. Piccolo,et al.  Mechanobiology of YAP and TAZ in physiology and disease , 2017, Nature Reviews Molecular Cell Biology.

[12]  S. Karim,et al.  Matrix stiffness induces epithelial–mesenchymal transition and promotes chemoresistance in pancreatic cancer cells , 2017, Oncogenesis.

[13]  S. Karim,et al.  Substrate Rigidity Controls Activation and Durotaxis in Pancreatic Stellate Cells , 2017, Scientific Reports.

[14]  V. Weaver,et al.  Extracellular Matrix Remodeling and Stiffening Modulate Tumor Phenotype and Treatment Response , 2017 .

[15]  M. Sudol,et al.  Framework to function: mechanosensitive regulators of gene transcription , 2016, Cellular & Molecular Biology Letters.

[16]  S. Chien,et al.  Flow-dependent YAP/TAZ activities regulate endothelial phenotypes and atherosclerosis , 2016, Proceedings of the National Academy of Sciences.

[17]  S. Piccolo,et al.  YAP/TAZ as therapeutic targets in cancer. , 2016, Current opinion in pharmacology.

[18]  Jongshin Kim,et al.  Actin remodeling confers BRAF inhibitor resistance to melanoma cells through YAP/TAZ activation , 2016, The EMBO journal.

[19]  A. Bergh,et al.  Inhibition of Lysyl Oxidase and Lysyl Oxidase-Like Enzymes Has Tumour-Promoting and Tumour-Suppressing Roles in Experimental Prostate Cancer , 2016, Scientific Reports.

[20]  J. Erler,et al.  Lysyl Oxidase, a Targetable Secreted Molecule Involved in Cancer Metastasis. , 2016, Cancer research.

[21]  Deyu Li,et al.  YAP overexpression promotes the epithelial-mesenchymal transition and chemoresistance in pancreatic cancer cells. , 2016, Molecular medicine reports.

[22]  N. Carragher,et al.  ADF and Cofilin1 Control Actin Stress Fibers, Nuclear Integrity, and Cell Survival , 2015, Cell reports.

[23]  J. Xiang,et al.  Role of cellular cytoskeleton in epithelial-mesenchymal transition process during cancer progression. , 2015, Biomedical reports.

[24]  Albert C. Chen,et al.  Matrix stiffness drives Epithelial-Mesenchymal Transition and tumour metastasis through a TWIST1-G3BP2 mechanotransduction pathway , 2015, Nature Cell Biology.

[25]  Pinhas Girshovitz,et al.  Optical‐mechanical signatures of cancer cells based on fluctuation profiles measured by interferometry , 2014, Journal of biophotonics.

[26]  F. Vizoso,et al.  Expression and prognostic significance of fibronectin and matrix metalloproteases in breast cancer metastasis , 2014, Histopathology.

[27]  N. Elvassore,et al.  A Mechanical Checkpoint Controls Multicellular Growth through YAP/TAZ Regulation by Actin-Processing Factors , 2013, Cell.

[28]  Ricardo Garcia,et al.  Nanomechanical mapping of soft matter by bimodal force microscopy , 2013 .

[29]  S. Weiss,et al.  MT1-MMP-dependent control of skeletal stem cell commitment via a β1-integrin/YAP/TAZ signaling axis. , 2013, Developmental cell.

[30]  Thomas R. Cox,et al.  The rationale for targeting the LOX family in cancer , 2012, Nature Reviews Cancer.

[31]  Ning Wang,et al.  Intrinsically high-Q dynamic AFM imaging in liquid with a significantly extended needle tip , 2012, Nanotechnology.

[32]  Taeck J Jeon,et al.  Regulation of actin cytoskeleton by Rap1 binding to RacGEF1 , 2012, Molecules and cells.

[33]  F. Sotgia,et al.  Caveolin-1 and cancer metabolism in the tumor microenvironment: markers, models, and mechanisms. , 2012, Annual review of pathology.

[34]  Alexandra Naba,et al.  Overview of the matrisome--an inventory of extracellular matrix constituents and functions. , 2012, Cold Spring Harbor perspectives in biology.

[35]  E. Diamanti-Kandarakis,et al.  Phenotypes and enviromental factors: their influence in PCOS. , 2012, Current pharmaceutical design.

[36]  Daniel J Müller,et al.  Atomic force microscopy: a nanoscopic window on the cell surface. , 2011, Trends in cell biology.

[37]  Nicola Elvassore,et al.  Role of YAP/TAZ in mechanotransduction , 2011, Nature.

[38]  Thomas R. Cox,et al.  Remodeling and homeostasis of the extracellular matrix: implications for fibrotic diseases and cancer , 2011, Disease Models & Mechanisms.

[39]  M. Allen,et al.  Jekyll and Hyde: the role of the microenvironment on the progression of cancer , 2011, The Journal of pathology.

[40]  Y. Sugawara,et al.  Simultaneous observation of surface topography and elasticity at atomic scale by multifrequency frequency modulation atomic force microscopya) , 2010 .

[41]  Leonard J Foster,et al.  Pseudopodial actin dynamics control epithelial-mesenchymal transition in metastatic cancer cells. , 2010, Cancer research.

[42]  Mikala Egeblad,et al.  Matrix Crosslinking Forces Tumor Progression by Enhancing Integrin Signaling , 2009, Cell.

[43]  Richard O. Hynes,et al.  The Extracellular Matrix: Not Just Pretty Fibrils , 2009, Science.

[44]  M. Nugent,et al.  Lysyl Oxidase Pro-peptide Inhibits Prostate Cancer Cell Growth by Mechanisms that Target FGF-2-Cell Binding and Signaling , 2009, Oncogene.

[45]  David J. Mooney,et al.  Growth Factors, Matrices, and Forces Combine and Control Stem Cells , 2009, Science.

[46]  Raghu Kalluri,et al.  The basics of epithelial-mesenchymal transition. , 2009, The Journal of clinical investigation.

[47]  R. Boot-Handford,et al.  Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations , 2009, Nature Reviews Genetics.

[48]  Valerie M. Weaver,et al.  A tense situation: forcing tumour progression , 2009, Nature Reviews Cancer.

[49]  Jan Lammerding,et al.  Mechanotransduction gone awry , 2009, Nature Reviews Molecular Cell Biology.

[50]  Robert A. Weinberg,et al.  Epithelial-mesenchymal transition: at the crossroads of development and tumor metastasis. , 2008, Developmental cell.

[51]  M. Krieg,et al.  Tensile forces govern germ-layer organization in zebrafish , 2008, Nature Cell Biology.

[52]  S. Chizhik,et al.  Atomic force microscopy probing of cell elasticity. , 2007, Micron.

[53]  M. Hendrix,et al.  Paradoxical roles for lysyl oxidases in cancer—A prospect , 2007, Journal of cellular biochemistry.

[54]  Andrew J. Ewald,et al.  Matrix metalloproteinases and the regulation of tissue remodelling , 2007, Nature Reviews Molecular Cell Biology.

[55]  V. Brower Researchers tackle metastasis, cancer's last frontier. , 2007, Journal of the National Cancer Institute.

[56]  A. Aszódi,et al.  What mouse mutants teach us about extracellular matrix function. , 2006, Annual review of cell and developmental biology.

[57]  Roger Proksch,et al.  Multifrequency, repulsive-mode amplitude-modulated atomic force microscopy , 2006 .

[58]  S. Sen,et al.  Matrix Elasticity Directs Stem Cell Lineage Specification , 2006, Cell.

[59]  D. Steindler,et al.  Mesenchymal Stem Cells Spontaneously Express Neural Proteins in Culture and Are Neurogenic after Transplantation , 2006, Stem cells.

[60]  Emilios Tahinci,et al.  Migrating anterior mesoderm cells and intercalating trunk mesoderm cells have distinct responses to Rho and Rac during Xenopus gastrulation , 2006, Developmental dynamics : an official publication of the American Association of Anatomists.

[61]  M. Sheetz,et al.  Local force and geometry sensing regulate cell functions , 2006, Nature Reviews Molecular Cell Biology.

[62]  Cynthia A. Reinhart-King,et al.  Tensional homeostasis and the malignant phenotype. , 2005, Cancer cell.

[63]  J. Peterse,et al.  Breast cancer metastasis: markers and models , 2005, Nature Reviews Cancer.

[64]  M. R. Mozafari,et al.  A review of scanning probe microscopy investigations of liposome-DNA complexes. , 2005 .

[65]  Matthew J. Paszek,et al.  The Tension Mounts: Mechanics Meets Morphogenesis and Malignancy , 2004, Journal of Mammary Gland Biology and Neoplasia.

[66]  Ricardo Garcia,et al.  Compositional mapping of surfaces in atomic force microscopy by excitation of the second normal mode of the microcantilever , 2004 .

[67]  E. Farge Mechanical Induction of Twist in the Drosophila Foregut/Stomodeal Primordium , 2003, Current Biology.

[68]  M. Hendrix,et al.  A molecular role for lysyl oxidase in breast cancer invasion. , 2002, Cancer research.

[69]  H. Haga,et al.  Drastic change of local stiffness distribution correlating to cell migration in living fibroblasts. , 2001, Cell motility and the cytoskeleton.

[70]  D. Hanahan,et al.  The Hallmarks of Cancer , 2000, Cell.

[71]  Z. Stachura,et al.  Elasticity of normal and cancerous human bladder cells studied by scanning force microscopy , 1999, European Biophysics Journal.