Growth factors in tumor microenvironment
Xuejing Zhang, Daotai Nie, Subhas Chakrabarty
SimmonCooper Cancer Institute, Southern Illinois University School of Medicine
TABLE OF CONTENTS
- 1. Abstract
- 2. Introduction
- 3. Epidermal Growth Factor and Receptor in Tumor Microenvironment
- 3.1. Epidermal growth factor and epidermal growth factor receptor
- 3.2. Tumor hypoxia and translational up-regulation of epidermal growth factor receptor
- 3.2.1. The hypoxic tumor microenvironment triggers the expression of epidermal growth factor receptor
- 3.2.2. The role of epidermal growth factor receptor in hypoxia-mediated tumor progression
- 3.3. Role of epidermal growth factor receptor in the Pathogenesis of Metastasis
- 3.3.1. The direct role of epidermal growth factor receptor in stimulating osteoclast
- 3.3.2. Epidermal growth factor receptor in mesenchymal stem cell-mediated osteoclast differentiation
- 3.4. EGFR signaling regulated by tumor microenvironment
- 4. Fibroblast Growth Factor amd Receptor in Tumor Microenvironment
- 4.1. Fibroblast growth factor and fibroblast growth factor receptor
- 4.2. Fibroblast growth factor-mediated stromal-epithelial cross-talk in prostate tumors
- 4.3. Role of fibroblast growth factor in angiogenesis
- 4.3.1. Angiogenic synergism between fibroblast growth factor-2 and platelet derived growth factor-BB
- 4.3.2. Angiogenic synergism between fibroblast growth factor-2 and vascular endothelial growth factor
- 4.3.3. Clinical anti- angiogenesis target
- 5. Platelet-Derived Growth Factor and Receptor in Tumor Microenvironment
- 5.1. Platelet-derived growth factor and platelet-derived growth factor receptor
- 5.2. Role of platelet-derived growth factorin pancreatic tumor stroma
- 5.3. Role of platelet-derived growth factor in cervical carcinoma
- 5.4. Platelet-derived growth factorin tumor cell induced 'stromal resistance
- 6. Perspective
- 7. Acknowledgment
- 8. References
1. ABSTRACT
Tumor microenvironment plays a critical role in tumor initiation and progression. Components in the microenvironment can modulate the growth of tumor cells, their ability to progress and metastasize. A major venue of communication between tumor cells and their microenvironment is through polypeptide growth factors and receptors for these growth factors. This article discusses three major classes of growth-stimulatory polypeptide growth factors and receptors for these growth factors. It also discusses how deregulation of these growth factors or their receptors can drive malignant transformation and progression.