Analysis of cellular resistance mechanisms to viral oncolysis

Vectors based on adenoviruses have been designed as targeted anti-cancer therapeutics that showed promising results in pre-clinical applications. Particularly, efforts have focused on the development of oncolytic vectors that can eliminate cancer cells and replicate in a tumor-selective fashion to amplify the input dose. In clinical trials, these oncolytic adenoviruses have generally been proved safe in patients, but have fallen short of their expected therapeutic value as monotherapies. A number of obstacles that hamper the efficacy of adenoviral vectors have been identified. These include several soluble and cellular blood components, the lack of viral receptors, and the extracellular matrix sequestered by tumor stroma. However, the apparent inability of adenoviruses to spread throughout solid tumors could not be fully explained yet. The work in this book sheds light on obstacles that previously had not been taken into account. It was identified that the epithelial phenotype of ovarian cancer cells represents a barrier for adenovirus infection and virus-mediated oncolysis. Furthermore, major discrepancies between phenotypes of tumors in situ and cultured cells were discovered.

Autorentext

The author was born in 1976 in Berlin, Germany. He received his biology diploma from the Freie Universität Berlin in 2004 and thereafter joined the University of Washington (Seattle, USA) for his external PhD studies in molecular biology. His thesis was supervised by the Humboldt-Universität zu Berlin, from where he graduated in January 2010.