Dr. Andrew Freywald, obtained his PhD in molecular and cell biology at the Weizmann Institute of Science, Israel, and completed his post-doctorate training in molecular immunology and cancer research at the Hospital for Sick Children, Toronto, Canada. His current research interests include cancer cell biology and tumor biology. He also serves as a scientific advisor for the biotech industry. The work of his research team at the College of Medicine, University of Saskatchewan focuses on investigating and targeting molecular mechanisms that determine tumor aggressiveness, and treatment resistance. His research program has been supported by several granting agencies, including CIHR, CCSRI, SHRF CRS, CFI, SCA, PCC, CBCF and TFRI, and also by the Be Like Bruce organization and the College of Medicine, University of Saskatchewan. Dr. Franco J. Vizeacoumar, obtained his PhD in cell biology at the University of Alberta, Canada, and did his post-doctorate at the University of Toronto, Canada. His lab is working on developing genotype-directed cancer therapies for solid tumors by applying basic biological concepts called synthetic lethality and synthetic dosage lethality. The long term goal of his research group is to build a unified human genetic network that will capture genetic dependencies of cancer cells and define key therapeutic targets. The work in the Vizeacoumar lab has been supported by multiple granting agencies, such as CIHR, SCA, CRS, SHRF, CFI, TFRI, PCC, and also by the Be Like Bruce organization and the College of Medicine at the University of Saskatchewan.

• 1. Introductory Chapter2. Tumor Metabolic Reprogramming in Therapeutic Resistance3. Development of novel antiandrogens to overcome castrate resistant prostate cancer4. Microenvironmental regulation of cancer response to therapy and therapy resistance5. Revisiting immunogenic cell death to overcome treatment resistance in cancer immunotherapy6. Preventing Phenotypic Plasticity in Cancer to Mitigate Therapy Resistance7. Overcoming drug resistance in cancer with targeted radionuclide therapy8. The PI3K pathway and chemotherapy resistance9. Targeting leukemia stem cells in T-cell acute lymphoblastic leukemia10. Escape from apoptosis: Anastasis as a potential mechanism of cancer drug resistance11. From genetic data and structures to drug development: new approaches to targeting Eph receptors12. Overcoming Therapeutic Resistance in Glioblastoma: a major clinical challenge

Dr. Andrew Freywald, obtained his PhD in molecular and cell biology at the Weizmann Institute of Science, Israel, and completed his post-doctorate training in molecular immunology and cancer research at the Hospital for Sick Children, Toronto, Canada. His current research interests include cancer cell biology and tumor biology. He also serves as a scientific advisor for the biotech industry. The work of his research team at the College of Medicine, University of Saskatchewan focuses on investigating and targeting molecular mechanisms that determine tumor aggressiveness, and treatment resistance. His research program has been supported by several granting agencies, including CIHR, CCSRI, SHRF CRS, CFI, SCA, PCC, CBCF and TFRI, and also by the Be Like Bruce organization and the College of Medicine, University of Saskatchewan. Dr. Franco J. Vizeacoumar, obtained his PhD in cell biology at the University of Alberta, Canada, and did his post-doctorate at the University of Toronto, Canada. His lab is working on developing genotype-directed cancer therapies for solid tumors by applying basic biological concepts called synthetic lethality and synthetic dosage lethality. The long term goal of his research group is to build a unified human genetic network that will capture genetic dependencies of cancer cells and define key therapeutic targets. The work in the Vizeacoumar lab has been supported by multiple granting agencies, such as CIHR, SCA, CRS, SHRF, CFI, TFRI, PCC, and also by the Be Like Bruce organization and the College of Medicine at the University of Saskatchewan.

• 1. Introductory Chapter2. Tumor Metabolic Reprogramming in Therapeutic Resistance3. Development of novel antiandrogens to overcome castrate resistant prostate cancer4. Microenvironmental regulation of cancer response to therapy and therapy resistance5. Revisiting immunogenic cell death to overcome treatment resistance in cancer immunotherapy6. Preventing Phenotypic Plasticity in Cancer to Mitigate Therapy Resistance7. Overcoming drug resistance in cancer with targeted radionuclide therapy8. The PI3K pathway and chemotherapy resistance9. Targeting leukemia stem cells in T-cell acute lymphoblastic leukemia10. Escape from apoptosis: Anastasis as a potential mechanism of cancer drug resistance11. From genetic data and structures to drug development: new approaches to targeting Eph receptors12. Overcoming Therapeutic Resistance in Glioblastoma: a major clinical challenge

Dr. Andrew Freywald, obtained his PhD in molecular and cell biology at the Weizmann Institute of Science, Israel, and completed his post-doctorate training in molecular immunology and cancer research at the Hospital for Sick Children, Toronto, Canada. His current research interests include cancer cell biology and tumor biology. He also serves as a scientific advisor for the biotech industry. The work of his research team at the College of Medicine, University of Saskatchewan focuses on investigating and targeting molecular mechanisms that determine tumor aggressiveness, and treatment resistance. His research program has been supported by several granting agencies, including CIHR, CCSRI, SHRF CRS, CFI, SCA, PCC, CBCF and TFRI, and also by the Be Like Bruce organization and the College of Medicine, University of Saskatchewan. Dr. Franco J. Vizeacoumar, obtained his PhD in cell biology at the University of Alberta, Canada, and did his post-doctorate at the University of Toronto, Canada. His lab is working on developing genotype-directed cancer therapies for solid tumors by applying basic biological concepts called synthetic lethality and synthetic dosage lethality. The long term goal of his research group is to build a unified human genetic network that will capture genetic dependencies of cancer cells and define key therapeutic targets. The work in the Vizeacoumar lab has been supported by multiple granting agencies, such as CIHR, SCA, CRS, SHRF, CFI, TFRI, PCC, and also by the Be Like Bruce organization and the College of Medicine at the University of Saskatchewan.

• 1. Introductory Chapter2. Tumor Metabolic Reprogramming in Therapeutic Resistance3. Development of novel antiandrogens to overcome castrate resistant prostate cancer4. Microenvironmental regulation of cancer response to therapy and therapy resistance5. Revisiting immunogenic cell death to overcome treatment resistance in cancer immunotherapy6. Preventing Phenotypic Plasticity in Cancer to Mitigate Therapy Resistance7. Overcoming drug resistance in cancer with targeted radionuclide therapy8. The PI3K pathway and chemotherapy resistance9. Targeting leukemia stem cells in T-cell acute lymphoblastic leukemia10. Escape from apoptosis: Anastasis as a potential mechanism of cancer drug resistance11. From genetic data and structures to drug development: new approaches to targeting Eph receptors12. Overcoming Therapeutic Resistance in Glioblastoma: a major clinical challenge