Autor: Bonavida, BenjaminNagaraju, Ganji Purnachandra
Wydawca: Elsevier
Dostępność: 3-6 tygodni
Cena: 778,05 zł
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ISBN13: |
9780128176610 |
Autor: |
Bonavida, BenjaminNagaraju, Ganji Purnachandra |
Oprawa: |
Hardback |
Rok Wydania: |
2019-03-08 |
Tematy: |
PSA |
Breaking Tolerance to Pancreatic Cancer Unresponsiveness to Chemotherapy edited by Dr. Nagaraju, PhD., DSc. focuses on overriding the resistance from chemotherapeutic drugs with a broader range of treatment options. It particularly focuses on stroma, tumor microenvironment, stem cells, stellate cells, transcription factors, growth factors, and important signaling pathways. This volume discusses topics such as pancreatic cancer biology, current therapeutic options, EMT, chemotherapy resistance mechanisms, and genetic manipulations and natural products to enhance the sensitivity of pancreatic cancer to chemotherapy. Additionally, it discusses small targeted molecules and pancreatic cancer trials, and nanotechnology-based drug delivery. Breaking Tolerance to Pancreatic Cancer Unresponsiveness to Chemotherapy is a valuable source for researchers and advanced students in cancer and oncology as well as clinicians and medical students who are interested in learning more about ways to break pancreatic cancer resistance to chemotherapy.
1. Overview of Pancreatic Cancer Biology 2. Chemoresistance in Pancreatic Cancer: Emphasis on Age and Gender 3. EMT Contributes to Chemoresistance in Pancreatic Cancer 4. Pancreatic Cancer Resistance to Gemcitabine 5. Pancreatic Cancer and Possible Therapeutic Options 6. Curcumin and Genistein Enhances the Sensitivity of Pancreatic Cancer to Chemotherapy 7. Terpenoids as Potential Targeted Therapeutics of Pancreatic Cancer: Current Advances and Future Directions 8. Small Molecules and Pancreatic Cancer Trials and Troubles 9. Targeting the Epigenome as a Therapeutic Strategy for Pancreatic Tumors - DNA and Histone Modifying Enzymes 10. Are Nanocarriers Effective for the Diagnosis and Treatment of Pancreatic Cancer? 11. Molecular Markers for Treatment Response and Toxicity of Gemcitabine
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