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Topics in Anti-Cancer Research 7 PDF

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Patents eBook Series “Topics in Anti-Cancer Research” (Volume 7) Edited by Atta-ur-Rahman, FRS Honorary Life Fellow, Kings College,University of Cambridge,Cambridge,UK & Khurshid Zaman Bentham Science Publishers, USA Topics in Anti-Cancer Research Volume # 7 Editors: Atta-ur-Rahman, FRS and Khurshid Zaman ISSN (Print): 2468-5860 ISSN (Online): 2213-3585 ISBN (Online): 978-1-68108-627-9 ISBN (Print): 978-1-68108-628-6 ©2018, Bentham eBooks imprint. Published by Bentham Science Publishers – Sharjah, UAE. All Rights Reserved. BENTHAM SCIENCE PUBLISHERS LTD. End User License Agreement (for non-institutional, personal use) This is an agreement between you and Bentham Science Publishers Ltd. Please read this License Agreement carefully before using the ebook/echapter/ejournal (“Work”). Your use of the Work constitutes your agreement to the terms and conditions set forth in this License Agreement. If you do not agree to these terms and conditions then you should not use the Work. 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Any dispute or claim arising out of or in connection with this License Agreement or the Work (including non-contractual disputes or claims) will be governed by and construed in accordance with the laws of the U.A.E. as applied in the Emirate of Dubai. Each party agrees that the courts of the Emirate of Dubai shall have exclusive jurisdiction to settle any dispute or claim arising out of or in connection with this License Agreement or the Work (including non-contractual disputes or claims). 2. Your rights under this License Agreement will automatically terminate without notice and without the need for a court order if at any point you breach any terms of this License Agreement. In no event will any delay or failure by Bentham Science Publishers in enforcing your compliance with this License Agreement constitute a waiver of any of its rights. 3. You acknowledge that you have read this License Agreement, and agree to be bound by its terms and conditions. To the extent that any other terms and conditions presented on any website of Bentham Science Publishers conflict with, or are inconsistent with, the terms and conditions set out in this License Agreement, you acknowledge that the terms and conditions set out in this License Agreement shall prevail. Bentham Science Publishers Ltd. Executive Suite Y - 2 PO Box 7917, Saif Zone Sharjah, U.A.E. Email: [email protected] CONTENTS PREFACE ................................................................................................................................................ i INTRODUCTION ................................................................................................................................... ii LIST OF CONTRIBUTORS .................................................................................................................. iii CHAPTER 1 THE ROLE OF ncRNAs IN HUMAN CANCER AND ITS RELATED PATENTS 1 María I. Navarro-Mendoza, Carlos Pérez-Arques, Laura Murcia, Alfonso F. López-Martínez and Francisco E. Nicolás 1. INTRODUCTION ...................................................................................................................... 1 2. SMALL ncRNAs: miRNAs, piRNAs, tiRNAs, snoRNAs AND paRNAs ............................... 4 2.1. miRNAs ........................................................................................................................... 4 2.2. piRNAs ............................................................................................................................ 6 2.3. tiRNAs ............................................................................................................................. 6 2.4. snoRNAs .......................................................................................................................... 7 2.5. Small Promoter Associated RNAs ................................................................................... 8 2.6. Other Small ncRNAs ....................................................................................................... 9 3. LONG ncRNAs: lincRNAs, T-UCRs, ceRNAs AND OTHER lncRNAs ............................... 11 3.1. lincRNAs ........................................................................................................................ 11 3.2. T-UCRs ............................................................................................................................ 12 3.3. ceRNAs ........................................................................................................................... 13 3.4. Other lncRNAs ................................................................................................................. 14 CURRENT & FUTURE DEVELOPMENTS .............................................................................. 15 CONSENT FOR PUBLICATION ................................................................................................ 16 CONFLICT OF INTEREST ......................................................................................................... 16 ACKNOWLEDGEMENTS ........................................................................................................... 16 DISCLOSURE ................................................................................................................................ 16 REFERENCES ............................................................................................................................... 17 CHAPTER 2 TAXOL TO NANOTAXOL: A JOURNEY TOWARDS ENHANCED DRUG DELIVERY .............................................................................................................................................. 25 Tanvi Kaku, Aiswarya Dash and Biswa P. Chatterji 1. INTRODUCTION ...................................................................................................................... 26 1.1. Methods for Preparation of Paclitaxel Nanoparticles ...................................................... 29 1.1.1. CN1463969A ....................................................................................................... 29 1.1.2. CN101829061A ................................................................................................... 30 1.2. Human Serum Albumin (HSA) Associated and Other Protein Associated and Functionalized Taxol® or Paclitaxel Nanoparticles as Drug Delivery Agents ....................... 30 1.2.1. US6506405B1 ..................................................................................................... 30 1.2.2. US8268348B2 and US20100112077A1 .............................................................. 32 1.2.3. WO1994018954A1 .............................................................................................. 32 1.2.4. US20040092577A1 ............................................................................................. 32 1.2.5. US20090004118 .................................................................................................. 33 1.2.6. US20090226393 .................................................................................................. 33 1.2.7. US20100015051 .................................................................................................. 33 1.2.8. US20100303723 .................................................................................................. 34 1.2.9. WO2007034479 ................................................................................................... 34 1.3. Micelles, Emulsions and Liposomes as Drug Delivery Carriers for Paclitaxel ............... 34 1.3.1. US20150366806 .................................................................................................. 34 1.3.2. WO2009070761 ................................................................................................... 34 1.3.3. EP2494956 and EP2494957 ............................................................................... 35 1.3.4. WO1994007484 ................................................................................................... 35 1.3.5. WO1996002247 ................................................................................................... 35 1.3.6. CN102772368A ................................................................................................... 36 1.3.7. US5424073 .......................................................................................................... 36 1.3.8. KR101612194 ...................................................................................................... 36 1.3.9. US8663599B1 ..................................................................................................... 37 1.4. Carbon Nanoparticles as Drug Delivery Agents for Cancer Chemotherapy ................... 37 1.4.1. EP3063091 .......................................................................................................... 37 1.4.2. US20090087493 .................................................................................................. 37 1.4.3. KR20180016231 .................................................................................................. 38 1.4.4. CN104998261 ..................................................................................................... 38 1.4.5. WO2014015334 ................................................................................................... 38 1.5. Nanodevices for Paclitaxel Delivery to Cancer Cells ...................................................... 39 1.5.1. US20100215724 .................................................................................................. 39 1.5.2. US20100303716 .................................................................................................. 39 DISCUSSION .................................................................................................................................. 39 CURRENT & FUTURE DEVELOPMENTS .............................................................................. 40 CONSENT FOR PUBLICATION ................................................................................................ 41 CONFLICT OF INTEREST ......................................................................................................... 41 ACKNOWLEDGEMENTS ........................................................................................................... 41 REFERENCES ............................................................................................................................... 41 CHAPTER 3 ADVANCED THERAPY IN CANCER: STIMULI-RESPONSIVE NANOCARRIERS FOR ON-DEMAND DRUG DELIVERY ............................................................ 48 Azadeh Haeri, Fatemeh Mehryab and Hamid R. Moghimi 1. INTRODUCTION ...................................................................................................................... 48 2. STIMULI-RESPONSIVE NANOCARRIERS ........................................................................ 51 3. EXTERNAL STIMULI-RESPONSIVE DRUG DELIVERY ................................................ 51 3.1. Temperature-Responsive Nanocarriers ............................................................................ 51 3.2. Magnetic Field-Responsive Nanocarriers ........................................................................ 56 3.3. Photo-Responsive Nanocarriers ....................................................................................... 61 3.4. Ultrasound-Responsive Nanocarriers .............................................................................. 64 4. INTERNAL STIMULI-RESPONSIVE DRUG DELIVERY ................................................. 68 4.1. pH-Responsive Nanocarriers ........................................................................................... 68 4.2. Enzyme-Responsive Nanocarriers ................................................................................... 74 4.3. Redox-Responsive Nanocarriers ...................................................................................... 78 5. OTHER STIMULI-RESPONSIVE NANOCARRIERS ......................................................... 82 CONCLUSION ............................................................................................................................... 82 CURRENT & FUTURE DEVELOPMENTS ............................................................................. 82 CONSENT FOR PUBLICATION ............................................................................................... 83 CONFLICT OF INTEREST ......................................................................................................... 83 ACKNOWLEDGEMENTS .......................................................................................................... 83 REFERENCES ............................................................................................................................... 83 CHAPTER 4 THE REGULATION AND THE FUNCTION OF AUTOPHAGY IN THE DEVELOPMENT AND BEHAVIOR OF ESOPHAGEAL CANCERS ............................................ 96 Erdem Ayik and Gulsum O. Elpek 1. INTRODUCTION ...................................................................................................................... 97 2. GENERAL ASPECTS OF AUTOPHAGY .............................................................................. 97 3. AUTOPHAGY IN CANCER ..................................................................................................... 101 3.1. AP in Malignant Transformation ..................................................................................... 101 3.2. AP in Cancer Behavior and Treatment ............................................................................ 102 4. AUTOPHAGY IN ESOPHAGEAL CANCER ........................................................................ 104 4.1. Autophagy in the Development of EAC .......................................................................... 105 4.2. Autophagy in the Development of ESCC ........................................................................ 106 4.3. Autophagy in EAC Behavior and Treatment ................................................................... 108 4.3.1. AP-Related Findings on Tumor Behavior and Progression in Patients with EAC 108 4.3.2. In Vitro Investigation of AP in EAC .................................................................... 110 4.4. Autophagy in ESCC Behavior and Treatment ................................................................. 112 4.4.1. AP-Related Findings in Tumor Behavior and Progression in Patients with ESCC ............................................................................................................................. 112 4.4.2. In Vitro Investigation of AP in ESCC ................................................................. 116 CONCLUSION ............................................................................................................................... 126 CURRENT & FUTURE DEVELOPMENTS .............................................................................. 126 CONSENT FOR PUBLICATION ................................................................................................ 127 CONFLICT OF INTEREST ......................................................................................................... 127 ACKNOWLEDGEMENTS ........................................................................................................... 127 LIST OF ABBREVIATIONS ........................................................................................................ 127 REFERENCES ............................................................................................................................... 128 CHAPTER 5 RECENT PATENTS ON SMART NANO-FORMULATIONS FOR CANCER THERAPY ................................................................................................................................................ 145 Shaheen Sultana, Mohammad Yusuf and Maria Khan 1. INTRODUCTION ...................................................................................................................... 146 1.1. Polymer-Based Nano-Formulations ................................................................................. 146 1.1.1. Polymeric Nanoparticles ..................................................................................... 147 1.1.2. Hydrogels ............................................................................................................ 151 1.1.3. Dendrimers .......................................................................................................... 152 1.1.4. Micelles ............................................................................................................... 152 1.2. Virus-Based Nanoparticles .............................................................................................. 154 1.3. Carbon Nanotubes ............................................................................................................ 154 1.4. Lipid-Based Nano-Formulation ....................................................................................... 157 1.4.1. Liposomes ............................................................................................................ 157 1.4.2. Solid Lipid Nanoparticles ................................................................................... 158 1.5. Metal-Based Nanoparticles .............................................................................................. 159 1.5.1. Gold Nanoparticles (AuNPs) .............................................................................. 160 1.5.2. Magnetic Nanoparticles (MNPs) ........................................................................ 161 CONCLUSION ............................................................................................................................... 165 CURRENT & FUTURE DEVELOPMENTS .............................................................................. 165 CONSENT FOR PUBLICATION ................................................................................................ 165 CONFLICT OF INTEREST ......................................................................................................... 165 ACKNOWLEDGEMENTS ........................................................................................................... 165 REFERENCES ............................................................................................................................... 165 CHAPTER 6 POTENTIAL INFLAMMATORY MECHANISMS UNDERLYING CHEMOTHERAPY-INDUCED PERIPHERAL NEUROPATHY AND SKELETAL MUSCLE EFFECTS ................................................................................................................................................. 173 Claire E. Feather, John B. Kwok, Gila Moalem-Taylor and Patsie Polly 1. INTRODUCTION ...................................................................................................................... 174 1.1. Chemotherapy, Neuropathic Pain and Skeletal Muscle Effects ...................................... 174 1.2. Clinical Insights ............................................................................................................... 175 2. AN OVERVIEW OF CHEMOTHERAPY-INDUCED NEUROMUSCULAR EFFECTS 176 2.1. Chemotherapy-Induced Peripheral Neuropathy (CIPN) .................................................. 176 2.1.1. Animal Models .................................................................................................... 177 2.2. Effects of Chemotherapy on Muscle ................................................................................ 178 2.2.1. Animal Models .................................................................................................... 179 3. CHEMOTHERAPY AND INFLAMMATION ....................................................................... 180 3.1. Cytokines ......................................................................................................................... 180 3.2. Reactive Oxygen Species ................................................................................................. 182 4. INFLAMMATION-ASSOCIATED MOLECULAR PATHWAYS OF INTEREST ........... 183 4.1. Upstream Inflammatory Signaling Pathways .................................................................. 183 4.2. Endoplasmic Reticulum Stress ........................................................................................ 184 4.3. Paclitaxel-Specific Molecular Alterations ....................................................................... 184 5. GENETIC SUSCEPTIBILITY TO CHEMOTHERAPY-INDUCED NEUROMUSCULAR EFFECTS .................................................................................................. 185 6. CANCER-INDUCED AND CHEMOTHERAPY-INDUCED EFFECTS ............................ 186 7. RECENT DEVELOPMENTS IN THE TARGETING OF CHEMOTHERAPY- INDUCED NEUROMUSCULAR EFFECTS .............................................................................. 187 CONCLUSION ............................................................................................................................... 191 CURRENT & FUTURE DEVELOPMENTS .............................................................................. 191 CONFLICT OF INTEREST ......................................................................................................... 192 ACKNOWLEDGEMENTS ........................................................................................................... 192 REFERENCES ............................................................................................................................... 192 CHAPTER 7 RECENT ADVANCES IN NUTRIGENOMICS: PATENT APPLICATIONS ...... 202 Elvan Y. Akyuz, Ozlem Aytekin, Banu Bayram and Yusuf Tutar 1. INTRODUCTION ...................................................................................................................... 202 1.1. Nutrigenomics and its Relation to Cancer ....................................................................... 204 1.2. Nutrition, Epigenetics, and Genome Stability ................................................................. 205 1.3. Diet and Cancer Prevention ............................................................................................. 206 1.4. Composition and Method to Optimize and Customize Nutritional Supplement Formulations by Measuring Genetic and Metabolomic Contributing Factors to Disease Diagnosis, Stratification, Prognosis, Metabolism, and Therapeutic Outcomes - US20060062859 ..................................................................................................................... 207 1.5. Nutraceutical Compositions and Methods with Biologically Active Ingredients - US20080317734 ..................................................................................................................... 208 1.6. Diagnostic System for Selecting Nutrition and Pharmacological Products for Animals - US7873482 ............................................................................................................................. 209 1.7. System and Method for Evaluating and Providing Nutrigenomic Data, Information and Advice - US7877273 ............................................................................................................... 209 1.8. Multi-Stage Nutrigenomic Diagnostic Food Sensitivity Testing in Animals - US8450072 ............................................................................................................................. 210 1.9. Predictive Markers for Cancer and Metabolic Syndrome - US2013045535 ................... 212 1.10. Novel Compositions from Nigella Sativa - US20150004266 ........................................ 214 1.11. Method of Dietary Treatment for Genetic and Epigenetic Diseases and Disorders - US20170056357 ..................................................................................................................... 216 1.12. Bioenergetics Profiling of Circulating Blood Cells and Systems, Devices, and Methods Relating Thereto - US2015024795 .......................................................................... 217 CONCLUSION ............................................................................................................................... 218 CURRENT & FUTURE DEVELOPMENTS .............................................................................. 218 CONSENT FOR PUBLICATION ................................................................................................ 219 CONFLICT OF INTEREST ......................................................................................................... 219 ACKNOWLEDGEMENTS ........................................................................................................... 219 REFERENCES ............................................................................................................................... 219 AUTHOR INDEX .................................................................................................................................... 221 SUBJECT INDEX ................................................................................................................................... 2(cid:21)(cid:21) i PREFACE Topics in Anti-Cancer Research covers important advances in both experimental (pre- clinical) and clinical cancer research in drug development. The book series offers readers an insight into current and future therapeutic approaches for the prevention of different types of cancers, synthesis of new anti-cancer agents, new patented compounds, targets and agents for cancer therapy as well as recent molecular and gene therapy research. The topics covered in the seventh volume of this series include the role of inflammation in chemotherapy-induced neuromuscular effects, recent advances in nutrigenomics and relevant anti-cancer patents, nanocarriers for on-demand anti-cancer drug release, biochemical mechanisms that control autophagy for treating esophageal cancer, nano-formulations for cancer therapy and nanotaxol. The comprehensive range of themes covered will be beneficial to clinicians, cancer pro- fessionals, immunologists, and R&D experts looking for new anti-cancer targets and patents for the treatment of neoplasms, as well as varied approaches for cancer therapy. We are obliged to the authors for their contributions and to the reviewers for their com- prehensive comments for shaping up the chapters and improving their quality. We extend our thanks to Mr. Mahmood Alam, Mrs. Rafia Rehan and other colleagues for their cooperation in the finalization of this volume. Atta-ur-Rahman, FRS International Center for Chemical and Biological Sciences University of Karachi Karachi 75270 Pakistan Khurshid Zaman Honorary Editor Bentham Science Publishers

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