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Books > Medicine > Clinical & internal medicine > Diseases & disorders > Oncology > General
Completely dedicated to the biomedical applications of metal
nanoparticles, this book covers the different toxicity problems
found in healthcare situations and also provides comprehensive info
on the use of metal nanoparticles in treating various diseases.
Metal Nanoparticles in Pharma is the first edited volume to set up
the discussion for a clinical setting and to target a
pharmaceutical audience of academic and industry-based researchers.
This book provides an overview of the latest experimental work on
sex-based differences in lung function and inflammation. Readers
will learn how these differences relate to individual
predispositions for the development of lung disease in men and
women, and in different stages of their reproductive lives.
Further, the book focuses on diseases that predominantly affect
women or men, with an emphasis on the physiological mechanisms
underlying their pathobiology. In turn, these findings are
complemented by chapters on recent studies, which investigate how
circulating sex hormone levels impact the lung's innate immune
response to environmental agents and air pollution. The
pathogeneses of asthma and viral respiratory infection are also
major focus areas. As an outlook, the book also discusses current
and future research directions aimed at developing sex-specific
therapies for lung disease. To examine these anatomical and
physiological differences in the male and female respiratory
systems, the authors employ a broad range of methods from molecular
and clinical biology. Accordingly, the book will be a fascinating
read for physiologists and clinicians alike.
In the last decade, the literature on molecular mechanisms and
activated pathways in the different lymphoma categories increased
exponentially, which was followed by a more diffuse and successful
use of targeted therapies. In this book, expert authors revisit the
most relevant aspects of these therapies, with special emphasis on
molecular mechanisms and clinical effects of resistance. The
knowledge of the underlying mechanisms involved in tumor resistance
to target therapies is of paramount importance because they will
result in a better selection of patients with sensitive disease and
the establishment of suitable combinations of drugs that target
different molecules and could overcome the established resistance.
This book offers clear, accessible information on the causes of
cancer and the multiple ways people can reduce their risk for this
insidious disease. Like no other work, this much-needed volume
gathers the latest research and understanding about the causes of
cancer and methods of preventing the disease-and makes it all clear
and accessible to the general reader. Cancer Causes and
Controversies: Understanding Risk Reduction and Prevention
describes common risk factors associated with particular types of
cancer, including genetic predisposition, radiation and chemical
carcinogens, diet, hormonal factors, infection, and smoking. The
book then looks at the scientific evidence supporting the positive
role of healthy nutrition, exercise, and diet in lowering cancer
risk, as well as the dangers posed by a dysfunctional immune system
compromised by chronic infection, unhealthy lifestyles, stress, and
poor psychological health. Finally, the book provides an unbiased
assessment of a number of controversies surrounding cancer causes
and prevention, including screening and genetic testing, vitamin
supplementation, genetically modified foods, chemical food
additives, and cellular phones and deodorants as potential
cancer-causing agents. Primary source materials derived from
original scientific work including the National Resources for
Molecular Biology (National Center for Biotechnology Information
public database) and Cancer Research UK International scientific
manuscripts and reviews in the field of cancer research from peer
review journals Resources for more information on cancer (websites,
association, centers, books)
Tumor-Induced Immune Suppression - Prospects and Progress in
Mechanisms and Therapeutic Reversal presents a comprehensive
overview of large number of different mechanisms of immune
dysfunction in cancer and therapeutic approaches to their
correction. This includes the number of novel mechanisms that has
never before been discussed in previous monographs. The last
decades were characterized by substantial progress in the
understanding of the role of the immune system in tumor
progression. Researchers have learned how to manipulate the immune
system to generate tumor specific immune response, which raises
high expectations for immunotherapy to provide breakthroughs in
cancer treatment. It is increasingly clear that tumor-induced
abnormalities in the immune system not only hampers natural tumor
immune surveillance, but also limits the effect of cancer
immunotherapy. Therefore, it is critically important to understand
the mechanisms of tumor-induced immune suppression to make any
progress in the field and this monograph provides these important
insights.
This book covers core and emerging in vitro and in vivo protocols
used to study how various components of the tumor microenvironment
are established and subsequently interact with tumor cells to
facilitate carcinogenesis. In addition, the book examines research
topics including cellular and molecular biology approaches, in vivo
genetic approaches, various "omics"-based strategies, therapeutic
strategies to target the microenvironment, and, finally, advanced
techniques in the fields of tissue engineering and nanotechnology.
Written and validated in the laboratories of a number of trusted
collaborating authors for the highly successful Methods in
Molecular Biology series, chapters contain introductions to their
respective topics, lists of the necessary materials and reagents,
step-by-step, readily reproducible laboratory protocols, and tips
on troubleshooting and avoiding known pitfalls. Practical and
authoritative, The Tumor Microenvironment: Methods and Protocols
constitutes a compendium of techniques now available to a broad
audience, including basic and clinician scientists, systems
biologists, and biological engineers.
This volume aims to provide a range of methods and protocols for
studying tumor angiogenesis in vitro and in vivo to reflect
advances in the field. The chapters in this book cover topics such
as: morphological aspects of tumor angiogenesis, aortic ring assay
and its use for the study of tumor angiogenesis, ex vivo tissue
culture model for anti-angiogenic drug testing, transgenic
zebrafish, orthotopic models of ovarian cancer, and uncovering
metabolic effects of anti-angiogenic therapy in tumors by induced
metabolic bioluminescence imaging. Written in the highly successful
Methods in Molecular Biology series format, chapters include
introductions to their respective topics, lists of the necessary
materials and reagents, step-by-step, readily reproducible
laboratory protocols, and tips on troubleshooting and avoiding
known pitfalls. Cutting edge and thorough, Tumor Angiogenesis
Assays: Methods and Protocols is a valuable resource for anyone
interested in tumor angiogenesis assay research.
This book aims to provide scientists with tools and well-researched
protocols to enable their research and to facilitate further
progress in this common leukemia. Written in the highly successful
Methods in Molecular Biology series format, chapters include
introductions to their respective topics, lists of the necessary
materials and reagents, step-by-step, readily reproducible
laboratory protocols, and tips on troubleshooting and avoiding
known pitfalls. Authoritative and cutting-edge, Chronic Lymphocytic
Leukemia: Methods and Protocols aims to accelerate research on
chronic lymphocytic leukemia and further improvements in patient
outcomes.
This volume will outline how to recreate the tumor
microenvironment, to culture primary tumors without the need for
developmental priming factors, and to deliver targeted therapeutics
in a manner that recapitulates pharmacokinetics in vivo. Much of
what may be learned from this volume will aid in understanding many
aspects of the enhanced study of tumor cell biology in a
physiologic context, open new avenues for drug screening and
biomarker development, and accelerate the preclinical evaluation of
novel personalized medicine strategies for patients in real time.
This book is the first to focus specifically on cancer
nanotheranostics. Each of the chapters that make up this
comprehensive volume is authored by a researcher, clinician, or
regulatory agency member known for their expertise in this field.
Theranostics, the technology to simultaneously diagnose and treat a
disease, is a nascent field that is growing rapidly in this era of
personalized medicine. As the need for cost-effective disease
diagnosis grows, drug delivery systems that can act as
multifunctional carriers for imaging contrast and therapy agents
could provide unique breakthroughs in oncology. Nanotechnology has
enabled the development of smart theranostic platforms that can
concurrently diagnose disease, start primary treatment, monitor
response and initiate secondary treatments if required. In
oncology, chemotherapeutics have been routinely used. Some drugs
have proven effective but all carry risks of adverse side effects.
There is growing interest in using remotely triggered drug delivery
systems to limit cytotoxicity in the diseased area. This book
reviews the use of theranostic nanoparticles for cancer
applications over the past decade. First, it briefly discusses the
challenges and limitations of conventional cancer treatments, and
presents an overview of the use of nanotechnology in treating
cancer. These introductory chapters are followed by those exploring
cancer diagnosis and a myriad of delivery methods for
nanotherapeutics. The book also addresses multifunctional
platforms, treatment monitoring, and regulatory considerations. As
a whole, the book aims to briefly summarize the development and
clinical potential of various nanotheranostics for cancer
applications, and to delineate the challenges that must be overcome
for successful clinical development and implementation of such
cancer theranostics.
This book describes the most important techniques used for studying
cfDNA in the different samples; serum, plasma, urine. Chapters
detail methods on liquid biopsy for cancer disease, methods in
cancer, epigenetic modifications, fetal and pediatric diseases,
physical activity, and urinary cell free DNA. Written in the highly
successful Methods in Molecular Biology series format, chapters
include introductions to their respective topics, lists of the
necessary materials and reagents, step-by-step, readily
reproducible laboratory protocols, and tips on troubleshooting and
avoiding known pitfalls. Authoritative and cutting-edge, Cell-Free
DNA as Diagnostic Markers: Methods and Protocols aims to ensure
successful results in the further study of this vital field.
This book presents a systematic overview of the most relevant
nanomaterials and their respective intrinsic properties that have
been highly explored by the scientific community and pharmaceutical
companies in several different modalities for cancer therapy and
bioimaging. The chapters explore the synergistic effects provided
by the different nanostructured materials and highlight the main in
vitro and in vivo therapeutic achievements on cancer. This work
also provides relevant discussion about the recent progresses and
future challenges that nanotechnology faces on the conception of
more efficient nanoformulations against primary tumors, circulating
cancer cells and metastases.
This volume gives a state-of-the-art overview on macrophage
functions in various invertebrate and vertebrate systems and
diseases. It also covers various aspects of macrophage development
and formation, behavior and response to nano- and biomaterials, the
latter of which have become very important components of modern
medicine. Macrophages are evolutionarily conserved phagocytotic
cells. In recent years macrophages have emerged as one of the most
versatile cells of immune system, which, depending on the milieu
and circumstance, participate in development or inhibition of
cancer, regeneration, wound healing, inflammation, organ rejection
and interaction between mother and a fetus. This book will be of
particular interest to researchers working in immunology, cancer
research, developmental biology, or related fields.
This astute volume brings together the latest expert research on
adamantinomatous craniopharyngiomas (ACPs). ACPs are histologically
benign but clinically aggressive tumors exhibiting a high
propensity for local invasion into the hypothalamus, optic and
vascular structures. These tumors, as well as the current
treatments, may result in pan-hypopituitarism, diabetes insipidus,
morbid obesity followed by type II diabetes mellitus, blindness, as
well as serious behavioral and psychosocial impairments. Exploring
in detail advances in both the understanding of tumor biology as
well as clinical advances in patient management are explored in
detail, this book will also look towards potential new treatment
approaches. Basic Research and Clinical Aspects of Adamantinomatous
Craniopharyngioma is the first book compiling all current research
on ACPs. Mouse and human studies have unequivocally demonstrated
that mutations in CTNNB1 encoding -catenin underlie the etiology of
the majority, if not all ACP tumors. Genetic studies in mice have
shown that ACPs are tumors of the pituitary gland and not of the
hypothalamus as previously thought, and are derived from Rathke's
pouch precursors. In addition, a role for tissue-specific adult
pituitary stem cells has been revealed as causative of ACP.
Together, these studies have provided novel insights into the
molecular and cellular etiology as well as the pathogenesis of
human ACP. Finally, this volume covers new treatment approaches
that have been shown to be effective both in reducing ACP burden as
well as reducing the morbidity associated with therapy.
This book is intended to serve as an authoritative reference source
for a broad audience involved in the research, teaching, learning,
and practice of nanotechnology in immunotherapy. The combination of
nanotechnology and immunotherapy is recognized as a promising
treatment modality. In particular, the use of nanoparticles in
immunotherapy has attracted increased attention for their unique
efficacy and specificity in cancer treatment. A wide variety of
nanoparticles, such as polymeric and liposomal nanosystems, carbon
nanotubes, and gold nanoparticles have provided important
nanoplatforms for immunotherapeutic approaches. They have been
shown to improve delivery and efficacy of immunotherapeutic agents
such as vaccines or adjuvants. Nanoparticle-mediated thermal
therapy has demonstrated the effectiveness for precise tumor cell
ablation, radio-sensitization of hypoxic regions, enhancement of
drug delivery, activation of thermosensitive agents, and
enhancement of the immune system. Plasmonic nanoparticles are a
special type of metallic nanoparticles that has received great
interest due to their enhanced optical and electromagnetic
properties and their superior capacity to convert photon energy
into heat for selective photothermal therapy at the nanoscale
level. Nanoparticle sizes can also be controlled such that they
accumulate preferentially in tumors due to the enhanced
permeability and retention effect of tumor vasculature. Various
nanosystems such as gold nanoparticles have also been shown to
stimulate the immune system. Immunotherapies could thus
synergistically benefit from the combination with targeted
nanoparticle-mediated photothermal therapies, especially when
hyperthermia around immune-checkpoint inhibitors in the tumor bed
is combined with precise thermal ablation of cancer cells. Of great
importance is the possibility that such an approach can induce
long-term immunological memory that can provide protection against
tumor recurrence long after treatment of the initial tumors, like
an 'anticancer vaccine'. Nanoparticle-mediated immunotherapy could
lead to an entirely new treatment paradigm that challenges
traditional surgical resection approaches for many cancers and
metastases.
The book conveys a comprehensive knowledge of long and short ncRNAs
in cancer regulation and their potentials as diagnostic biomarkers
and therapeutic targets. Topics covered include the molecular
mechanisms of various classes of ncRNAs (with emphasis on long
non-coding RNAs and microRNAs) in cancer, the functional roles of
ncRNAs in regulating different cancer hallmarks (including
proliferation, apoptosis, stem-cell properties,
epithelial-mesenchymal transition, metabolism, angiogenesis,
tumor-host interactions and therapeutic resistance), the role of
ncRNAs in regulating cancer signaling circuitry programs
(highlighting their involvement in c-myc, p53 and NFkB signaling),
a systemic summary of clinical and preclinical studies that
evaluate the potential of ncRNA signatures for cancer diagnosis and
prognosis and strategies to delivery short ncRNAs as therapeutic
molecules for cancer treatment. This book may serve as a
comprehensive resource for researchers, graduate students and
oncologists in ncRNA and cancer research and help drug development
by identifying ncRNA targets.
This book presents a comprehensive discussion on the heterogeneity
existing between different types of stem cells within the same
tissue, for several types of cancers, e.g. glioblastoma stem cells.
Recent developments have revealed completely different roles of
distinct stem cells within the same organ. Thus, Stem Cells
Heterogeneity in Cancer provides a timely update us on the current
information on stem cells heterogeneity in various tissues. It also
provides a solid foundation of the history of stem cells from
specific tissues and the current applications of this knowledge in
regenerative medicine. When taken as a whole, alongside its
companion volumes Stem Cells Heterogeneity - Novel Concepts, and
Stem Cells Heterogeneity in Different Organs, these three books
present a comprehensive reference on stem cell heterogeneity in
various tissues and current and future applications for
regenerative medicine. It is essential reading for advanced cell
biology students as well as researchers in stem cells and
clinicians.
Gynecologic malignancies, especially endometrial and ovarian
cancers are among the most important and most severely affected by
obesity. This volume of Energy Balance and Cancer, written by the
world's leading experts in this field, is arranged to provide a
transdisciplinary assessment of the pertinent issues, results of
relevant research on mechanisms, and control, strategies for
dealing with affected patients and improving outcomes and future
research needs. The volume comprehensively covers the epidemiology
linking obesity to endometrial and ovarian cancer as well as the
public awareness of this critical problem. Subsequent chapters
explain biologic aspects of linkages between energy balance and
gynecologic malignancies. The volume further outlines strategies to
disrupt the linkage between obesity and gynecologic malignancies
and concludes with a series of chapters focused on management
strategies for obese patients with gynecologic malignancies. This
volume provides a valuable resource for all physicians, scientists
and other transdisciplinary investigators and practitioners
interested and involved in energy balance and cancer. It should be
a particularly useful guide to optimize outcomes for all
practitioners dealing with patients with gynecologic malignancies
challenged by energy balance issues. Moreover, it should serve as a
useful guide to students and investigators interested in conducting
further research on defining and disrupting the important linkage
between energy balance and gynecologic malignancies.
1 Dietary Fat and Breast Cancer: Controversy and Biological
Plausibility.- 2 Dietary Fat Intake Reduction for Patients with
Resected Breast Cancer.- 3 Dietary Fat Reduction as a Hypothesis
for the Prevention of Postmenopausal Breast Cancer, and a
Discussion of Hypothesis Testing Research Strategies.- 4 Hormone
Studies and the Diet and Breast Cancer Connection.- 5 Dietary Fat
Effects on Animal Models of Breast Cancer.- 6 Effect of Conjugated
Linoleic Acid on Carcinogenesis.- 7 A Possible Mechanism by Which
Dietary Fat Can Alter Tumorigenesis: Lipid Modulation of Macrophage
function.- 8 Dietary Fatty Acids and Human Breast Cancer Cell
Growth, Invasion, and Metastasis.- 9 Meta-Analysis of Animal
Experiments: Elucidating Relationships Between Dietary Fat and
Mammary Tumor Development in Rodents.- 10 Vitamin A, Retinoids and
Breast Cancer.- 11 Vitamin D Adequacy: A Possible Relationship to
Breast Cancer.- 12 Vitamin D and Breast Cancer.- 13 Some Aspects of
Vitamin E Related to Humans and Breast Cancer Prevention.- Poster
Abstract.- Contributors.
This volume will describe recent progress and future directions in
radiation oncology and biology research, focusing on strategies
designed to improve disease control and reduce the risk of
long-term adverse effects on patients. As more and more patients
are becoming long-term survivors, this strategy will become
increasingly important--in radiation oncology and throughout the
field of oncology.
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