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Principles of Cancer Genetics

Autor Fred Bunz
en Limba Engleză Paperback – 7 apr 2018
This is the second edition of a widely used textbook that consolidates the basic concepts of the cancer gene theory and provides a framework for understanding the genetic basis of cancer. Particular attention is devoted to the origins of the mutations that cause cancer, and the application of evolutionary theory to explain how the cell clones that harbor cancer genes tend to expand. Focused on the altered genes and pathways that cause the growth of the most common tumors, Principles of Cancer Genetics is aimed at advanced undergraduates who have completed introductory coursework in genetics, biology and biochemistry, medical students and medical house staff. For students with a general interest in cancer, this book provides a highly accessible and readable overview. For more advanced students contemplating future study in the field of oncology and cancer research, this concise book will be useful as a primer.
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Specificații

ISBN-13: 9789402413571
ISBN-10: 940241357X
Pagini: 343
Ilustrații: XII, 343 p. 138 illus., 29 illus. in color.
Dimensiuni: 155 x 235 x 23 mm
Greutate: 0 kg
Ediția:Softcover reprint of the original 2nd ed. 2016
Editura: SPRINGER NETHERLANDS
Colecția Springer
Locul publicării:Dordrecht, Netherlands

Cuprins

 
Preface
Chapter 1: The Genetic Basis of Cancer
The cancer gene theory
Cancers are invasive tumors
Cancer is a unique type of genetic disease
What are cancer genes and how are they acquired?
Mutations alter the human genome
Genes and mutations
Single nucleotide substitutions Gene silencing is marked by cytosine methylation: epigenetics
Environmental mutagens, mutations and cancer
Inflammation promotes the propagation of cancer genes
Stem cells, Darwinian selection and the clonal evolution of cancers
Selective pressure and adaptation:  hypoxia and altered metabolism
Multiple somatic mutations punctuate clonal evolution
Tumor growth leads to cellular heterogeneity Tumors are distinguished by their spectrum of driver gene mutations and passenger gene mutations
Colorectal cancer: a model for understanding the process of tumorigenesis
Do cancer cells divide more rapidly than normal cells?
Germline cancer genes allow neoplasia to bypass steps in clonal evolution
Cancer syndromes reveal rate-limiting steps in tumorigenesis
The etiolog
ic triad: heredity, the environment, and stem cell division Understanding cancer genetics
 
Chapter 2:  Oncogenes
What is an oncogene?
The discovery of transmissible cancer genes
Viral oncogenes are derived from the host genome
The search for activated oncogene
s:  the RAS gene familyComplex genomic rearrangements: the MYC gene family Proto-oncogene activation by gene amplification
Proto-oncogenes can be activated by chromosomal translocation
 
Chromosomal translocations in liquid tumors
Chronic myeloid leukemia and the Philadelphia chromosome
Oncogenic activation of transcription factors in Prostate cancer and Ewing’s sarcoma
Oncogene discovery in the genomic era: mutations in PIK3CASelection of tumor-associated mutations
Multiple modes of proto-oncogene activation
Oncogenes are dominant cancer genes
Germline mutations in RET and MET confer cancer predisposition
Proto-oncogene activation and tumorigenesis
 
Chapter 3:  Tumor Suppressor Genes What is a tumor suppressor gene?
The discovery of recessive cancer phenotypes
Retinoblastoma and Knudson’s two-hit hypothesis
Chromosomal localization of the retinoblastoma gene
The mapping and cloning of the retinoblastoma gene
Tumor suppressor gene inactivation: the second ‘hit’ and loss of heterozygosity
Recessive genes, dominant traitsAPC inactivation in inherited and sporadic colorectal cancers
TP53 inactivation: a frequent event in tumorigenesis
Functional inactivation of p53: tumor suppressor genes and oncogenes interact
Mutant TP53 in the germl
ine:  Li Fraumeni syndrome Ga
ins-of-function caused by cancer-associated mutations in TP53Cancer predisposition: allelic penetrance, relative risk and the odds ratio
Breast cancer susceptibility:  BRCA1 and BRCA2
Genetic losses on chromosome 9:  CDKN2A
Complexity at CDKN2A:  neighboring and overlapping genes
Genetic losses on chromosome 10:  PTEN
SMAD4 and the maintenance of stromal architecture
Two distinct genes cause neurofibromatosis From flies to humans, Patched proteins regulate developmental morphogenesis
von Hippel-Lindau disease
NOTCH1: tumor suppressor gene or oncogene?
Multiple endocrine neoplasia type 1
Most tumor suppressor genes are tissue-specific
Modeling cancer syndromes in mice
Genetic variation and germline cancer genes Tumor suppressor gene inactivation during colorectal tumorigenesis
Inherited tumor suppressor gene mutations: gatekeepers and landscapers
Maintaining the genome: caretakers
 
Chapter 4:  Genetic Instability and Cancer
What is genetic instability?
The majority of cancer cells are aneuploid Aneuploid cancer cells exhibit chromosome instability
Chromosome instability arises early in colorectal tumorigenesis
Chromosomal instability accelerates clonal evolution
Aneuploidy can result from mutations th
at directly impact mitosisSTAG2
andthe cohesion of sister chromatids Other genetic and epigenetic causes of aneuploidy
Transition from tetraploidy to aneuploidy during tumorigenesis  Multiple forms of genetic instability in cancer
Defects in mismatch repair cause hereditary nonpolyposis colorectal cancer
Mismatch repair-deficient cancers have a distinct spectrum of mutations
Defects in nucleotide excision repair cause xeroderma pigmentosum
NER syndromes: clinical heterogeneity and pleiotropy
DNA repair defects and mutagens define two steps towards genetic instability Defects in DNA crosslink repair cause Fanconi anemia
A defect in DNA double strand break responses causes ataxia-telangiectasia
A unique form of genetic instability underlies Bloom syndrome
Aging and cancer:  insights from the progeroid syndromes
Instability at the end: telomeres and telomerase
Overview: genes and genetic stability
  Chapter 5:  Cancer Genomes
Discovering the genetic basis of cancer: from genes to genomes
What types of genetic alterations are found in tumor cells?
How many genes are mutated in the various types of cancer?
What is the significance of the mutations that are found in cancers?
When do cancer-associated mutations occur?
How many different cancer genes are there? How many cancer genes are required for the development of cancer? Cance
r genetics shapes our understandingof metastasis Tumors are genetically heterogenous
Beyond the exome: the ‘dark matter’ of the cancer genome
A summary:  the genome of a cancer cell
 
Chapter 6:  Cancer Gene Pathways What are cancer gene pathways?
Cellular pathways are defined by protein-protein interactions
Individual biochemical reactions, multistep pathways, and networks
Protein phosphorylation is a common regulatory mechanism
Signals from the cell surface:  protein tyrosine kinases
Membrane-associated GTPases:  the RAS pathway
An intracellular kinase cascade: the MAPK pathway Genetic alterations of the RAS pathway in cancer
Membrane-associated lipid phosphorylation: the PI3K/AKT pathway
Control of cell growth and energetics:  the mTOR pathway
Genetic alterations in the PI3K/AKT and mTOR pathways define roles in cell survival
The STAT pathway transmits cytokine signals to the cell nucleus
Morphogenesis and cancer:  the WNT/APC pathway
Dysregulation of the WNT/APC pathway in cancers Notch signaling mediates cell-to-cell communication
Morphogenesis and cancer:  the Hedgehog pathway
TGF-/ SMAD signaling maintains adult tissue homeostasis
MYC is a downstream effector of multiple cancer gene pathways
activation is triggered by damaged or incompletelyreplicated chromosomes p53 is controlled b
y protein kinases encoded by tumor suppressor genes p53 induces the transcription of genes that suppress cancer phenotypes
Feedback loops dynamically control p53 abundance
The DNA damage signaling network activates interconnected repair pathways
Inactivation of the pathways to apoptosis in cancer
RB1 and the regulation of the cell cycle
Several cancer gene pathways converge on cell cycle regulators
Many cancer cells are cell cycle checkpoint-deficient Chromatin modification is recurrently altered in many types of cancer
Summary: putting together the puzzle 
 
Chapter 7:  Genetic Alternations in Common Cancers
Cancer genes cause diverse diseases
Cancer incidence and prevalence
Lung cancer
Prostate cancer
Breast cancer
Colorectal cancer
Endometrial cancer
Melanoma of the skin
Bladder cancer
Lymphoma
Cancers in the kidney
Thyroid cancer Leukemia
Cancer in the pancreas
Ovarian cancer
Cancers of the oral cavity and pharynx
Liver cancer
Cancer of the uterine cervix
Stomach cancer
Brain tumors  
Chapter 8: Cancer Genetics in the Clinic
The uses of genetic information
Elements of cancer risk:  carcinogens and genes
Identifying carriers o
f germline cancer genes Cance
r genes as biomarkers of early stage malignancies Cancer
genes as biomarkers for diagnosis, prognosis and recurrence Conventional anticancer therapies inhibit cell growth
Exploiting the loss of DNA repair pathways: synthetic lethality
On the horizon: achieving synthetic lethality in TP53-mutant cancers
Molecularly targeted therapy:  BCR-ABL and imatinib
Clonal evolution of therapeutic resistance
Targeting EGFR mutations
Antibody-mediated inhibition of receptor tyrosine kinases Inhibiting Hedgehog signaling
A pipeline from genetically-defined targets to targeted therapies
Neoantigens are recognized by the immune system
The future of oncology
Index
 

Notă biografică

Fred Bunz, M.D., Ph.D is a native of Long Beach, New York. He attended Stony Brook University and graduated from its Medical Scientist Training Program. His doctoral research in the enzymology of human DNA replication was conducted at Cold Spring Harbor Laboratory. Dr. Bunz completed a postdoctoral fellowship in Cancer Genetics at The Johns Hopkins University and the Howard Hughes Medical Institute, and now heads a laboratory at the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins that is focused on understanding the effects of DNA damage on cancer cells and normal cells. He lives in Baltimore with his wife, two children, a cat, and an Old English Sheepdog. 

Textul de pe ultima copertă

This is the second edition of a widely used  textbook that consolidates the basic concepts of the cancer gene theory and provides a framework for understanding the genetic basis of cancer. Particular attention is devoted to the origins of the mutations that cause cancer, and the application of evolutionary theory to explain how the cell clones that harbor cancer genes tend to expand. Focused on the altered genes and pathways that cause the growth of the most common tumors, Principles of Cancer Genetics is aimed at advanced undergraduates who have completed introductory coursework in genetics, biology and biochemistry, medical students and medical house staff.  For students with a general interest in cancer, this book provides a highly accessible and readable overview. For more advanced students contemplating future study in the field of oncology and cancer research, this concise book will be useful as a primer.

Caracteristici

A concise guide to understanding the genes that cause cancer
Illuminates the respective contributions of heredity, the environment, and errors in DNA replication
Relates cancer genes to the hallmark characteristics of the cancer cell
Provides an overview of the genetic etiology of common cancers
Highlights new frontiers in gene-based risk analysis, diagnosis and therapy
Includes supplementary material: sn.pub/extras

Descriere

Descriere de la o altă ediție sau format:
Cancer genetics is a field of daunting breadth and depth. The literature describes hundreds of genes and genetic alterations that are variably associated with again as many disease states and risk factors. Integrating these disparate pieces of highly specialized information is challenging for the professional scientist and student alike. Prinicples of Cancer Genetics consolidates the main concepts of the cancer gene theory, and provides a framework for understanding the genetic basis of cancer.
Focused on the most highly representative genes that underlie the most common cancers, Principles of Cancer Genetics is aimed at advanced undergraduates who have completed introductory courses in genetics, biology and biochemistry, medical students, and house medical house staff preparing for board examinations. Primary attention is devoted to the origins of cancer genes and the application of evolutionary theory to explain why the cell clones that harbor cancer genes tend to expand. The many points of controversy in cancer research are avoided, in favor of firmly established concepts. This book does not delve into tumor pathobiology beyond what is required to understand the role of genetic alterations in neoplastic growth. For students with a general interest in cancer, this book will provide a highly accessible overview. For students contemplating future study in the fields of oncology or cancer research, this book will be useful as a primer.

Recenzii

From the reviews:
“The book is exceptional in its clarity and scope of presentation. … Bunz focuses on a laser with short clear descriptions and presentations. … All in all a superb little gem worth being on many a desk. I find it is worth going back to from time to time.” (Philosophy, Religion and Science Book Reviews, bookinspections.wordpress.com, December, 2013)