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Oncogenomics handbook
Authors: ---
ISBN: 9781588294258 1588294250 9781592598939 9786610359288 1280359285 1592598935 Year: 2005 Publisher: Totowa, N.J. : Humana Press,

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Abstract

Bioinformatic integration of the findings from recent genomic and proteomic research has made possible the development of highly selective therapeutics that can target specific cellular pathways controlling cell proliferation, differentiation, metastasis, evasion of immune surveillance, angiogenesis, and apoptosis. In The Oncogenomics Handbook, a panel of internationally recognized researchers and clinicians provides an integrated overview of cancer drug discovery and development from the bench to the clinic, showing with broad strokes and representative examples the drug development process as a network of linked components leading from the discovered target to the ultimate therapeutic product. Following that path, the authors explain genomic databases and how to discover oncological targets from them, how then to advance from the gene and transcript to the level of protein biochemistry, how next to move from the chemical realm to that of the living cell and, ultimately, pursue animal modeling and clinical development. Emerging cancer therapeutics including rituximab, Herceptin®, Avastin™, ABGX-EGF, Velcade®, Iressa®, and Zevalin® are addressed. Additional chapters review clinical diagnostics, bioanalytics, and biomarkers and their importance to therapeutic outcome; detail antiangiogenic, supportive, immunomodulatory, and tumor-targeted approaches to cancer therapy; and provide a systems biology-bioinformatics overview of strategies and initiatives for the postgenomic era. Highlights include cancer genomics, transcriptomics, gene expression analysis, proteomic and enzymatic cancer profiling technologies, and cellular and animal approaches to cancer target validation. Authoritative and state-of-the-art, The Oncogenomics Handbook offers cancer researchers and drug developers a comprehensive update on the contribution of the genomic revolution to cancer drug discovery and development.


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P53
Authors: ---
ISBN: 1441982302 1441982310 Year: 2010 Publisher: Austin, Tex. : New York, New York : Landes Bioscience ; Springer Science+Business Media,

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Our understanding of human cancer in the past 40 years has been driven by linking innovative concepts and cutting edge technologies to key problems identified by clinical research. Some of the successes in cancer genetics identified from clinical work have been the identification of specific gene deletions in human chromosomes, the use of PCR-based cloning methodologies to identify and clone human cancer genes, the validation of the human cancer genes using transgenetic technologies in the mouse, and the ability to sequence whole genomes that has recently allowed a collation of all somatic and germline mutations in a human genome. In the same generation, entirely different disciplines involved in basic life science research have used model organisms like yeast, flies, worms, and cancer causing animal viruses as tools to develop windows to see into the machinery of the cell life cycle. The discoveries of pro-apoptotic genes, oncogenes, and covalent control mechanisms like phosphorylation and ubiquitination using the tools of science and technology have all been awarded Nobel prizes for their contribution to our understanding of how cells work. The discovery of p53 using the tumor causing animal virus SV40 falls into this pioneering period of biological and medical research.


Book
Diagnostic, prognostic and therapeutic value of gene signatures
Authors: --- ---
ISBN: 1617793574 9786613447685 1283447681 1617793582 Year: 2012 Publisher: New York : Humana Press,

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Gene expression studies have revealed diagnostic profiles and upregulation of specific pathways in many solid tumors. The explosion of new information in gene expression profiling could potentially lead to the development of tailored treatments in many solid tumors. In addition many studies are ongoing to validate these signatures also in predicting response to hormonal, chemotherapeutic and targeted agents in breast cancer as well as in other tumors.   Diagnostic, Prognostic and Therapeutic Value of Gene Signatures provides readers a useful and comprehensive resource about the range of applications of microarray technology in oncological diseases. Topics covered include gene signatures and soft tissue sarcomas, prognostic relevance of breast cancer signatures, gene expression profiling of colorectal cancer and liver metastasis, gene signatures in GISTs, CNVs and gene expression profiles in pancreatic cancer, and gene signatures in head/neck, lung and gastric tumors.   Diagnostic, Prognostic and Therapeutic Value of Gene Signatures will be of great value to residents and fellows, physicians, pathologists and  medical oncologists.


Book
Experimental and clinical metastasis : a comprehensive review
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ISBN: 1461436842 148999663X 1461436850 1283944804 Year: 2013 Publisher: New York : Springer,

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The primary cause of death related to cancers can be traced back to metastases, originated from cancer cells. The presence of metastatic disease, the spread of cancer cells, is the most important prognostic and survival factor in patients with cancer. Although treatment of the primary tumor is well established and usually results in local control, treating metastatic disease is a much more daunting task. At diagnosis, few patients present with clinically detectable metastatic lesions regardless of the clinical prognostic factor. Clinical trials assessing potential therapeutic agents are important in order to define the best specific treatment for a particular patient, which are the basis for patient-oriented research that eventually lead to personalized medicine. This volume aims to comprehensively present the latest research and information about metastasis. Understanding the mechanisms underlying the metastatic phenomenon could have vast implications for the large number of patients who are at a high risk for the development of metastasis.

Retroviruses and insights into cancer
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ISBN: 0387095802 9786612970986 1282970984 0387095810 1489981438 Year: 2011 Publisher: New York : Springer,

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Retroviruses cause chronic infections and insertion mutations in their hosts, often leading to the appearance of tumors. Studies of retrovirus-induced tumors have led to our understanding of many crucial concepts in cell and cancer biology, including the discoveries of reverse transcriptase, viral oncogenes, cellular proto-oncogenes and signal transduction pathways. This monograph provides an intriguing set of chapters on the many facets of retroviral involvement in cancers arising in a variety of organisms from fish to humans. Each chapter is written by experts in the field and relates recent work to previous experimental data. Retroviruses use many different mechanisms to induce cancers, ranging from activation of microRNAs, inactivation of tumor suppressor genes, activation or modifications of proto-oncogenes, as well as expression of viral proteins that manipulate cell signaling and the immune system. In recent years, retroviruses have been used as tools, not only for the characterization of cellular pathways, but also as vectors to deliver therapeutic or engineered genes. This knowledge is all the more startling due to the revelation that nearly 10% of the human genome consists of endogenous retroviruses, including many that are transcriptionally active. The emergence of new endogenous retroviruses causing lethal leukemias in koalas and, potentially, prostate cancer in humans ensures that the unique interactions of these viruses with their hosts will continue to fascinate and illuminate us.

Keywords

Carcinogenesis. --- Foreign workers --Germany (West). --- German language --Social aspects. --- German language --Syntax --Study and teaching --Foreign speakers. --- Grammar, Comparative and general. --- Language and languages --Variation. --- Retrovirus infections. --- Viral carcinogenesis. --- Retroviruses --- Oncogenic viruses --- Viral carcinogenesis --- RNA Viruses --- Vertebrate Viruses --- Genes --- Diseases --- Viruses --- Genome Components --- Genome --- Organisms --- Genetic Structures --- Genetic Phenomena --- Phenomena and Processes --- Retroviridae --- Oncogenic Viruses --- Genes, Neoplasm --- Neoplasms --- Biology --- Medicine --- Health & Biological Sciences --- Microbiology & Immunology --- Oncology --- Language and languages --- Grammar, Comparative and general --- German language --- Foreign workers --- Languages & Literatures --- Philology & Linguistics --- Variation --- Study and teaching --- Syntax --- Foreign speakers --- Social aspects --- Retroviruses. --- Oncogenic viruses. --- C-type RNA viruses --- Leukemogenic viruses --- Leukoviruses --- Oncornaviruses --- Oncoviruses --- RNA tumor viruses --- Cancer-causing viruses --- Cancer viruses --- Oncoviruses (Oncogenic viruses) --- Tumor viruses --- Tumorigenic viruses --- Medicine. --- Cancer research. --- Medical microbiology. --- Virology. --- Biomedicine. --- Cancer Research. --- Medical Microbiology. --- RNA viruses --- Microbial carcinogenesis --- Oncology. --- Medical virology. --- Microbiology. --- Medical microbiology --- Virology --- Virus diseases --- Tumors --- Microbial biology --- Microorganisms --- Microbiology --- Cancer research


Book
APC proteins
Authors: ---
ISBN: 1441911448 1461424518 1441911456 Year: 2009 Publisher: New York, N.Y. : Austin, Tex. : Springer Science+Business Media ; Landes Bioscience,

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The initial identification of the Adenomatous polyposis coli (Apc) gene as the site of mutations in familial adenomatous polyposis (FA P) was described in 1992. A causal relationship between Apc mutations and intestinal tract tumours was confirmed three years later with the establishment of the Min mouse model. These mice are heterozygous for Apc and develop numerous intestinal tumours that mimic FA P. Subsequently, Apc has emerged as the most commonly mutated gene in colorectal cancer with reports varying between 50-80 per cent of sporadic tumours carrying such mutations. The search for how m

Keywords

Adenomatous Polyposis Coli Protein. --- Adenomatous Polyposis Coli. --- Colon (Anatomy) -- Cancer. --- Colorectal Neoplasms -- Metabolism. --- Genes, APC. --- Tumor suppressor proteins. --- Colon (Anatomy) --- Tumor suppressor proteins --- Adenomatous Polyposis Coli --- Colorectal Neoplasms --- Genes, APC --- Metabolism --- Adenomatous Polyposis Coli Protein --- Intestinal Polyposis --- Intestinal Neoplasms --- Colonic Neoplasms --- Neoplastic Syndromes, Hereditary --- Colonic Diseases --- Metabolic Phenomena --- Cytoskeletal Proteins --- Genes, Tumor Suppressor --- Tumor Suppressor Proteins --- Rectal Diseases --- Adenomatous Polyps --- Proteins --- Neoplasm Proteins --- Intestinal Diseases --- Neoplasms --- Genes, Neoplasm --- Phenomena and Processes --- Gastrointestinal Neoplasms --- Genes, Recessive --- Adenoma --- Genetic Diseases, Inborn --- Gastrointestinal Diseases --- Digestive System Neoplasms --- Genes --- Diseases --- Neoplasms, Glandular and Epithelial --- Congenital, Hereditary, and Neonatal Diseases and Abnormalities --- Amino Acids, Peptides, and Proteins --- Chemicals and Drugs --- Digestive System Diseases --- Genome Components --- Neoplasms by Site --- Neoplasms by Histologic Type --- Genome --- Genetic Structures --- Genetic Phenomena --- Oncology --- Medicine --- Health & Biological Sciences --- Cancer --- Cancer. --- Antioncoproteins --- Growth suppressor proteins --- Metastasis suppressor proteins --- Colon cancer --- Colorectal cancer --- Medicine. --- Biomedicine. --- Biomedicine general. --- Clinical sciences --- Medical profession --- Human biology --- Life sciences --- Medical sciences --- Pathology --- Physicians --- Antioncogenes --- Health Workforce --- Biomedicine, general.


Book
Drugs for HER-2-positive breast cancer
Author:
ISBN: 3034600933 9786613080721 3034600941 1283080729 Year: 2011 Publisher: Basel [Switzerland] : Springer Basel AG,

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Growth factor receptors have long been known to drive malignant transformation and cancer progression. The epidermal growth factor receptor (EGFR, ErbB, HER) system is likely the best described membrane receptor tyrosine kinase family in malignant tumors. With implementation of the growth-inhibitory anti-HER-2 antibody trastuzumab (Herceptin) for the treatment of HER-2-positive advanced metastatic breast cancer, a new era has dawned in the therapy of this malignant disease. Unfortunately, trastuzumab-sensitive cancers invariably develop resistance to the antibody after some time. Recent clinical studies have revealed that these refractory tumors are still responsive to inhibition of the HER receptor family using dual HER-1/-2 inhibitors such as lapatinib (Tykerb/Tyverb). Moreover, a multiplicity of novel, improved irreversibly acting small molecular HER tyrosine kinase inhibitors are in the pipeline of many drug developing companies and are being evaluated in the clinical setting.

Keywords

BRCA genes. --- Breast -- Cancer -- Chemotherapy. --- Cancer -- Gene therapy. --- Trastuzumab. --- Trastuzumab --- BRCA genes --- Cancer --- Breast --- Antibodies --- Neoplasms by Site --- Genes, erbB --- Therapeutics --- Investigative Techniques --- Breast Diseases --- Biological Science Disciplines --- Therapeutic Uses --- Natural Science Disciplines --- Skin Diseases --- Analytical, Diagnostic and Therapeutic Techniques and Equipment --- Pharmacologic Actions --- Neoplasms --- Immunoglobulins --- Proto-Oncogenes --- Skin and Connective Tissue Diseases --- Immunoproteins --- Diseases --- Oncogenes --- Serum Globulins --- Chemical Actions and Uses --- Disciplines and Occupations --- Genes, Neoplasm --- Blood Proteins --- Chemicals and Drugs --- Globulins --- Proteins --- Genes --- Methods --- Antibodies, Monoclonal --- Breast Neoplasms --- Genes, erbB-2 --- Antineoplastic Agents --- Molecular Targeted Therapy --- Drug Therapy --- Pharmacology --- Amino Acids, Peptides, and Proteins --- Genome Components --- Genome --- Genetic Structures --- Genetic Phenomena --- Phenomena and Processes --- Medicine --- Health & Biological Sciences --- Oncology --- Pharmacy, Therapeutics, & Pharmacology --- Gene therapy --- Chemotherapy --- Cancer. --- Treatment. --- Cancer therapy --- Cancer treatment --- Therapy --- Medicine. --- Cancer research. --- Immunology. --- Antibodies. --- Pharmacology. --- Internal medicine. --- Oncology. --- Biomedicine. --- Pharmacology/Toxicology. --- Cancer Research. --- Internal Medicine. --- Toxicology. --- Oncology  . --- Monoclonal antibodies. --- Medicine, Internal --- Immunobiology --- Life sciences --- Serology --- Monoclonal immunoglobulins --- Molecular cloning --- Tumors --- Chemicals --- Poisoning --- Poisons --- Toxicology --- Immune globulins --- Immune serum globulin --- Blood proteins --- Plasma cells --- Antibody diversity --- Antigens --- Bacterial immunoglobulin-binding proteins --- Cancer research --- Drug effects --- Medical pharmacology --- Medical sciences --- Drugs --- Pharmacy --- Physiological effect

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