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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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Abstract

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
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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Abstract

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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