Genome Instability in Cancer Development by Ranga N. Venkatesan, Lawrence A. Loeb (auth.), Nathan Back, PDF

By Ranga N. Venkatesan, Lawrence A. Loeb (auth.), Nathan Back, Irun R. Cohen, David Kritchevsky, Abel Lajtha, Rodolfo Paoletti, Erich A. Nigg (eds.)

ISBN-10: 1402037635

ISBN-13: 9781402037634

ISBN-10: 1402037643

ISBN-13: 9781402037641

Research during the last many years has firmly tested the genetic foundation of melanoma. specifically, experiences on animal tumour viruses and chromosome rearrangements in human tumours have concurred to spot so-called ‘proto-oncogenes’ and ‘tumour suppressor genes’, whose deregulation promotes carcinogenesis. those very important findings not just clarify the prevalence of convinced hereditary tumours, yet additionally they set the degree for the advance of anti-cancer medicinal drugs that in particular objective activated oncogenes. in spite of the fact that, even with super growth in the direction of the elucidation of key signalling pathways occupied with carcinogenesis, cancer proceed to elude presently to be had treatments. This stands as a reminder that “cancer” is an awfully complicated affliction: even if a few cancers of the haematopoietic approach express just a constrained variety of attribute chromosomal aberrations, so much sturdy tumours exhibit a myriad of genetic adjustments and significant genetic heterogeneity. this can be idea to mirror a trait quite often often called ‘genome instability’, in order that no cancers are ever prone to show the very same genetic adjustments. Numerical and structural chromosome aberrations have been acknowledged as a trademark of human tumours for greater than a century. but, the motives and results of those aberrations nonetheless stay to be absolutely understood. specifically, the query of ways genome instability affects at the improvement of human cancers keeps to rouse extreme debate.

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Extra resources for Genome Instability in Cancer Development

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The relevance of bacterial mutators to understanding human cancer. In Cancer Surveys. Vol. 28. T. Lindahl, editor. Cold Spring Harbour Laboratory Press, Fairview, New York. 141-153. Mitelman, F. 1994. Catalog of Chromosome Aberrations in Cancer. Wiley-Liss, New York, NY. Modrich, P. 1995. Mismatch repair, genetic stability, and tumour avoidance. Philosoph. Transact. Royal Soc. 347:89-95. S. Sankaranand, S. Anant, M. Sugai, K. O. Davidson, and T. Honjo. 1999. Specific expression of activation-induced cytidine deaminase (AID), a novel member of the RNA-editing deaminase family in germinal centre B cells.

Med. Genet. 40:e60. Kraus J, Pantel K, Pinkel D, Albertson DG, Speicher MR (2003c) High-resolution genomic profiling of occult micrometastatic tumour cells. Genes Chromosomes Cancer 36:159166. 2. Monitoring Chromosome Rearrangements 39 Lacoste TD, Michalet X, Pinaud F, Chemla DS, Alivisatos AP, Weiss S (2000) Ultrahighresolution multicolour colocalization of single fluorescent probes. Proc. Natl. Acad. Sci. USA. 97:9461-9466. Landegent JE, Jansen in de Wal N, Dirks RW, Baas F, van der Ploeg M (1987) Use of whole cosmid cloned genomic sequences for chromosomal localization by non-radioactive in situ hybridization.

MONITORING CHROMOSOME REARRANGEMENTS AND CHROMOSOMAL INSTABILITY OR THE DIFFERENCE BETWEEN “STATE” AND “RATE” Currently there is a plethora of technologies available for chromosome analyses. However, it is important to keep in mind that there are fundamental differences whether the presence of chromosomal rearrangements or whether chromosomal instability is to be investigated. The existence of genetic alterations in a tumour, such as chromosomal rearrangements, even when frequent, does not mean that the tumour is genetically unstable.

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Genome Instability in Cancer Development by Ranga N. Venkatesan, Lawrence A. Loeb (auth.), Nathan Back, Irun R. Cohen, David Kritchevsky, Abel Lajtha, Rodolfo Paoletti, Erich A. Nigg (eds.)

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