Download Advances in Biology and Therapy of Multiple Myeloma: Volume by Esteban Braggio Ph.D., Rafael Fonseca M.D. (auth.), Nikhil PDF

By Esteban Braggio Ph.D., Rafael Fonseca M.D. (auth.), Nikhil C. Munshi, Kenneth C. Anderson (eds.)

Despite the advances in traditional, novel agent and excessive dose chemotherapy a number of myeloma (MM) is still incurable. to be able to triumph over resistance to present cures and enhance sufferer consequence, novel biologically-based remedy methods are being constructed. present translational study in MM concentrating on the improvement of molecularly-based mix cures has nice promise to accomplish excessive frequency and sturdy responses within the majority of sufferers. significant advances are making this objective attainable. First, contemporary advances in genomics and proteomics in MM have allowed for elevated figuring out of disorder pathogenesis, pointed out novel healing ambitions, allowed for molecular category, and supplied the clinical cause for combining specific treatments to extend tumor mobile cytotoxicity and abrogate drug resistance. moment, there's now an elevated knowing of ways adhesion of MM cells in bone marrow (BM) extra affects gene expression in MM cells, in addition to in BM stromal cells (BMSCs). because of those advances in oncogenomics at the one hand and elevated realizing of the position of the BM within the pathogenesis of MM at the different, a brand new remedy paradigm concentrating on the tumor telephone and its BM microenvironment to beat drug resistance and increase sufferer consequence has now been constructed. Thalidomide, lenalidomide, and Bortezomib are 3 brokers which goal the tumor mobile in its microenvironment in either laboratory and animal types and that have swiftly translated from the bench to the bedside. Ongoing efforts are utilizing oncogenomics and mobile signaling reviews to spot subsequent new release of cures in MM at the one hand, and to notify the layout of mixture trials at the different. This new paradigm for overcoming drug resistance and enhancing sufferer end result in MM has nice promise not just to alter the common historical past of MM, but in addition to function a version for specified therapeutics directed to enhance consequence of sufferers with MM.

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Extra resources for Advances in Biology and Therapy of Multiple Myeloma: Volume 1: Basic Science

Sample text

Cancer Res 55:3854–3859 10. Drach J, Angerler J, Schuster J et al (1995) Interphase fluorescence in situ hybridization identifies chromosomal abnormalities in plasma cells from patients with monoclonal gammopathy of undetermined significance. Blood 86:3915–3921 11. Zandecki M, Laï JL, Genevieve F et al (1997) Several cytogenetic subclones may be identified within plasma cells from patients with monoclonal gammopathy of undetermined significance, both at diagnosis and during the indolent course of this condition.

Fonseca R, Harrington D, Oken MM et al (2002) Biological and prognostic significance of interphase fluorescence in situ hybridization detection of chromosome 13 abnormalities (delta13) in multiple myeloma: an eastern cooperative oncology group study. Cancer Res 62:715–720 75. Drach J, Ackermann J, Fritz E et al (1998) Presence of a p53 gene deletion in patients with multiple myeloma predicts for short survival after conventional-dose chemotherapy. Blood 92:802–809 76. Tiedemann RE, Gonzalez-Paz N, Kyle RA et al (2008) Genetic aberrations and survival in plasma cell leukemia.

MM patients are characterized by highly frequent (>30%) gain of the odd numbered chromosomes 3, 5, 7, 9, 11, 15, 19, and 21, loss of chromosomes 13 and X (in females cases), and gain of 1q and frequent (>10%) deletion of sub-chromosomal material including 1p, 6q, 8p, 12p, 14q, 16p, 16q, and 20p and gain of 6p. Based on these frequent CNAs, MM are clustered into several groups, with one predominant group including the vast majority of hyperdiploid MM (³47 chromosomes) that almost exclusively harbored chromosome gains (whole or segmental) [2].

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