By Scott H. Kaufmann MD, PhD (auth.), David A. Gewirtz, Shawn E. Holt, Steven Grant (eds.)
Apoptosis, Senescence and melanoma presents perception into proven practices and study into apoptosis and senescence through completely studying novel and rising suggestions and examine within the fields of mobilephone dying pathways, senescence development arrest, medications and resistance, DNA harm reaction, and different subject matters which nonetheless carry mysteries for researchers.
The quantity is split into six effortless to persist with sections. the 1st is Apoptosis and replacement Modes of mobilephone demise, by way of chapters on Telomeres and Telomerase, Senescence, Genomic Instability and Tumorigenesis. The 3rd half covers DNA harm reaction, Signaling Pathways and Tumorigenesis, whereas the fourth delves into Resistance and Sensitization. The ebook concludes with demonstrated melanoma cures and a piece which seems towards the long run with contemporary and constructing melanoma Therapies.
In overall, this quantity offers simple scientists and clinicians with a deeper and extra whole realizing of the mobile responses of malignancies that can ensure the effectiveness of therapy, either within the preliminary phases of the illness in addition to in disorder recurrence.
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Additional info for Apoptosis, Senescence, and Cancer
Frasch SC, Henson PM, Kailey JM, et al. Regulation of phospholipid scramblase activity during apoptosis and cell activation by protein kinase Cdelta. J Biol Chem 2000; 275:23065–73. 42. Martin SJ, Reutelingsperger CP, McGahon AJ, et al. Early redistribution of plasma membrane phosphatidylserine is a general feature of apoptosis regardless of the initiating stimulus: inhibition by overexpression of Bcl-2 and Abl. J Exp Med 1995; 182(5):1545–56. 43. Hanayama R, Tanaka M, Miwa K, Shinohara A, Iwamatsu A, Nagata S.
Stoka V, Turk B, Schendel SL, et al. Lysosomal protease pathways to apoptosis. Cleavage of bid, not pro-caspases, is the most likely route. J Biol Chem 2001; 276:3149–57. 99. Gajewski TF, Thompson CG. Apoptosis meets signal transduction: elimination of a BAD influence. Cell 1996; 87(4):589–92. 100. Puthalakath H, Huang DCS, O’Reilly LA, King SM, Strasser A. The proapoptotic activity of the Bcl-2 family member Bim is regulated by interaction with the dynein motor complex. Mol Cell 1999; 3:287–96.
In leukemia cell lines (248) and a substantial portion of mismatch repair-deficient colon and gastric cancers (249), the BAX gene is mutated, although the heterozygous nature of these mutations in clinical cancer (249) stands in contrast to results obtained in animal models (250) and by itself fails to completely account for any apoptotic defect. In other tumors, changes that upregulate the Akt pathway (251), including autocrine or paracrine activation of receptor tyrosine kinases, PI3KINASE gene mutation (252) or amplification (253), PTEN deletion, or AKT2 gene amplification (254), inhibit mitochondrial cytochrome c release (255).