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Genomic Alterations of Anaplastic Lymphoma Kinase May Sensitize Tumors to Anaplastic Lymphoma Kinase Inhibitors McDermott  et. al.  Cancer Research. 2008; 68 (9) 3389-3395 Juliane Carvalho Johns Hopkins University Cancer Biology: AS410_638_81_SP10 Prof: Elena Tilli Shiffert, PhD. Online presentation: February 16, 2009
Outline ,[object Object],[object Object],[object Object],[object Object],[object Object]
Anaplastic Lymphoma Kinase (ALK) ,[object Object],[object Object],[object Object],[object Object],Biochemical Journal (2009) Volume  420 , 345-361
ALK cont’d ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Materials and Methods ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Figure 1. A, pie chart representation of the sensitivity of 602 human cancer cell lines to treatment with 200 nmol/L TAE684 Copyright ©2008 American Association for Cancer Research McDermott, U. et al. Cancer Res 2008;68:3389-3395
Copyright ©2008 American Association for Cancer Research McDermott, U. et al. Cancer Res 2008;68:3389-3395 Figure 2. A, FISH analysis of the BE(2)-C, KELLY, and NB-1 neuroblastoma cell lines using the LSI ALK Dual Color, Break Apart Rearrangement Probe
Copyright ©2008 American Association for Cancer Research McDermott, U. et al. Cancer Res 2008;68:3389-3395 Figure 3. A, pie chart representation of the sensitivity of 256 human cancer cell lines to 200 nmol/L of the IGF-IR inhibitor BMS-536924 following 72 h of treatment
Copyright ©2008 American Association for Cancer Research McDermott, U. et al. Cancer Res 2008;68:3389-3395 Figure 4. A, dose-response curves showing the effect of the ALK inhibitor TAE684 and the MET/ALK inhibitor PF-2341066 on cell viability 72 h after treatment in the SU-DHL-1 and Karpas-299 lymphoma cell lines and the NB-1 neuroblastoma cell line
Conclusions  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Questions
Literature consulted ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

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Juliane Carvalho Cancer Biology Presentation

  • 1. Genomic Alterations of Anaplastic Lymphoma Kinase May Sensitize Tumors to Anaplastic Lymphoma Kinase Inhibitors McDermott et. al. Cancer Research. 2008; 68 (9) 3389-3395 Juliane Carvalho Johns Hopkins University Cancer Biology: AS410_638_81_SP10 Prof: Elena Tilli Shiffert, PhD. Online presentation: February 16, 2009
  • 2.
  • 3.
  • 4.
  • 5.
  • 6. Figure 1. A, pie chart representation of the sensitivity of 602 human cancer cell lines to treatment with 200 nmol/L TAE684 Copyright ©2008 American Association for Cancer Research McDermott, U. et al. Cancer Res 2008;68:3389-3395
  • 7. Copyright ©2008 American Association for Cancer Research McDermott, U. et al. Cancer Res 2008;68:3389-3395 Figure 2. A, FISH analysis of the BE(2)-C, KELLY, and NB-1 neuroblastoma cell lines using the LSI ALK Dual Color, Break Apart Rearrangement Probe
  • 8. Copyright ©2008 American Association for Cancer Research McDermott, U. et al. Cancer Res 2008;68:3389-3395 Figure 3. A, pie chart representation of the sensitivity of 256 human cancer cell lines to 200 nmol/L of the IGF-IR inhibitor BMS-536924 following 72 h of treatment
  • 9. Copyright ©2008 American Association for Cancer Research McDermott, U. et al. Cancer Res 2008;68:3389-3395 Figure 4. A, dose-response curves showing the effect of the ALK inhibitor TAE684 and the MET/ALK inhibitor PF-2341066 on cell viability 72 h after treatment in the SU-DHL-1 and Karpas-299 lymphoma cell lines and the NB-1 neuroblastoma cell line
  • 10.
  • 12.