Supplementary information
From the following article:
Survival signalling by Akt and eIF4E in oncogenesis and cancer therapy
Hans-Guido Wendel, Elisa de Stanchina, Jordan S. Fridman, Abba Malina, Sagarika Ray, Scott Kogan, Carlos Cordon-Cardo, Jerry Pelletier and Scott W. Lowe
Nature 428, 332-337(18 March 2004)
doi:10.1038/nature02369
Supplementary Figure 1
Representative data from flow cytometric immunophenotyping of control (myc), Bcl-2 (myc/bcl-2), Akt (myc/akt) and eIF4E (myc/eIF4E) tumours.
Supplementary Figure 2
Allele-specific PCR to detect the wild-type (p53 WT) and mutant allele (p53 Neo) in tumours derived from E
-myc/p53+/- HSCs.
Supplementary Figure 3
Kaplan-Meier plots detailing the survival time following treatment with CTX (a) and DXR (b).
Supplementary Figure 4
Overall survival of mice treated with rapamycin alone or in combination with conventional chemotherapy.
Supplementary Figure 5
Kaplan-Meier analysis of tumour free survival in Akt tumour bearing mice (a) following treatment with CTX (n = 16, red), RAP (n = 12, blue), or CTX+RAP (C+R, n = 8) and in Bcl-2 tumour bearing mice (b) treated with CTX (n = 6, red), RAP (n = 6, blue) and CTX+RAP (C+R, n=4, green).
Supplementary Figure 6
Rapamycin reverses chemoresistance in matched Akt-expressing lymphomas.
Supplementary Figure 7
Quantification of eIF4E expression in lysates derived from Bcl-2 (n=3), Akt (n=5) and eIF4E (n=5) tumours.
Supplementary Table 1
Immunophenotype of Emmyc tumours expressing Akt, Bcl-2 or eIF4E. PDF, 168kB
Supplementary Figure Legends
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