Although vehicle-treated p53 +/− mice showed a trend towards increased survival compared with ABT-737-treated p53 +/− animals (median survival: vehicle=469 days versus ABT-737=312 days), this difference did not reach statistical significance ( P =0.0623).
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Pharmacological blockade of Bcl-2, Bcl-x(L) and Bcl-w by the BH3 mimetic ABT-737 has only minor impact on tumour development in p53-deficient mice.
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