The present invention provides novel compositions and methods for use in
the treatment of cancer, specifically, in the treatment of chronic
myelogenous leukemia (CML). The compositions contain antisense
oligonucleotides that hybridize to Grb2 and Crkl nucleic acids, the gene
products of which are known to interact with the tumorigenic protein
bcr-abl. Used alone, in conjunction with each other, and even in
conjunction with antisense oligonucleotides directed to bcr-abl nucleic
acids, these compositions inhibit the proliferation of CML cancer cells.