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Fig. 4 | Molecular Cancer

Fig. 4

From: CDK6-PI3K signaling axis is an efficient target for attenuating ABCB1/P-gp mediated multi-drug resistance (MDR) in cancer cells

Fig. 4

Cross-downregulation of CDK6-PI3K axis in the cdk6-deficient KB-C2 cells reduced the expression of ABCB1 by inducing responsive alternative splicing (AS) in the pre-mRNA of ABCB1. A Relative expression of the functional proteins including CDK6, CDK4, ABCB1, PIK3CA and PIK3CB in KB-C2 and the cdk6-deficient KB-C2 cell populations. Major transcripts according to each intact protein were calculated in the cells expressing identical level of GAPDH. B Heatmap showed that through AS of pre-mRNA in response to cdk6 deletion, the level of the transcripts expressing functional ABCB1 protein was significantly downregulated whereas some transcripts expressing truncated inactive ABCB1 peptides (e.g., ENST00000488737) were upregulated in the KB-C2 cells with deleted cdk6 gene. C Differential expression heatmap showing downregulation of PI3K 110α and 110β (encoded by PIK3CA and PIK3CB genes, respectively) in the KB-C2-k.o.cdk6 population as compared with the non-gene deficient KB-C2 cells. D Protein-protein interaction network showing the pathways linking the differently expressed proteins in the KB-C2 cells with deficiency of cdk6. This network reflects the factors that have most intimate relationships with CDK6, and the pathways that are regulated by deletion of cdk6 and belong to different biological functions. Yellow represents the protein with no significant difference in expression. From green to blue, the downregulation of proteins is gradually obvious. From orange to red, the up regulation of proteins is gradually obvious

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