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FIGURE 5.2
Schema showing the effects of miR-100 on the Akt/mTOR pathway and
-tubulin isotypes.
MiR-100 was shown to reduce levels of phosphorylated Akt and mTOR, signals implicated in
tumor progression ( Nagaraja et al., 2010 ). In MCF7 breast cancer cells, miR-100 regulates
b
b
-tubulin isotype classes I, IIA, and V ( Lobert et al., 2011 ). Paclitaxel treatment reduces
miR-100, and this result has implications for drug resistance and the potential for
b
-tubulin
isotypes to be used as biomarkers for tumor progression.
FIGURE 5.3
Comparative qRT-PCR for miR200c. MDA-MB-231 cells were treated with 40 nM paclitaxel
for 24 h. Data were normalized to SCA17 as the housekeeping gene.
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