Browsing by Subject "EMT"
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Item Analysis of Key Cellular Changes of Triple Negative Breast Cancer Cells in Response to Kinase-Inhibiting BI2536 and Associated Derivatives(2023-05) Baker, Christopher V.; Bunnell, Bruce A.; Burow, Matthew; Chaudhary, PankajPurpose: Triple Negative Breast Cancer (TNBC) is a subtype of breast cancer that grows quickly and has higher rates of metastasis and reoccurrence relative to other Breast Cancer subtypes that make it, in general, a much more dangerous subtype of breast cancer. The Kinase Chemogenomic Set (KCGS) is a collection of 187 kinase-inhibiting compounds with broad activity across 215 different kinases. We hypothesize that this plate contains compounds with the potential to inhibit TNBC and that exploring the transcriptomic and proteomic changes in TNBC cells may give insights into novel treatment targets. Methods: To test this hypothesis, we have utilized two main cell lines, the MDA-MB-231 line and a patient-derived xenograft line, the TuX-BxC-4IC cell line. Measurements have been taken at various time points up until 72 hours at various concentrations of a compound of interest, BI2536, between 1nM and 1uM. Primarily, data will be collected using qRT-PCR to gain insight into the transcriptomic changes during the potential EMT changes. Additionally, various other experiments related to migration, staining, and other essential markers will be conducted on the compound of interest and derivatives of the compound. Results: Initial results and prior work indicate that the compound of interest has moderate success in slowing cancer cell growth. Additionally, initial findings indicate that the compound may succeed in halting and potentially even reversing the EMT process. Conclusion: With this primary data set, we believe that the kinases targeted by the compound may hold potential key targets for the treatment of TNBC.Item Dissecting the Role of Protein Kinase C-Epsilon in Breast Cancer(2013-12-01) Jain, Kirti; Basu, AlakanandaProtein kinase C-epsilon (PKCε) has pro-tumor functions in many cancers including breast cancer. The purpose of this dissertation is to understand the role of PKCε in fundamental processes that are associated with breast cancer development and progression. PKCε is known to promote the survival of breast cancer cells. Autophagy is a process of cellular self-digestion that can mediate cell survival during stress. We have found that PKCε overexpression increases the basal autophagy in breast cancer cells while its depletion reduces it. Moreover, the effect of PKCε on autophagy is isozyme specific. Regulation by PKCε is not limited to basal autophagy as it also mediated starvation-induced autophagy. Looking for the possible mechanisms, we found that PKCε negatively regulates mammalian target of rapamycin (mTOR), which is the master regulator of autophagy. These results show that PKCε positively regulates autophagy, likely, via inhibition of mTOR. PKCε overexpression in mammary epithelial cells led to morphological changes indicating its role in regulation of cell plasticity. Further analysis revealed that PKCε promotes epithelial to mesenchymal transition (EMT), which is an early step in cancer metastasis. In addition, PKCε mediated transforming growth factor-beta (TGFβ)-induced EMT partially via Snail, which is a crucial EMT effector. Moreover, PKCε promoted cell migration and anoikis Ii resistance which are hallmarks of EMT. To examine the phenotypic effect of PKCε manipulation in a physiologically relevant context, we employed three dimensional (3D) cell culture model. We found that PKCε overexpression led to disruption of acinar morphogenesis in 3D culture. These results indicate a causal role for PKCε in breast tumor development and progression