Tyrosine Kinase Inhibitors associated muscle complaints like cramps, pain, and weakness are a few of the concerns contributing to declined disease control and quality of life. In this study, we investigated whether Ponatinib, a 3rd generation TKI, induces muscle toxicity in both In Vitro and In Vivo models and expand BMP-7 as a possible treatment option for its attenuation. For the In vitro study, Sol-8, a mouse myogenic cell line was exposed to Ponatinib and BMP-7 for 24hrs each. For the In vivo study, C57BL/6J mice were injected and euthanized after 14 days. The soleus muscle was isolated and used for experimentation. Both the studies were conducted with 3 groups: Control, Ponatinib, and Ponatinib+BMP-7. Ponatinib-induced muscle toxicity via apoptosis was established by TUNEL Assay, pro-apoptotic markers- Caspase 3, BAX, and anti-apoptotic marker Bcl2 via Immunocytochemistry and Immunohistochemistry. For the In vivo study, further confirmations of the above-mentioned apoptotic markers were done by RT-PCR. Ponatinib-induced muscle myopathy and loss in muscle function were also determined along with the effect on apoptotic pathway proteins PTEN and AKT. A significant (p < 0.05) increase in apoptotic positive nuclei as well as positive cells for pro-apoptotic markers was observed in Ponatinib treatment groups both in vitro and in vivo along with loss of muscle function and adverse muscle remodeling. Whereas BMP-7 treatment significantly (p < 0.05) attenuated Ponatinib-induced apoptosis, restored muscle function, and improved muscle remodeling. The result of our study suggests that Ponatinib-induces apoptotic cell death in skeletal cells which was attenuated by BMP-7.
Identifer | oai:union.ndltd.org:ucf.edu/oai:stars.library.ucf.edu:etd2020-2294 |
Date | 01 January 2022 |
Creators | Srivastava, Ayushi |
Publisher | STARS |
Source Sets | University of Central Florida |
Language | English |
Detected Language | English |
Type | text |
Format | application/pdf |
Source | Electronic Theses and Dissertations, 2020- |
Page generated in 0.0019 seconds