Investigation Of The C-Met Signaling Pathway In A Renal Carcinoma Cancer Cell Line
Project no. 32855 · Status: Kapanmış (Yayın bekleniyor) · 2025
Summary
<p class="ql-align-justify">Cancer is rapidly increasing today. Renal cell carcinoma (RCC) is one of the 10 most common and widespread cancers worldwide. It is the most common type of kidney cancer in adults, accounting for approximately 90–95% of cases. Although surgical resection is the primary curative approach for RCC, a significant number of patients experience disease recurrence. In this context, the development of targeted therapies—such as tyrosine kinase inhibitors (TKIs), mammalian target of rapamycin (mTOR) inhibitors, and immune checkpoint inhibitors—has marked a significant turning point in the treatment of metastatic renal cell carcinoma. As research into the biology of human neoplasms has increased, molecularly targeted agents—which generally demonstrate higher efficacy and lower toxicity—have been replacing traditional cytotoxic and cytostatic regimens in cancer treatment over the past decade. This trend is significantly impacting treatment options. In this context, our study investigating the c-Met pathway in a renal carcinoma cell line will identify potential implications for cancer biology and treatment strategies. The c-Met pathway is responsible for cell proliferation, growth, invasion, cell migration, proliferation, and the cell cycle. Its irregular activation leads to the formation of cancer cells and promotes their proliferation and growth. The c-Met protein is a transmembrane receptor tyrosine kinase. Its only known ligand, hepatocyte growth factor (HGF)/spread factor (SF), regulates cell growth, migration, invasion, proliferation, and angiogenesis. This project focuses on understanding the molecular mechanisms of the c-Met signaling pathway in a renal carcinoma cell line. The study will analyze the effects of c-Met inhibition on cell proliferation, gene expression profiles, and apoptosis. To this end, c-Met inhibitors such as foretinib will be used. Cell culture experiments will be conducted to assess cell viability, cell proliferation, and real-time quantitative polymerase chain reaction. In addition, cell viability and proliferation will be measured using appropriate kits, and cellular changes will be evaluated through apoptosis analysis. Gene expression will be assessed via qPCR. The expected results indicate that c-Met may be an effective target in the treatment of renal carcinoma.</p><p></p><p></p><p></p><p></p><p></p><p></p>