Lysine methyltransferase 5C increases the proliferation and metastatic abilities of clear cell renal cell carcinoma
Bohan Zeng1, Runlan Wan2, Kun Chang1
1Department of Urology, Fudan University Shanghai Cancer Center, Shanghai 200032, P.R. China.
International Journal of Oncology
|March 1, 2024
Summary
Lysine methyltransferase 5C (KMT5C) is elevated in clear cell renal cell carcinoma (ccRCC), promoting cancer growth and metastasis. Targeting KMT5C may offer new therapeutic strategies for ccRCC patients.
Area of Science:
- Oncology
- Epigenetics
- Molecular Biology
Background:
- Clear cell renal cell carcinoma (ccRCC) is an aggressive kidney cancer subtype with high metastasis and recurrence rates.
- Histone modifications, including H4K20 trimethylation by Lysine methyltransferase 5C (KMT5C), are crucial in cancer development.
- The specific role of KMT5C in ccRCC pathogenesis is not well understood.
Purpose of the Study:
- To investigate the expression and functional role of KMT5C in clear cell renal cell carcinoma.
- To determine if KMT5C influences key cancer processes like proliferation, epithelial-mesenchymal transition (EMT), and glycolysis in ccRCC.
Main Methods:
- KMT5C expression levels were compared between ccRCC tissues and normal tissues.
- ccRCC cell lines with reduced KMT5C expression were established to study its function.
- The impact of KMT5C on glycolytic genes, proliferation, and EMT-associated transcription factors was analyzed.
Main Results:
- KMT5C expression was significantly upregulated in ccRCC tissues and correlated with poorer patient survival.
- KMT5C knockdown in ccRCC cells reduced aerobic glycolysis by regulating key glycolytic genes.
- KMT5C promoted ccRCC cell proliferation and epithelial-mesenchymal transition (EMT) by controlling critical transcription factors.
Conclusions:
- KMT5C acts as an oncoprotein in ccRCC, driving tumor growth and progression.
- KMT5C levels may serve as a biomarker for molecular diagnosis of ccRCC.
- KMT5C represents a potential therapeutic target for developing novel treatment strategies for ccRCC.
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