MITF Promotes Cell Growth, Migration and Invasion in Clear Cell Renal Cell Carcinoma by Activating the RhoA/YAP Signal Pathway

• Published in: Cancers Vol. 13; no. 12; p. 2920
• Main Authors: Kim, Nayoung, Kim, Solbi, Lee, Myung-Won, Jeon, Heung-Jin, Ryu, Hyewon, Kim, Jin-Man, Lee, Hyo-Jin
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 11-06-2021; MDPI
• Subjects: Antibodies; Biotechnology; Cell cycle; Cell growth; Cell migration; Cell proliferation; Clear cell-type renal cell carcinoma; Cloning; Helix-loop-helix proteins (basic); Invasiveness; Kidney cancer; Leucine zipper proteins; Liver cancer; Mast cells; Medical prognosis; Melanocytes; Melanoma; Microphthalmia-associated transcription factor; Osteoclasts; Pancreas; Pancreatic carcinoma; Plasmids; RhoA protein; Signal transduction; Therapeutic applications; Therapeutic targets; Wound healing; Yes-associated protein; United States > US
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers13122920

Microphthalmia-associated transcription factor (MITF) is a basic helix-loop-helix leucine zipper transcription factor involved in the lineage-specific regulation of melanocytes, osteoclasts and mast cells. MITF is also involved in the progression of melanomas and other carcinomas, including the liver, pancreas and lung. However, the role of MITF in clear cell renal cell carcinoma (ccRCC) is largely unknown. This study investigates the functional role of MITF in cancer and the molecular mechanism underlying disease progression in ccRCC. MITF knockdown inhibited cell proliferation and shifted the cell cycle in ccRCC cells. In addition, MITF knockdown reduced wound healing, cell migration and invasion compared with the controls. Conversely, MITF overexpression in SN12C and SNU482 cells increased cell migration and invasion. Overexpression of MITF activated the RhoA/YAP signaling pathway, which regulates cell proliferation and invasion, and increased YAP signaling promoted cell cycle-related protein expression. Additionally, tumor formation was impaired by MITF knockdown and enhanced by MITF overexpression in vivo. In summary, MITF expression was associated with aggressive tumor behavior, and increased the migratory and invasive capabilities of ccRCC cells. These effects were reversed by MITF suppression. These results suggest that MITF is a potential therapeutic target for the treatment of ccRCC.