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Updated: Sep 29, 2025

Modeling Spontaneous Metastatic Renal Cell Carcinoma mRCC in Mice Following Nephrectomy
Published on: April 29, 2014
Single-cell RNA-sequencing analysis reveals MYH9 promotes renal cell carcinoma development and sunitinib resistance
Zhipeng Xu1,2, Min Liu3, Jin Wang1,2
1Department of Urology, Shandong Qianfoshan Hospital, Cheeloo college of Medicine, Shandong University, Jinan, Shandong, China.
Abstract:
Clear cell renal cell carcinoma (ccRCC) is a serious threat to human health worldwide, while its heterogeneity limits therapeutic success and leads to poor survival outcomes. Single-cell RNA-sequencing (scRNA-seq) is an important technology, which provides deep insights into the genetic characteristics of carcinoma. In this study, we profiled the gene expression of single cells from human ccRCC tissues and adjacent normal tissues using the scRNA-seq. We found that MYH9 was commonly upregulated in the ccRCC cell subgroup. Additionally, MYH9 was of highly expression in ccRCC tissues and predicted poor prognosis of ccRCC patients. MYH9 knockdown in ccRCC cells dampened their proliferative and metastatic potentials, whereas MYH9 overexpression enhanced these properties. In vivo, MYH9 also promoted ccRCC growth. Mechanistic studies showed that MYH9 played these vital roles through AKT signaling pathway. Furthermore, MYH9/AKT axis determined the responses of ccRCC cells to sunitinib treatment and might serve as a biomarker for sunitinib benefits in ccRCC patients. Thus, MYH9 might be a novel therapeutic target and prognostic predictor for ccRCC.
Insights
Myosin-9 (MYH9) is upregulated in clear cell renal cell carcinoma (ccRCC), driving tumor growth and metastasis. Targeting MYH9 may improve ccRCC patient prognosis and sunitinib treatment response.
Area of Science:
- Oncology
- Molecular Biology
- Genomics
Background:
- Clear cell renal cell carcinoma (ccRCC) presents significant global health challenges due to tumor heterogeneity, impacting treatment efficacy and patient survival.
- Single-cell RNA sequencing (scRNA-seq) offers high-resolution insights into the complex genetic landscape of cancers like ccRCC.
Purpose of the Study:
- To investigate the role of gene expression in ccRCC using scRNA-seq.
- To identify potential therapeutic targets and prognostic biomarkers for ccRCC.
Main Methods:
- Profiling gene expression in single cells from human ccRCC and adjacent normal tissues via scRNA-seq.
- Analyzing the functional impact of MYH9 modulation on ccRCC cell proliferation and metastasis in vitro and in vivo.
- Investigating the mechanistic role of the MYH9/AKT signaling pathway.
Main Results:
- MYH9 was commonly upregulated in ccRCC cells and associated with poor patient prognosis.
- MYH9 knockdown reduced ccRCC cell proliferation and metastasis, while overexpression enhanced these traits.
- The MYH9/AKT axis was identified as a key pathway influencing ccRCC progression and sunitinib treatment response.
Conclusions:
- MYH9 is a potential therapeutic target and prognostic predictor for ccRCC.
- The MYH9/AKT axis influences ccRCC cell behavior and response to sunitinib therapy.
- Targeting MYH9 offers a promising strategy for improving ccRCC treatment outcomes.
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