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Updated: Jul 7, 2025

Comparing Metastatic Clear Cell Renal Cell Carcinoma Model Established in Mouse Kidney and on Chicken Chorioallantoic Membrane
Published on: February 8, 2020
FOXM1/KIF20A axis promotes clear cell renal cell carcinoma progression via regulating EMT signaling and affects
Kai Fang1, Min Gong1, Dong Liu1
1Department of Urology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Background:
The correlation between FOXM1 and KIF20A has not been revealed in clear cell renal cell carcinoma (ccRCC).
Methods:
Public data was downloaded from The Cancer Genome Atlas (TCGA) database. R software was utilized for the execution of bioinformatic analysis. The expression levels of specific molecules (mRNA and protein) were detected using real-time quantitative PCR (qRT-PCR) and Western blot assays. The capacity of cell growth was assessed by employing CCK8 and colony formation assay. Cell invasion and migration ability were assessed using transwell assay.
Results:
In our study, we illustrated the association between FOXM1 and KIF20A. Our results indicated that both FOXM1 and KIF20A were associated with poor prognosis and clinical performance. The malignant characteristics of ccRCC cells can be significantly suppressed by inhibiting FOXM1 and KIF20A, as demonstrated by in vitro experiments. Moreover, we found that FOXM1 can upregulate KIF20A. Then, EMT signaling was identified as the underlying pathway FOXM1 and KIF20A are involved. WB results indicated that FOXM1/KIF20A axis can activate EMT signaling. Moreover, we noticed that FOXM1 and KIF20A can affect the immunotherapy response and immune microenvironment of ccRCC patients.
Conclusions:
Our results identified the role of the FOXM1/KIF20A axis in ccRCC progression and immunotherapy, making it the underlying target for ccRCC.
Insights
The FOXM1/KIF20A axis promotes clear cell renal cell carcinoma (ccRCC) progression and impacts immunotherapy response. Inhibiting this axis suppresses ccRCC malignancy and offers a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- The relationship between Forkhead box protein M1 (FOXM1) and Kinesin family member 20A (KIF20A) in clear cell renal cell carcinoma (ccRCC) remains underexplored.
- Understanding novel molecular correlations is crucial for advancing ccRCC treatment strategies.
Purpose of the Study:
- To elucidate the correlation between FOXM1 and KIF20A in ccRCC.
- To investigate the functional role of the FOXM1/KIF20A axis in ccRCC progression and its impact on immunotherapy.
Main Methods:
- Bioinformatic analysis of The Cancer Genome Atlas (TCGA) database.
- Quantitative real-time PCR (qRT-PCR) and Western blot for gene and protein expression.
- In vitro assays (CCK8, colony formation, Transwell) to assess cell growth, invasion, and migration.
- Analysis of the epithelial-mesenchymal transition (EMT) signaling pathway.
Main Results:
- FOXM1 and KIF20A expression are significantly associated with poor prognosis and clinical progression in ccRCC.
- Inhibition of FOXM1 and KIF20A effectively suppresses ccRCC cell malignancy in vitro.
- FOXM1 positively regulates KIF20A expression, and this axis activates EMT signaling.
- The FOXM1/KIF20A axis influences the tumor immune microenvironment and immunotherapy response in ccRCC.
Conclusions:
- The FOXM1/KIF20A axis plays a critical role in ccRCC progression and is implicated in modulating immunotherapy outcomes.
- Targeting the FOXM1/KIF20A axis presents a promising therapeutic strategy for ccRCC treatment.
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