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Updated: Dec 25, 2025

Comparing Metastatic Clear Cell Renal Cell Carcinoma Model Established in Mouse Kidney and on Chicken Chorioallantoic Membrane
Published on: February 8, 2020
Lactotransferrin Downregulation Drives the Metastatic Progression in Clear Cell Renal Cell Carcinoma
I-Jen Chiu1,2, Yung-Ho Hsu2,3, Jeng-Shou Chang4
1Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, 250 Wu-Hsing Street, Taipei 11031, Taiwan.
Abstract:
: Clear cell renal cell carcinoma (ccRCC) is the main type of RCC, which is the most common type of malignant kidney tumor in adults. A subpopulation (>30%) of ccRCC patients develop metastasis; however, the molecular mechanism remains largely unknown. Here, we found that LTF, the gene encoding lactotransferrin, is dramatically downregulated in primary tumors compared to normal tissues derived from ccRCC patients deposited in The Cancer Genome Atlas (TCGA) database and is a favorable prognostic marker. Moreover, LTF downregulation appears to be more dominant in metastatic ccRCC. LTF overexpression suppresses migration ability in A498 ccRCC cells with high metastatic potential, whereas LTF knockdown fosters cellular migration in poorly metastatic ccRCC cells. Gene set enrichment analysis demonstrated that LTF expression inversely correlates with the progression of epithelial-mesenchymal transition (EMT) in ccRCC, which was further confirmed by RT-PCR experiments. Therapeutically, the administration of recombinant LTF protein significantly suppresses the cell migration ability and lung metastatic potential of ACHN cells, as well as LTF-silenced A498 cells. The gene knockdown of lipoprotein receptor-related protein 1 (LRP1) robustly blocked recombinant LTF protein-induced inhibition of cellular migration and gene expression of EMT markers in ACHN cells. LTF downregulation and LRP1 upregulation combined predicted a poor overall survival rate in ccRCC patients compared to that with either factor alone. Our findings uncover a new mechanism by which LTF may interact with LRP1 to inhibit metastatic progression in ccRCC and also reveal the therapeutic value of recombinant LTF protein in treating metastatic ccRCC.
Insights
Lactotransferrin (LTF) is downregulated in metastatic kidney cancer, hindering its progression. Recombinant LTF protein shows therapeutic potential by inhibiting cancer cell migration and metastasis, possibly via LRP1 interaction.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Clear cell renal cell carcinoma (ccRCC) is the most common kidney cancer.
- Metastasis occurs in over 30% of ccRCC patients, with unknown molecular drivers.
- Lactotransferrin (LTF) is a potential tumor suppressor in ccRCC.
Purpose of the Study:
- Investigate the role of LTF in ccRCC metastasis.
- Explore the therapeutic potential of LTF in ccRCC.
- Elucidate the molecular mechanism of LTF in ccRCC progression.
Main Methods:
- Analysis of TCGA database for LTF expression in ccRCC tissues.
- In vitro experiments using ccRCC cell lines (A498, ACHN) to assess cell migration.
- Gene set enrichment analysis (GSEA) and RT-PCR to evaluate epithelial-mesenchymal transition (EMT).
- In vivo studies assessing lung metastasis in a mouse model.
- Investigating the interaction between LTF and LRP1.
Main Results:
- LTF is significantly downregulated in ccRCC tumors, particularly in metastatic cases.
- LTF overexpression suppresses ccRCC cell migration; LTF knockdown enhances it.
- LTF expression inversely correlates with EMT progression in ccRCC.
- Recombinant LTF protein inhibits cell migration and lung metastasis.
- LTF's inhibitory effect on migration is mediated through LRP1.
- Combined LTF downregulation and LRP1 upregulation predict poor patient survival.
Conclusions:
- LTF acts as a suppressor of ccRCC metastasis.
- LTF interacts with LRP1 to inhibit metastatic progression.
- Recombinant LTF protein is a potential therapeutic agent for metastatic ccRCC.
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