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3-D Cell Culture System for Studying Invasion and Evaluating Therapeutics in Bladder Cancer
Published on: September 13, 2018
Growth differentiation factor-9 expression is inversely correlated with an aggressive behaviour in human
1Metastasis and Angiogenesis Research Group, Cardiff University School of Medicine, Cardiff CF14 4XN, UK.
Abstract:
Growth differentiation factor-9 (GDF-9) is a family member of bone morphogenetic proteins (BMPs), which belong to the TGF-β superfamily. There has been a recent surge of interest in the role of growth differentiation factors and other BMPs in the development and spread of cancer. However, the role of GDF-9 in bladder cancer remains unknown. The present study investigated the expression of GDF-9 in normal and malignant human bladder tissue and its molecular interactions within bladder cancer cells. The expression of GDF-9 in human bladder tissues and bladder cancer cell lines was assessed at both the mRNA and protein levels using RT-PCR and immunohistochemistry, respectively. Full-length GDF-9 cDNA was amplified from normal mammary tissues. GDF-9 was overexpressed in bladder cancer cell lines using a mammalian expression construct. The effect of GDF-9 on cellular functions, was examined in bladder cancer cells overexpressing GDF-9 using a variety of in vitro assays. In normal bladder tissues, stronger staining of GDF-9 was seen in transitional cells, both in the cytoplasm and in the nucleus. In contrast, the staining of GDF-9 was notably weak or absent in cancer cells of tumour tissues. Similarly, the bladder cancer cell lines RT112 and EJ138, expressed very low levels of GDF-9. Moreover, overexpression of GDF-9 reduced the growth, adhesion and migration of bladder cell lines in vitro. However, the overexpression of GDF-9 had little bearing on the invasion of bladder cell lines in vitro. In conclusion, GDF-9 is expressed at lower levels in human bladder cancer cells compared with normal transitional cells of the bladder. GDF-9 levels are inversely correlated with the growth, adhesion and migration of bladder cancer cells in vitro. The results of the present study suggest that GDF-9 is a potential tumour suppressor in human bladder cancer.
Insights
Growth Differentiation Factor-9 (GDF-9) is downregulated in bladder cancer, with lower levels correlating to increased cancer cell growth, adhesion, and migration. These findings suggest GDF-9 acts as a tumor suppressor in bladder cancer.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Growth Differentiation Factor-9 (GDF-9) is a TGF-β superfamily member with roles in development.
- Recent interest focuses on growth differentiation factors and bone morphogenetic proteins (BMPs) in cancer progression.
- The specific role of GDF-9 in bladder cancer has not been previously established.
Purpose of the Study:
- To investigate GDF-9 expression in normal and malignant human bladder tissues.
- To examine the molecular interactions of GDF-9 within bladder cancer cells.
- To determine the functional impact of GDF-9 on bladder cancer cell behavior.
Main Methods:
- Assessed GDF-9 mRNA and protein expression using RT-PCR and immunohistochemistry.
- Amplified full-length GDF-9 cDNA from normal mammary tissues.
- Overexpressed GDF-9 in bladder cancer cell lines and performed in vitro functional assays.
Main Results:
- GDF-9 showed stronger expression in normal bladder transitional cells compared to bladder cancer tissues.
- Bladder cancer cell lines (RT112, EJ138) exhibited significantly lower GDF-9 levels.
- Overexpression of GDF-9 reduced bladder cancer cell growth, adhesion, and migration in vitro.
Conclusions:
- GDF-9 expression is downregulated in human bladder cancer.
- GDF-9 levels are inversely correlated with bladder cancer cell proliferation, adhesion, and migration.
- GDF-9 demonstrates potential as a tumor suppressor in human bladder cancer.
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