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Induction of Invasive Transitional Cell Bladder Carcinoma in Immune Intact Human MUC1 Transgenic Mice: A Model for Immunotherapy Development
Published on: October 30, 2013
lncRNA-mediated ceRNA network in bladder cancer
Kun Li1, Tongyue Yao2, Ziqiang Wang1,2
1Department of Nuclear Medicine, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, 250014, China.
Abstract:
Bladder cancer is a common disease associated with high rates of morbidity and mortality. Although immunotherapy approaches such as adoptive T-cell therapy and immune checkpoint blockade have been investigated for the treatment of bladder cancer, their off-target effects and ability to affect only single targets have led to clinical outcomes that are far from satisfactory. Therefore, it is important to identify novel targets that can effectively control tumor growth and metastasis. It is well known that long noncoding RNAs (lncRNAs) are powerful regulators of gene expression. Increasing evidence has shown that dysregulated lncRNAs in bladder cancer are involved in cancer cell proliferation, migration, invasion, apoptosis, and epithelial-mesenchymal transition (EMT). In this review, we focus on the roles and underlying mechanisms of lncRNA-mediated competing endogenous RNA (ceRNA) networks in the regulation of bladder cancer progression. In addition, we discuss the potential of targeting lncRNA-mediated ceRNA networks to overcome cancer treatment resistance and its association with clinicopathological features and outcomes in bladder cancer patients. We hope this review will stimulate research to develop more effective therapeutic approaches for bladder cancer treatment.
Insights
Long noncoding RNAs (lncRNAs) regulate gene expression and are implicated in bladder cancer progression. Targeting lncRNA networks offers a promising strategy to overcome treatment resistance and improve patient outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Bladder cancer presents significant morbidity and mortality.
- Current immunotherapies like T-cell therapy and immune checkpoint blockade show limitations due to off-target effects and single-target specificity.
- Novel therapeutic targets are crucial for effective control of bladder cancer growth and metastasis.
Purpose of the Study:
- To review the roles and mechanisms of long noncoding RNA (lncRNA)-mediated competing endogenous RNA (ceRNA) networks in bladder cancer progression.
- To discuss the potential of targeting lncRNA-mediated ceRNA networks for overcoming cancer treatment resistance.
- To explore the association between lncRNA-mediated ceRNA networks, clinicopathological features, and patient outcomes in bladder cancer.
Main Methods:
- Literature review focusing on lncRNAs and ceRNA networks in bladder cancer.
- Analysis of existing evidence on the regulatory functions of lncRNAs in cancer cell proliferation, migration, invasion, apoptosis, and epithelial-mesenchymal transition (EMT).
- Discussion of therapeutic strategies targeting lncRNA-mediated ceRNA networks.
Main Results:
- Dysregulated lncRNAs are involved in key processes of bladder cancer progression, including proliferation, migration, invasion, apoptosis, and EMT.
- lncRNA-mediated ceRNA networks play a significant role in regulating gene expression within bladder cancer cells.
- Targeting these networks shows potential for overcoming resistance to existing cancer treatments.
Conclusions:
- lncRNAs are critical regulators in bladder cancer, influencing various aspects of tumor progression.
- lncRNA-mediated ceRNA networks represent a promising avenue for developing novel therapeutic strategies against bladder cancer.
- Further research into these networks could lead to improved treatment approaches and better patient outcomes.
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