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Updated: Mar 10, 2026

Laser-capture Microdissection of Human Prostatic Epithelium for RNA Analysis
Published on: November 26, 2015
Long intragenic non-coding RNA lincRNA-p21 suppresses development of human prostate cancer
Xiaohai Wang1, Yuan Ruan1, Xingjie Wang1
1Department of Urology, Shanghai General Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Objectives:
Prostate cancer is one of the most frequent malignancies in men, worldwide, although its underlying mechanisms are not fully understood. Long non-coding RNAs participate in development of human cancers. In this invetsigation, we aimed to study the roles of lincRNA-p21 in development of human prostate cancer.
Materials And Methods:
Expression of lincRNA-p21 was assessed by real-time PCR in cell lines and in human tissues. Lentivirus carrying sh-lincRNA-p21, lincRNA-p21 or control constructs were used to determine their effects on cell proliferation and apoptosis. A mouse xenograft model was employed to explore the functions of lincRNA-p21 on cancer cell population growth in vivo. Relationships between p53 downstream genes and lincRNA-p21 levels were explored by real-time PCR, western blotting and chromatin immunoprecipitation.
Results:
LincRNA-p21 was found to be down-regulated in human prostate cancer, and low levels of lincRNA-p21 correlated with high disease stage and prediction of poor survival. We further showed that lincRNA-p21 inhibited prostate cancer cell proliferation and colony formation in vitro and reduced rate of prostate cancer cell population growth in vivo. Study of mechanisms involved revealed that lincRNA-p21 promoted apoptosis and induced expression of p53 downstream genes by regulating p53 binding to their promoters. Finally, we showed that expression of p53 downstream genes was reduced in the malignant prostate tissues, which correlated with lincRNA-p21 level.
Conclusions:
Our findings indicated that lincRNA-p21 inhibited development of human prostate cancer partly by regulating p53 downstream gene expression and partly by apoptotic activation.
Insights
Long non-coding RNA p21 (lincRNA-p21) is down-regulated in prostate cancer, inhibiting tumor growth and promoting apoptosis. Its regulation of p53 downstream genes suggests a tumor-suppressive role in prostate cancer development.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Prostate cancer is a leading malignancy in men globally, with complex underlying mechanisms.
- Long non-coding RNAs (lncRNAs) are increasingly recognized for their roles in human cancer development.
- The specific function of lincRNA-p21 in prostate cancer pathogenesis requires elucidation.
Purpose of the Study:
- To investigate the role of lincRNA-p21 in the development of human prostate cancer.
- To explore the molecular mechanisms by which lincRNA-p21 influences prostate cancer progression.
Main Methods:
- Real-time PCR was used to assess lincRNA-p21 expression in prostate cancer cell lines and tissues.
- Lentiviral vectors were employed to manipulate lincRNA-p21 levels, assessing effects on cell proliferation and apoptosis.
- In vivo studies utilized a mouse xenograft model to evaluate lincRNA-p21's impact on tumor growth.
- Western blotting and chromatin immunoprecipitation analyzed the relationship between lincRNA-p21 and p53 downstream genes.
Main Results:
- LincRNA-p21 was found to be down-regulated in human prostate cancer tissues, correlating with advanced disease stage and poor survival.
- Overexpression of lincRNA-p21 inhibited prostate cancer cell proliferation and colony formation in vitro and reduced tumor growth in vivo.
- LincRNA-p21 was shown to promote apoptosis and induce p53 downstream gene expression by regulating p53 binding to their promoters.
- Reduced expression of p53 downstream genes in malignant prostate tissues correlated with lower lincRNA-p21 levels.
Conclusions:
- LincRNA-p21 acts as a tumor suppressor in human prostate cancer.
- Its inhibitory effects are partly mediated through the regulation of p53 downstream gene expression.
- Apoptotic activation by lincRNA-p21 also contributes to its anti-cancer role in prostate cancer development.
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