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Long non-coding RNA SNHG20 promotes non-small cell lung cancer cell proliferation and migration by epigenetically
Zhenyao Chen1, Xin Chen1, Ping Chen1,2
1Department of Oncology, Second Affiliated Hospital, Nanjing Medical University, Nanjing, People's Republic of China.
Abstract:
Mounting evidence demonstrates that long non-coding RNAs (lncRNAs) are novel transcripts governing multiple biological processes, and their dysregulation is involved in the development and progression of multiple types of cancers. Small Nucleolar RNA Host Gene 20 (SNHG20) is a 2183 bp lncRNA, and its overexpression predicts poor prognosis in colorectal cancer and hepatocellular carcinoma. However, the clinical relevance of SNHG20 and its molecular mechanisms affecting cancer cell phenotype have not been documented. Here, we found that SNHG20 was upregulated in non-small cell lung cancer (NSCLC) tissues compared with normal samples. Higher SNHG20 expression was significantly associated with advanced tumor, lymph node and metastases (TNM) stage and tumor size, as well as poorer overall survival. Moreover, knockdown of SNHG20 repressed NSCLC cell proliferation, migration and induced cell apoptosis. Mechanistic investigations revealed that SNHG20 could interact with EZH2 (enhancer of zeste homolog 2), thereby repressing P21 expression. Furthermore, rescue experiments indicated that SNHG20 functioned as an oncogene partly via repressing p21 in NSCLC cells. Taken together, our findings demonstrate that SNHG20 is a new candidate for use in NSCLC diagnosis, prognosis and therapy.
Insights
Small Nucleolar RNA Host Gene 20 (SNHG20) is upregulated in non-small cell lung cancer (NSCLC). This long non-coding RNA promotes cancer progression by interacting with EZH2 and repressing p21, suggesting its potential as a diagnostic and therapeutic target.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Long non-coding RNAs (lncRNAs) regulate biological processes, and their dysregulation is implicated in cancer.
- Small Nucleolar RNA Host Gene 20 (SNHG20) overexpression is linked to poor prognosis in colorectal and hepatocellular carcinomas.
- The clinical significance and molecular mechanisms of SNHG20 in non-small cell lung cancer (NSCLC) remain largely undocumented.
Purpose of the Study:
- To investigate the clinical relevance and molecular mechanisms of SNHG20 in non-small cell lung cancer (NSCLC).
- To determine the association between SNHG20 expression and clinicopathological features and prognosis in NSCLC patients.
Main Methods:
- Quantitative real-time PCR to measure SNHG20 expression in NSCLC tissues and adjacent normal samples.
- Western blotting and cell-based assays (proliferation, migration, apoptosis) to assess the functional role of SNHG20.
- RNA immunoprecipitation and Western blotting to investigate the interaction between SNHG20, EZH2, and p21.
Main Results:
- SNHG20 was significantly upregulated in NSCLC tissues compared to normal tissues.
- Higher SNHG20 expression correlated with advanced TNM stage, larger tumor size, and poorer overall survival.
- Knockdown of SNHG20 inhibited NSCLC cell proliferation and migration while inducing apoptosis.
- SNHG20 directly interacted with EZH2 to suppress p21 expression, functioning as an oncogene in NSCLC.
Conclusions:
- SNHG20 is upregulated in NSCLC and associated with adverse clinical outcomes.
- SNHG20 promotes NSCLC progression by interacting with EZH2 and repressing p21.
- SNHG20 represents a potential biomarker for NSCLC diagnosis and prognosis, and a therapeutic target.
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