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Updated: Oct 20, 2025

Author Spotlight: RNA FISH for Locating lncRNA-SNHG6 in Osteosarcoma Cells
Published on: June 16, 2023
lncRNA HCG11 suppresses human osteosarcoma growth through upregulating p27 Kip1
Jie Gu1, Bo Dai1, Xuchao Shi1
1Department of Orthopaedics Surgery, Beilun People's Hospital, Ningbo, Zhejiang, China.
Abstract:
Osteosarcoma (OS) is a common malignant bone cancer threatening children and young adults. Emerging evidence indicates that long non-coding RNAs (lncRNAs) play crucial roles in the progression of OS. Herein, we want to clarify the roles of lncRNA human leukocyte antigen complex group 11 (HCG11) in OS. Our data revealed that HCG11 expression is decreased in OS, which is a result of transcriptional repression of YY1. Low HCG11 level is closely associated with larger tumor size and shorter overall survival of OS patients. HCG11 negatively regulates cell proliferation, cell cycle, DNA replication in vitro and tumor growth in vivo. HCG11 can raise p27 Kip1 expression via binding to miR-942-5p and IGF2BP2, and p27 Kip1 acts as a key effector for HCG11 exerting biological functions. In conclusion, HCG11 is downregulated in OS, and restrains OS growth both in vitro and in vivo by raising p27 Kip1 expression via binding to miR-942-5p and IGF2BP2.
Insights
Long non-coding RNA HCG11 is downregulated in osteosarcoma (OS), a bone cancer. Restoring HCG11 restrains OS growth by increasing p27 Kip1 expression, offering a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Osteosarcoma (OS) is a prevalent bone cancer in pediatric and young adult populations.
- Long non-coding RNAs (lncRNAs) are increasingly recognized for their significant roles in OS progression.
Purpose of the Study:
- To investigate the functional role of lncRNA human leukocyte antigen complex group 11 (HCG11) in osteosarcoma.
- To elucidate the molecular mechanisms underlying HCG11's function in OS.
Main Methods:
- Quantitative real-time PCR to assess HCG11 expression levels in OS tissues and cell lines.
- In vitro assays (proliferation, cell cycle, DNA replication) and in vivo tumor xenograft models to evaluate HCG11's biological functions.
- Mechanism studies involving RNA immunoprecipitation and Western blotting to confirm interactions between HCG11, miR-942-5p, IGF2BP2, and p27 Kip1.
Main Results:
- HCG11 expression was significantly decreased in OS tissues compared to normal tissues, correlated with tumor size and patient survival.
- Overexpression of HCG11 inhibited OS cell proliferation, cell cycle progression, and DNA replication in vitro, and suppressed tumor growth in vivo.
- HCG11 was found to upregulate p27 Kip1 expression by sponging miR-942-5p and interacting with IGF2BP2, with p27 Kip1 mediating HCG11's tumor-suppressive effects.
Conclusions:
- HCG11 is downregulated in osteosarcoma, acting as a tumor suppressor.
- HCG11 inhibits OS progression by enhancing p27 Kip1 expression through the miR-942-5p/IGF2BP2 axis.
- HCG11 represents a potential therapeutic target for osteosarcoma treatment.
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