Related Experiment Video
Updated: Oct 7, 2025

Integration of Bioinformatics Approaches and Experimental Validations to Understand the Role of Notch Signaling in Ovarian Cancer
Published on: January 12, 2020
LncRNA HCG11 represses ovarian cancer cell growth via AKT signaling pathway
Xiaoping Chen1, Yusheng Yang2, Jie Sun3
1Department of Gynecology and Obstetrics, Ningbo Yinzhou Second Hospital, Ningbo, Zhejiang, China.
Aim:
Ovarian cancer is a main contributor of cancer-relevant deaths among women worldwide due to high incidence and mortality. Mounting evidence has unveiled that lncRNAs play critical roles in malignancies, including ovarian cancer. Although the tumor suppressor function of HCG11 in prostate cancer and glioma has been proved, investigations on HCG11 role in ovarian cancer are still scarce.
Methods:
Gene or protein expression was quantified by RT-qPCR or western blot. HCG11 effects on ovarian cancer were assessed by functional assays. Bioinformatics analysis and mechanism experiments were implemented to identify the association among HCG11, miR-1270, and PTEN.
Results:
HCG11 was weakly expressed in ovarian cancer and functioned as a tumor suppressor in ovarian cancer by retarding cell proliferation, migration, and EMT. Besides, HCG11 could bind to miR-1270 and PTEN was a target gene of miR-1270. Mechanically, HCG11 competitively bound with miR-1270 to upregulate PTEN. From rescue experiments, HCG11 impeded AKT/mTOR pathway to retard ovarian cancer cell growth by miR-1270/PTEN.
Conclusions:
HCG11 was a tumor suppressor in ovarian cancer cells and additionally, HCG11 regulated AKT/mTOR pathway to hinder ovarian cancer cell growth via modulating miR-1270/PTEN, indicating that HCG11 may represent a promising target for effective treatment of ovarian cancer patients.
Insights
HCG11 acts as a tumor suppressor in ovarian cancer, inhibiting cell growth and migration. This long non-coding RNA targets miR-1270 to upregulate PTEN, ultimately hindering the AKT/mTOR pathway for potential ovarian cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Ovarian cancer is a leading cause of cancer deaths in women globally.
- Long non-coding RNAs (lncRNAs) are increasingly recognized for their roles in cancer development.
- The tumor suppressor role of HCG11 is established in other cancers, but its function in ovarian cancer remains under-investigated.
Purpose of the Study:
- To investigate the role of HCG11 in ovarian cancer.
- To elucidate the molecular mechanism by which HCG11 affects ovarian cancer progression.
- To explore the potential of HCG11 as a therapeutic target for ovarian cancer.
Main Methods:
- Gene and protein expression analysis using RT-qPCR and western blot.
- Functional assays to assess the impact of HCG11 on ovarian cancer cell behavior (proliferation, migration, EMT).
- Bioinformatics and mechanistic experiments to determine the interaction between HCG11, miR-1270, and PTEN, and its effect on the AKT/mTOR pathway.
Main Results:
- HCG11 expression is reduced in ovarian cancer tissues.
- HCG11 functions as a tumor suppressor by inhibiting cell proliferation, migration, and epithelial-mesenchymal transition (EMT).
- HCG11 directly binds to miR-1270, and PTEN is a target of miR-1270. HCG11 upregulates PTEN by competitively binding to miR-1270, thereby inhibiting the AKT/mTOR pathway and retarding ovarian cancer cell growth.
Conclusions:
- HCG11 acts as a tumor suppressor in ovarian cancer.
- HCG11 exerts its tumor-suppressive effects by modulating the miR-1270/PTEN axis, leading to the inhibition of the AKT/mTOR pathway.
- HCG11 represents a potential therapeutic target for ovarian cancer treatment.
Related Concept Videos
lncRNA - Long Non-coding RNAs
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Inhibition of Cdk Activity
Cancer-Critical Genes II: Tumor Suppressor Genes
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
The Retinoblastoma Gene
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
PI3K/mTOR/AKT Signaling Pathway
