Related Experiment Video
Updated: Mar 27, 2026

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Onco-miR-24 regulates cell growth and apoptosis by targeting BCL2L11 in gastric cancer
Haiyang Zhang1, Jingjing Duan1, Yanjun Qu1
1Tianjin Medical University Cancer Institute and Hospital, Key Laboratory of Cancer Prevention and Therapy, National Clinical Research Center for Cancer, Tianjin, 300060, China.
Abstract:
Gastric cancer is one of the most common malignancies worldwide; however, the molecular mechanism in tumorigenesis still needs exploration. BCL2L11 belongs to the BCL-2 family, and acts as a central regulator of the intrinsic apoptotic cascade and mediates cell apoptosis. Although miRNAs have been reported to be involved in each stage of cancer development, the role of miR-24 in GC has not been reported yet. In the present study, miR-24 was found to be up-regulated while the expression of BCL2L11 was inhibited in tumor tissues of GC. Studies from both in vitro and in vivo shown that miR-24 regulates BCL2L11 expression by directly binding with 3'UTR of mRNA, thus promoting cell growth, migration while inhibiting cell apoptosis. Therefore, miR-24 is a novel onco-miRNA that can be potential drug targets for future clinical use.
Insights
MicroRNA-24 (miR-24) promotes gastric cancer (GC) growth by inhibiting the apoptosis regulator BCL2L11. This finding identifies miR-24 as a potential therapeutic target for gastric cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Gastric cancer (GC) is a prevalent malignancy with incompletely understood molecular mechanisms.
- BCL2L11, a member of the BCL-2 family, is crucial in regulating apoptosis.
- MicroRNAs (miRNAs) play significant roles in cancer development, but miR-24's function in GC remains uncharacterized.
Purpose of the Study:
- To investigate the role of miR-24 in gastric cancer.
- To elucidate the molecular mechanism by which miR-24 influences gastric cancer progression.
- To assess the potential of miR-24 as a therapeutic target in gastric cancer.
Main Methods:
- Quantitative real-time PCR to measure miR-24 and BCL2L11 expression in GC tissues.
- In vitro cell culture experiments assessing cell growth, migration, and apoptosis.
- In vivo studies to validate the findings.
- Luciferase reporter assays to confirm direct binding of miR-24 to BCL2L11 mRNA.
Main Results:
- miR-24 was significantly upregulated in gastric cancer tissues.
- BCL2L11 expression was inversely correlated with miR-24 levels in GC tissues.
- Overexpression of miR-24 promoted gastric cancer cell proliferation and migration while inhibiting apoptosis.
- miR-24 directly targets BCL2L11 mRNA, leading to its downregulation.
Conclusions:
- miR-24 acts as an oncogenic miRNA in gastric cancer by suppressing BCL2L11.
- miR-24 promotes tumor growth and metastasis in gastric cancer.
- miR-24 represents a promising novel therapeutic target for gastric cancer intervention.
Related Concept Videos
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
mTOR Signaling and Cancer Progression
The Intrinsic Apoptotic Pathway
Abnormal Proliferation
Mitogens and the Cell Cycle
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,...
