Related Experiment Video
Updated: Dec 30, 2025

Describing a Transcription Factor Dependent Regulation of the MicroRNA Transcriptome
Published on: June 15, 2016
CAT104 silence behaves as a tumor suppressor in human leukemia cells by down regulating miR-182 expression
Chengfang Zhang1, Guanli Song2, Guanbo Song3
1Department of Clinical Laboratory, Jining No. 1 People's Hospital Jining 272011, Shandong, China.
Background:
LncRNAs and miRNAs are found to play crucial roles in the tumorigenesis of acute myeloid leukemia (AML). We aimed to investigate the functions and mechanisms of lncRNA-CAT104 and miR-182 in AML.
Methods:
Expression of CAT104, miR-182, and ZEB1 in K562 and HL60 cell lines was respectively or synchronously altered by transfection. Expressions of CAT104, miR-182 and ZEB1 in cell were then analyzed by qRT-PCR. Cell viability, migration, invasion and apoptosis were evaluated by MTT, transwell assays and flow cytometry, respectively. Protein expressions of ZEB1 and factors related with apoptosis and two signal pathways (Wnt/β-catenin and JNK) were detected by western blot.
Results:
CAT104 expressed highly in K562 and HL60 cells compared to embryonic kidney cell line HEK293 (P < 0.001). Knockdown of CAT104 inhibited cell viability, migration and invasion, but increased cell apoptosis of K562 and HL60 cells through inhibitionof miR-182 (P < 0.05). miR-182 promoted cell survival, migration and invasion through upregulatingthe expression of ZEB1 (P < 0.05). miR-182 silence deactivated Wnt/β-catenin and JNK signal pathways by downregulating the expression of ZEB1 in K562 and HL60 cells.
Conclusion:
LncRNA-CAT104 expressed highly in leukemia cells and its silence inhibited cell survival, migration and invasion by downregulating miR-182 expression. miR-182 functioned as an oncogene by upregulating ZEB1 via which miR-182 silence deactivated Wnt/β-catenin and JNK signal pathways in leukemia cells.
Insights
Long non-coding RNA CAT104 and microRNA 182 are key players in acute myeloid leukemia (AML) tumorigenesis. Silencing CAT104 inhibits AML cell growth and metastasis by downregulating miR-182, which acts as an oncogene by upregulating ZEB1.
Area of Science:
- Molecular Biology
- Cancer Research
- Genetics
Background:
- Long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) are implicated in acute myeloid leukemia (AML) development.
- Investigating the roles of lncRNA-CAT104 and miR-182 in AML pathogenesis is crucial.
Purpose of the Study:
- To elucidate the functions and underlying mechanisms of lncRNA-CAT104 and miR-182 in AML.
- To determine the relationship between CAT104, miR-182, and ZEB1 in leukemia cells.
Main Methods:
- Quantitative reverse transcription polymerase chain reaction (qRT-PCR) to analyze gene expression.
- Cell viability, migration, invasion, and apoptosis assays (MTT, transwell, flow cytometry).
- Western blotting to assess protein expression and signaling pathways (Wnt/β-catenin, JNK).
Main Results:
- CAT104 was highly expressed in AML cell lines (K562, HL60).
- CAT104 knockdown suppressed cell viability, migration, and invasion while increasing apoptosis, mediated by miR-182 inhibition.
- miR-182 promoted cell survival, migration, and invasion by upregulating ZEB1, subsequently deactivating Wnt/β-catenin and JNK pathways.
Conclusions:
- lncRNA-CAT104 is upregulated in leukemia cells and its suppression inhibits cell survival and metastasis via miR-182 downregulation.
- miR-182 acts as an oncogene in AML by enhancing ZEB1 expression, leading to the deactivation of Wnt/β-catenin and JNK signaling pathways.
Related Concept Videos
MicroRNAs
MicroRNAs
Abnormal Proliferation
Loss of Tumor Suppressor Gene Functions
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
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,...

