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Updated: Jan 31, 2026

Molecular Profiling of the Invasive Tumor Microenvironment in a 3-Dimensional Model of Colorectal Cancer Cells and Ex vivo Fibroblasts
Published on: April 29, 2014
MiR-769 Inhibits Colorectal Cancer Cell Proliferation and Invasion by Targeting HEY1
Chao Han1, Yingming Song1, Changhong Lian1
1Department of General Surgery, Peace Hospital Affiliated to Changzhi Medical College, Changzhi, Shanxi, China (mainland).
Abstract:
BACKGROUND MicroRNAs (miRNAs) have been widely recognized as essential regulators in human cancers, including colorectal cancer (CRC). Whether miR-769 is implicated in CRC progression remains elusive. The present study aimed to determine the function of miR-769 in CRC. MATERIAL AND METHODS MiR-769 expression in CRC tissues and adjacent normal tissues were measured by quantitative real-time polymerase chain reaction (qRT-PCR) and in situ hybridization. Kaplan-Meier curve analysis was utilized to determine the association between miR-769 expression and prognosis in CRC patients. The effects of miR-769 overexpression on CRC cell proliferation, cell cycle and invasion were analyzed using Cell Counting Kit-8 (CCK8), fluorescence activated cell sorting (FACS), and Transwell assays. Western blot was utilized to assess the effect of miR-769 on HEY1 expression. RESULTS MiR-769 expression was decreased in CRC tissues. MiR-769 level was negatively correlated with the prognosis of CRC patients. Additionally, miR-769 overexpression remarkably inhibited cell proliferation, arrested CRC cells in G0 stage, and reduced cellular invasion. As to the mechanism, HEY1 was a direct target of miR-769; HEY1 level was inversely correlated with that of miR-769 in CRC tissues. Finally, overexpression of HEY1 reversed the effects of miR-769 on cell proliferation and invasion in CRC. CONCLUSIONS Our findings demonstrated that miR-769 suppressed the proliferation and invasion of CRC cells through targeting HEY1, which implied that miR-769 might be a novel therapeutic target for CRC treatment.
Insights
MicroRNA-769 (miR-769) acts as a tumor suppressor in colorectal cancer (CRC). Lower miR-769 levels correlate with poor prognosis, and its restoration inhibits CRC cell proliferation and invasion by targeting HEY1.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- MicroRNAs (miRNAs) are key regulators in human cancers, including colorectal cancer (CRC).
- The specific role of miR-769 in CRC progression was previously unclear.
- This study investigated the function of miR-769 in colorectal cancer.
Purpose of the Study:
- To determine the expression levels of miR-769 in CRC tissues.
- To analyze the correlation between miR-769 expression and patient prognosis.
- To elucidate the functional role and molecular mechanism of miR-769 in CRC.
Main Methods:
- Quantitative real-time polymerase chain reaction (qRT-PCR) and in situ hybridization for miR-769 expression.
- Kaplan-Meier analysis for prognosis.
- Cell Counting Kit-8 (CCK8), fluorescence activated cell sorting (FACS), and Transwell assays for cell proliferation, cell cycle, and invasion.
- Western blot to assess HEY1 expression.
Main Results:
- miR-769 expression was significantly decreased in CRC tissues compared to normal tissues.
- Lower miR-769 levels were negatively correlated with poorer patient prognosis.
- Overexpression of miR-769 inhibited CRC cell proliferation and invasion, and induced G0 cell cycle arrest.
- HEY1 was identified as a direct target of miR-769, with inverse expression correlation in CRC tissues.
- HEY1 overexpression counteracted the inhibitory effects of miR-769 on CRC cell proliferation and invasion.
Conclusions:
- miR-769 functions as a tumor suppressor in colorectal cancer.
- It inhibits CRC cell proliferation and invasion by directly targeting HEY1.
- miR-769 represents a potential novel therapeutic target for colorectal cancer treatment.
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