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Updated: Jan 30, 2026

Modeling Oral-Esophageal Squamous Cell Carcinoma in 3D Organoids
Published on: December 23, 2022
MicroRNA-145 performs as a tumor suppressor in human esophageal squamous cell carcinoma by targeting phospholipase C
Chun Tang1,2, Jin-Yuan He3, Chao Yu4
1Department of Nephrology, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, P.R. China.
Abstract:
Esophageal squamous cell carcinoma (ESCC) is the leading pathologic type in China. miR-145 has been reported to be downregulated in multiple tumors. This study was aimed to investigate the role of miR-145 in ESCC. miR-145 expression was investigated in 65 ESCC samples as well as four ESCC cell lines by quantitative real-time polymerase chain reaction (qRT-PCR). Targetscan 6.2 website (http://www.targetscan.org/) was used to predict the targets of miR-145. Expression of phospholipase C epsilon 1 (PLCE1) messenger RNA and protein was detected by qRT-PCR or Western blot. MTT and wound healing assay were conducted to explore the effects of miR-145 on the proliferation and migration of ESCC cell lines, respectively. miR-145 was significantly decreased in ESCC tissues. An inverse correlation between miR-145 and invasion depth and TNM stage were observed. PLCE1 was a direct target of miR-145, and the expression of PLCE1 was inversely correlated with miR-145 expression in ESCC tissues. In addition, overexpression of miR-145 suppressed cell proliferation and migration in ESCC cells. The enforced expression of PLCE1 partially reversed the suppressive effect of miR-145. These results prove that miR-145 may perform as a tumor suppressor in ESCC by targeting PLCE1.
Insights
MicroRNA-145 (miR-145) is downregulated in esophageal squamous cell carcinoma (ESCC). Restoring miR-145 suppresses ESCC cell proliferation and migration by targeting PLCE1, indicating its tumor suppressor role.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Esophageal squamous cell carcinoma (ESCC) is a prevalent cancer in China.
- MicroRNA-145 (miR-145) is frequently downregulated in various cancers, suggesting a potential role in tumorigenesis.
Purpose of the Study:
- To investigate the expression and function of miR-145 in ESCC.
- To identify the molecular targets of miR-145 in ESCC.
- To elucidate the therapeutic potential of miR-145 in ESCC.
Main Methods:
- Quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot were used to assess miR-145 and PLCE1 expression.
- Bioinformatic tools predicted miR-145 targets.
- MTT and wound healing assays evaluated the effects of miR-145 on ESCC cell proliferation and migration.
Main Results:
- miR-145 expression was significantly decreased in ESCC tissues and inversely correlated with invasion depth and TNM stage.
- Phospholipase C epsilon 1 (PLCE1) was identified as a direct target of miR-145, with inverse expression correlation observed in ESCC tissues.
- Overexpression of miR-145 inhibited ESCC cell proliferation and migration, an effect partially reversed by PLCE1 re-expression.
Conclusions:
- miR-145 functions as a tumor suppressor in ESCC.
- Targeting PLCE1 is a key mechanism through which miR-145 exerts its tumor-suppressive effects in ESCC.
- miR-145 represents a potential therapeutic target for esophageal squamous cell carcinoma.
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