Related Experiment Video
Updated: Jan 5, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Star-PAP regulates tumor protein D52 through modulating miR-449a/34a in breast cancer
Aizhu Duan1,2, Lingmei Kong1, Tao An1
1State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, P.R. China.
Abstract:
Tumor protein D52 (TPD52) is an oncogene amplified and overexpressed in various cancers. Tumor-suppressive microRNA-449a and microRNA-34a (miR-449a/34a) were recently reported to inhibit breast cancer cell migration and invasion via targeting TPD52. However, the upstream events are not clearly defined. Star-PAP is a non-canonical poly (A) polymerase which could regulate the expression of many miRNAs and mRNAs, but its biological functions are not well elucidated. The present study aimed to explore the regulative roles of Star-PAP in miR-449a/34a and TPD52 expression in breast cancer. We observed a negative correlation between the expression of TPD52 and Star-PAP in breast cancer. Overexpression of Star-PAP inhibited TPD52 expression, while endogenous Star-PAP knockdown led to increased TPD52. Furthermore, RNA immunoprecipitation assay suggested that Star-PAP could not bind to TPD52, independent of the 3'-end processing. RNA pull-down assay showed that Star-PAP could bind to 3'region of miR-449a. In line with these results, blunted cell proliferation or cell apoptosis caused by Star-PAP was rescued by overexpression of TPD52 or downregulation of miR-449a/34a. Our findings identified that Star-PAP regulates TPD52 by modulating miR-449a/34a, which may be an important molecular mechanism underlying the tumorigenesis of breast cancer and provide a rational therapeutic target for breast cancer treatment.
Insights
Star-PAP, a poly (A) polymerase, inhibits breast cancer progression by downregulating tumor protein D52 (TPD52) through microRNA-449a/34a (miR-449a/34a). This identifies Star-PAP as a potential therapeutic target for breast cancer.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- Tumor protein D52 (TPD52) is an oncogene implicated in various cancers.
- MicroRNA-449a and microRNA-34a (miR-449a/34a) are tumor suppressors targeting TPD52 in breast cancer.
- The upstream regulators of miR-449a/34a and TPD52 in breast cancer remain unclear.
Purpose of the Study:
- To investigate the role of Star-papillary (Star-PAP) in regulating miR-449a/34a and TPD52 expression in breast cancer.
- To elucidate the molecular mechanism by which Star-PAP influences breast cancer tumorigenesis.
Main Methods:
- Correlation analysis of TPD52 and Star-PAP expression in breast cancer.
- Overexpression and knockdown studies of Star-PAP.
- RNA immunoprecipitation and pull-down assays to determine molecular interactions.
- Rescue experiments involving TPD52 and miR-449a/34a modulation.
Main Results:
- A negative correlation was observed between TPD52 and Star-PAP expression.
- Star-PAP overexpression decreased TPD52 levels, while Star-PAP knockdown increased them.
- Star-PAP directly binds to the 3' region of miR-449a, independent of TPD52.
- Modulation of Star-PAP, miR-449a/34a, and TPD52 affected cell proliferation and apoptosis.
Conclusions:
- Star-PAP acts as a tumor suppressor in breast cancer by negatively regulating TPD52 expression via miR-449a/34a.
- This pathway represents a novel molecular mechanism in breast cancer development.
- Star-PAP emerges as a potential therapeutic target for breast cancer treatment.
Related Concept Videos
Abnormal Proliferation
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
MicroRNAs
MicroRNAs
Targeted Cancer Therapies
There are several types of targeted therapies against...
PI3K/mTOR/AKT Signaling Pathway

