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Updated: Apr 8, 2026

Genome-Wide Analysis of DNA Methylation in Gastrointestinal Cancer
Published on: September 18, 2020
PABPC1 exerts carcinogenesis in gastric carcinoma by targeting miR-34c
Jie Zhu1, Hao Ding1, Xiaohong Wang1
1Department of General Surgery, Huadong Hospital Shanghai 200040.
Abstract:
As one of the common malignant tumors that threaten human health severely, gastric carcinoma is the second highest cause of cancer death and the fourth most common cancer globally. However, the mechanism underlying gastric cancer is still not fully understood. PABPC1 plays an important role in translation, control the rate of mRNA deadenylation and participates in mRNA decay, which is involved in carcinogenesis. Here in present study, we reported that PABPC1 is an oncogenic protein in gastric carcinoma. The results showed that PABPC1 is upregulated in gastric carcinoma tissues, and high PABPC1 expression predicts poor survival. PABPC1 regulates proliferation and transformation of gastric cancer cells in vitro and in vivo. PABPC1 knockdown induces apoptosis by upregulating pro-apoptotic proteins and downregulating anti-apoptotic proteins. In addition, miR-34c is a target of PABPC1, and miR-34c is critically essential for the function of PABPC1. In summary, PABPC1 exerts carcinogenesis and promotes growth and survival of gastric cancer cells by regulating miR-34c.
Insights
Poly(A)-binding protein 1 (PABPC1) acts as an oncogene in gastric cancer, promoting tumor growth and survival. Its upregulation in gastric carcinoma tissues correlates with poor patient prognosis and is linked to miR-34c regulation.
Area of Science:
- Molecular Oncology
- Gastrointestinal Cancer Research
Background:
- Gastric carcinoma is a leading cause of cancer death globally, with its underlying mechanisms incompletely understood.
- Poly(A)-binding protein 1 (PABPC1) is crucial for mRNA processing, including translation and decay, and has been implicated in carcinogenesis.
Purpose of the Study:
- To investigate the role of PABPC1 as an oncogenic protein in gastric carcinoma.
- To elucidate the functional mechanisms by which PABPC1 influences gastric cancer progression and survival.
Main Methods:
- Analysis of PABPC1 expression levels in gastric carcinoma tissues.
- In vitro and in vivo studies to assess the impact of PABPC1 on cell proliferation, transformation, and apoptosis.
- Investigation of the regulatory relationship between PABPC1 and microRNA-34c (miR-34c).
Main Results:
- PABPC1 expression is significantly upregulated in gastric carcinoma tissues.
- High PABPC1 expression is associated with poor patient survival.
- PABPC1 knockdown inhibits gastric cancer cell proliferation and transformation, and induces apoptosis by modulating pro- and anti-apoptotic proteins.
- PABPC1 directly targets and regulates miR-34c, which is essential for PABPC1's oncogenic functions.
Conclusions:
- PABPC1 functions as an oncogenic protein in gastric carcinoma.
- PABPC1 promotes gastric cancer cell growth and survival, partly through its regulation of miR-34c.
- Targeting PABPC1 may represent a therapeutic strategy for gastric cancer.
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