Lactate-induced up-regulation of PLEKHA4 promotes proliferation and apoptosis of human glioma cells.
10.12122/j.issn.1673-4254.2023.07.03
- Author:
Jingjing YE
1
;
Wenqin XU
1
;
Bangsheng XI
1
;
Nengqian WANG
1
;
Tianbing CHEN
1
Author Information
1. Key Laboratory of Non-coding RNA Transformation Research of Anhui Higher Education Institution, Wannan Medical College, Wuhu 241001, China.
- Publication Type:Journal Article
- Keywords:
PLEKHA4;
apoptosis;
biological function;
glioma;
lactate;
proliferation
- MeSH:
Humans;
Animals;
Mice;
Up-Regulation;
beta Catenin/metabolism*;
Mice, Nude;
Brain Neoplasms/pathology*;
Lactic Acid;
Cell Line, Tumor;
Glioma/pathology*;
Cell Proliferation;
Apoptosis;
Proto-Oncogene Proteins c-bcl-2/metabolism*;
RNA, Messenger/genetics*;
Gene Expression Regulation, Neoplastic
- From:
Journal of Southern Medical University
2023;43(7):1071-1080
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the effect of lactic acid-induced upregulation of PLEKHA4 expression on biological behaviors of glioma cells and the possible molecular mechanism.
METHODS:GEO database and GEPIA2 website were used to analyze the relationship between PLEKHA4 expression level and the pathological grade of glioma. A specific PLEKHA4 siRNA was transfected in glioma U251 and T98G cells, and the changes in cell proliferation ability were assessed by real-time cell analysis technology and Edu experiment. The colony-forming ability of the cells was evaluated using plate cloning assay, and cell cycle changes and cell apoptosis were analyzed with flow cytometry. The mRNA expression of PLEKHA4 was detected by PCR in glioma samples and controls and in glioma cells treated with lactic acid and glucose. Xenograft mice in vivo was used to detect tumor formation in nude mice; Western blotting was used to detect the expressions of cyclinD1, CDK2, Bcl2, β-catenin and phosphorylation of the key proteins in the MAPK signaling pathway.
RESULTS:The results of GEO database and online website analysis showed that PLEKHA4 was highly expressed in glioma tissues and was associated with poor prognosis; PLEKHA4 knockdown obviously inhibited the proliferation and attenuated the clone-forming ability of the glioma cells (P < 0.05). Flow cytometry showed that PLEKHA4 knockdown caused cell cycle arrest in G1 phase and promoted apoptosis of the cells (P < 0.01). PLEKHA4 gene mRNA expression was increased in glioma samples and glioma cells after lactate and glucose treatment (P < 0.01). PLEKHA4 knockdown, tumor formation ability of nude mice decreased; PLEKHA4 knockdown obviously lowered the expression of cyclinD1, CDK2, Bcl2 and other functional proteins, inhibited the phosphorylation of ERK and p38 and reduced the expression of β-catenin protein (P < 0.01).
CONCLUSION:PLEKHA4 knockdown inhibited the proliferation of glioma cells and promoted apoptosis by inhibiting the activation of the MAPK signaling pathway and expression of β-catenin. Lactic acid produced by glycolysis upregulates the expression of PLEKHA4 in glioma cells.
