Abstract

LHPP, a histidine phosphatase, has been implicated in tumour progression. However, its role, underlying mechanisms, and prognostic significance in human gastric cancer (GC) are elusive. Here, we obtained GC tissues and corresponding normal tissues from 48 patients and identified LHPP as a downregulated gene via RNA-seq. qRT-PCR and western blotting were applied to examine LHPP levels in normal and GC tissues. The prognostic value of LHPP was elucidated using tissue microarray and IHC analyses in two independent GC cohorts. The functional roles and mechanistic insights of LHPP in GC growth and metastasis were evaluated in vitro and in vivo. The results showed that LHPP expression was significantly decreased in GC tissues at both the mRNA and protein levels. Multivariate Cox regression analysis revealed that LHPP was an independent prognostic factor and effective predictor in patients with GC. The low expression of LHPP was significantly related to the poor prognosis and chemotherapy sensitivity of gastric cancer patients. Moreover, elevated LHPP expression effectively suppressed GC growth and metastasis in vitro and in vivo. Mechanistically, the m6A modification of LHPP mRNA by METTL14 represses its expression; LHPP inhibits the phosphorylation of GSK3b through acetylation and mediates HIF1A to inhibit glycolysis, proliferation, invasion and metastasis of gastric cancer cells. Together, our findings suggest that LHPP is regulated by m6A methylation and regulates the metabolism of GC by changing the acetylation level. Thus, LHPP is a potential predictive biomarker and therapeutic target for GC.

Details

Title
m6A methylation mediates LHPP acetylation as a tumour aerobic glycolysis suppressor to improve the prognosis of gastric cancer
Author
Jian-Xian, Lin 1 ; Ning-Zi, Lian 2 ; You-Xin, Gao 1 ; Qiao-Ling, Zheng 3 ; Ying-Hong, Yang 3 ; Yu-Bin, Ma 4 ; Zhi-Song, Xiu 5 ; Qing-Zhu, Qiu 1 ; Wang, Hua-Gen 1 ; Chao-Hui, Zheng 1 ; Li, Ping 1 ; Jian-Wei, Xie 1 ; Lu, Jun 1 ; Qi-Yue, Chen 1 ; Long-Long, Cao 1 ; Lin, Mi 1 ; Jia-Bin, Wang 1 ; Chang-Ming, Huang 1   VIAFID ORCID Logo 

 Fujian Medical University Union Hospital, Department of Gastric Surgery, Fuzhou, China (GRID:grid.411176.4) (ISNI:0000 0004 1758 0478); Fujian Medical University, Key Laboratory of Ministry of Education of Gastrointestinal Cancer, Fuzhou, China (GRID:grid.256112.3) (ISNI:0000 0004 1797 9307); Fujian Medical University, Fujian Key Laboratory of Tumor Microbiology, Fuzhou, China (GRID:grid.256112.3) (ISNI:0000 0004 1797 9307) 
 Fujian Medical University Union Hospital, Department of Gastric Surgery, Fuzhou, China (GRID:grid.411176.4) (ISNI:0000 0004 1758 0478); Fujian Medical University, Key Laboratory of Ministry of Education of Gastrointestinal Cancer, Fuzhou, China (GRID:grid.256112.3) (ISNI:0000 0004 1797 9307); Fujian Medical University, Fujian Key Laboratory of Tumor Microbiology, Fuzhou, China (GRID:grid.256112.3) (ISNI:0000 0004 1797 9307); Fujian Obstetrics and Gynecology Hospital, Department of Gynecology, Fuzhou, China (GRID:grid.256112.3) 
 Fujian Medical University Union Hospital, Department of Pathology, Fuzhou, China (GRID:grid.411176.4) (ISNI:0000 0004 1758 0478) 
 the Affiliated Hospital of Qinghai University, Department of Gastrointestinal Surgery, Xining, China (GRID:grid.459333.b) 
 Public Health School of Fujian Medical University, Fuzhou, China (GRID:grid.256112.3) (ISNI:0000 0004 1797 9307) 
Publication year
2022
Publication date
May 2022
Publisher
Springer Nature B.V.
e-ISSN
20414889
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2664212640
Copyright
© The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.