Evidence map›Paper›PMID 41857481›Full record

ArticleCNS neuroscience & therapeutics2026

The PKA/MBD2 Axis Transcriptionally Represses INPP5A to Modulate PI3K/Akt Signaling and Accelerate Pituitary Tumorigenesis.

Qian Jiang, Yaorui Wang, Zihan Wang, Quanji Wang, Sihan Li, Linpeng Xu, Zhuo Zhang, Zhoubin Tan, Huaqiu Zhang, Kai Shu and 3 more

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Qian JiangDepartment of Neurosurgery, Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei province, China.ORCID 0009-0001-0298-6542
Yaorui WangDepartment of Neurosurgery, Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei province, China.ORCID 0009-0009-0312-204X
Zihan WangDepartment of Neurosurgery, Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei province, China.
Quanji WangDepartment of Neurosurgery, Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei province, China.
Sihan LiDepartment of Neurosurgery, Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei province, China.
Linpeng XuDepartment of Neurosurgery, Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei province, China.
Zhuo ZhangDepartment of Neurosurgery, Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei province, China.
Zhoubin TanDepartment of Neurosurgery, Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei province, China.
Huaqiu ZhangDepartment of Neurosurgery, Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei province, China.
Kai ShuDepartment of Neurosurgery, Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei province, China.
Ting LeiDepartment of Neurosurgery, Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei province, China.
Yimin HuangDepartment of Neurosurgery, Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei province, China.
Zhuowei LeiSino-German Neuro-Oncology Molecular Laboratory, Department of Neurosurgery, Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.

Funding

National Natural Science Foundation of China 82173136National Natural Science Foundation of China 82573287
6 · The paper itself

Abstract

CONTEXT AND

objectiveThe malignant progression of pituitary neuroendocrine tumors (PitNETs) is closely associated with abnormalities in the phosphoinositide signaling pathway. This study aims to investigate the regulatory role and molecular mechanism of inositol polyphosphate 5-phosphatase A (INPP5A) in the malignant progression of PitNETs, with a focus on its interaction with the PI3K/Akt signaling pathway and the epigenetic regulator MBD2.

settingTongji Hospital of Tongji medical college of Huazhong University of Science and Technology.

designAnalyze genes related to IP3 metabolism in single-cell sequencing samples of PitNETs from NCBI, and perform immunofluorescence staining and statistical analysis on samples from 62 patients with PitNETs.

resultINPP5A was significantly downregulated in PitNETs, and its expression was negatively correlated with tumor invasiveness, Ki67 index, and volume, Overexpression of INPP5A inhibited tumor cell proliferation, migration, and hormone secretion, while knockdown of INPP5A promoted these malignant phenotypes, INPP5A negatively regulated the PI3K/Akt pathway by degrading IP3, MBD2 directly bound to the INPP5A promoter region to mediate transcriptional repression, Activation of PKA signaling phosphorylated MBD2 (at S99), recruited 14-3-3σ to stabilize the MBD2 protein, and enhanced the inhibition of INPP5A.

conclusionINPP5A acts as a tumor suppressor gene in PitNETs, and its downregulation promotes tumor malignant progression by activating the PI3K/Akt pathway. MBD2 and its PKA-mediated phosphorylation are key mechanisms for INPP5A transcriptional repression. Targeting the MBD2-INPP5A-PI3K/Akt axis may provide a new strategy for the treatment of PitNETs.

Indexed as

CarcinogenesisCyclic AMP-Dependent Protein KinasesDNA-Binding ProteinsInositol Polyphosphate 5-PhosphatasesNeuroendocrine TumorsPhosphatidylinositol 3-KinasesPhosphoric Monoester HydrolasesPituitary NeoplasmsProto-Oncogene Proteins c-aktAnimalsCell Line, TumorGene Expression Regulation, NeoplasticHumansSignal TransductionCyclic AMP-Dependent Protein KinasesDNA-Binding ProteinsInositol Polyphosphate 5-PhosphatasesPhosphatidylinositol 3-KinasesPhosphoric Monoester HydrolasesProto-Oncogene Proteins c-akt14–3‐3σINPP5AMBD2PitNETPKA

Identifiers

PMID41857481
PMCPMC13093853

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.