Evidence map›Paper›PMID 40722111›Full record

ReviewCell & bioscience2025

Advances in research on SATB2 and its role in tumor development.

Ge Cheng, Chi Tian, Waner Wang, Yangyang Zhou, Xiaoqing Wang, Lei Zhang

Abstract readReview
In one paragraph

Review in Cell & bioscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Ge Cheng *Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Henan University, Kaifeng, 475004, China.
Chi Tian *Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Henan University, Kaifeng, 475004, China.
Waner Wang *Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Henan University, Kaifeng, 475004, China.
Yangyang ZhouDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Henan University, Kaifeng, 475004, China.
Xiaoqing WangDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Henan University, Kaifeng, 475004, China. wangxiaoqing@henu.edu.cn.ORCID http://orcid.org/0009-0003-5437-0779
Lei ZhangShanghai Yangzhi Rehabilitation Hospital (Shanghai Sunshine Rehabilitation Center), Tongji University School of Medicine, Shanghai, 200092, China. leizhang1120@outlook.com.

Funding

Innovation Project for College Students of Henan University No. XJ2024054 and No. XJ2024055National Natural Science Foundation of China No.82401779 and No.31371386National Resource Center for the First-Year Experience and Students in Transition, University of South Carolina No. 20243305198Natural Science Foundation of Henan Province No.232300421301Science and Technology Development in Kaifeng City No.2203009 and No.2403005
6 · The paper itself

Abstract

SATB2 is an AT-rich DNA-binding protein with a highly restricted expression pattern, primarily found in the brain, digestive tract, bone, and immune system, making it a promising target for medical research and clinical applications. Dysregulation or mutations in SATB2 have been implicated in various conditions, including cancers, isolated cleft palate, and SATB2-associated syndrome (SAS). This review aims to provide a comprehensive summary of the structure, biological functions, and potential role of SATB2 in tumor development. SATB2 influences gene regulation through epigenetic modulation, impacting various biological activities, including cell differentiation and immune responses. Recent studies have increasingly recognized its roles in tumorigenesis, including its contributions to cancer progression and metastasis. Moreover, SATB2 shows promise as a diagnostic marker and therapeutic target in oncology and bone-related disorders. Understanding its precise mechanisms in these contexts can pave the way for future advancements in therapeutic strategies. This review highlights the current state of knowledge on the roles of SATB2 and discusses its structural characteristics, biological functions, and potential implications in tumor development.

Indexed as

Epigenetic modulationGene regulationSATB2Tumor development

Identifiers

PMID40722111
PMCPMC12302682

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.