Evidence map›Paper›PMID 39595579›Full record

ReviewBiomolecules2024

Research Advances in Adenomyosis-Related Signaling Pathways and Promising Targets.

Hongyu Zhang, Chaoming Li, Wenyan Li, Wenhu Xin, Tiansheng Qin

Abstract readReview
In one paragraph

Review in Biomolecules, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–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

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  12. Divergent Associations of the VEGF (Medicina (Kaunas, Lithuania) · 2026
    Article
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  20. ExploringJournal of inflammation research · 2025
    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

5 authors.

Hongyu ZhangDepartment of Gynecology, The Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou 730000, China.
Chaoming LiDepartmemt of Urology, The First People's Hospital of Longnan, Longnan 742500, China.
Wenyan LiDepartment of Gynecology, The Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou 730000, China.
Wenhu XinDepartment of Gynecology, The Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou 730000, China.
Tiansheng QinDepartment of Gynecology, The Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou 730000, China.

Funding

Corporation Science Foundation of Gansu Province 24JRRA931Cuiying Scientific and Technological Innovation Program of Lanzhou University Second Hospital CY2023-MS-B13Natural Science Foundation of Gansu Province 23JRRA1301Natural Science Foundation of Gansu Province 24JRRA329Talent introduction Project of the Second Hospital of Lanzhou University yjrckyqdj-2024-02
6 · The paper itself

Abstract

Adenomyosis is a benign gynecological condition characterized by the proliferation of the endometrial stroma and glands into the myometrium, uterine volume enlargement, and peripheral smooth muscle hypertrophy. The typical clinical symptoms include chronic pelvic pain, abnormal uterine bleeding, and subfertility, all of which significantly impact quality of life. There are no effective prevention or treatment strategies for adenomyosis, partly due to a limited understanding of the pathological mechanisms underlying the initiation and progression of the disease. Given that signaling pathways play a crucial role in the development of adenomyosis, a better understanding of these signaling pathways is essential for identifying therapeutic targets and advancing drug development. The occurrence and progression of adenomyosis are closely linked to various underlying pathophysiological mechanisms, including proliferation, migration, invasion, fibrosis, angiogenesis, inflammation, oxidative stress, immune response, and epigenetic changes. This review summarizes the signaling pathways and targets associated with the pathogenesis of adenomyosis, including CXCL/CXCR, NLRP3, NF-κB, TGF-β/smad, VEGF, Hippo/YAP, PI3K/Akt/mTOR, JAK/STAT, and other relevant pathways. In addition, it identifies promising future targets for the development of adenomyosis treatment, such as m6A, GSK3β, sphks, etc.

Indexed as

AdenomyosisSignal TransductionAnimalsFemaleHumansadenomyosismolecular medicinepathophysiologypathwaystargets

Identifiers

PMID39595579
PMCPMC11591984

What Socratic holds

Textmetadata
LicenceCC BY
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.