Evidence mapPaperPMID 41608619Full record

ReviewInternational journal of biological sciences2026

The Role of Estrogen Signaling Pathway and Targeted Therapy Exploration in Urological Tumors.

Cunzhen Ma, Lin Yang, Weijia Li, Wentai Shangguan, Wenxue Huang, Zhuohang Li, Boyuan Sun, Xunguo Yang, Haoxiang Xu, Zhibiao Li and 4 more

Abstract readReview
In one paragraph

Review in International journal of biological sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

14 authors.

Cunzhen MaDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Lin YangDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Weijia LiDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Wentai ShangguanDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Wenxue HuangDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Zhuohang LiDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Boyuan SunDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Xunguo YangDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Haoxiang XuDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Zhibiao LiDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Peidan PengDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Zongwei WangDepartment of Surgery, Division of Urology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Peng WuDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Bisheng ChengDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Estrogen signaling has emerged as a pivotal regulator in the development and progression of various cancers, including those of the urological system. While urological malignancies have traditionally been linked with androgen signaling, recent studies reveal a complex interplay where estrogen receptors-ERα, ERβ, and GPER-modulate critical cellular processes such as proliferation, apoptosis, and metastasis in these cancers. Here we show that estrogen receptors, through both genomic and non-genomic pathways, exert dual roles in either promoting or inhibiting tumor growth, making them both a challenge and a potential therapeutic target. These insights suggest that targeting estrogen receptor pathways could offer novel treatment strategies, especially for advanced or therapy-resistant urological tumors.Furthermore, understanding the molecular mechanisms through which estrogen receptors influence tumor progression could lead to the development of more specific and less toxic treatment options. The findings not only shift the paradigm of estrogen's role in cancer biology but also underscore the potential for personalized treatments, where estrogen receptor status could be used to tailor more effective and individualized therapeutic regimens. This review ushers in new possibilities for advancing urological oncology, where estrogen signaling may hold the key to overcoming current therapeutic challenges and improving clinical outcomes.

Indexed as

EstrogensUrologic NeoplasmsAnimalsEstrogen Receptor alphaHumansReceptors, EstrogenSignal TransductionEstrogen Receptor alphaEstrogensReceptors, EstrogenERα and ERβestrogen receptorsestrogen signalingGPERtargeted therapyurological tumors

Identifiers

PMID41608619
PMCPMC12836535

What Socratic holds

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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.