Evidence map›Paper›PMID 41738039›Full record

ReviewJournal of the National Cancer Center2026

Emerging therapies to overcome antiandrogen resistance and beyond in lethal prostate cancer.

Furong Huang, Kexin Li, Jeffrey W Shevach, Qianben Wang

Abstract readReview
In one paragraph

Review in Journal of the National Cancer Center, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Targeting the PI3K/AKT/mTOR signaling pathway in prostate cancer: Molecular dysregulation, therapeutic advances, and future directions.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2026
    Review
  9. Article
  10. Article
  11. 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

4 authors.

Furong HuangDepartment of Pathology and Duke Cancer Institute Center for Prostate and Urologic Cancer, Duke University School of Medicine, Durham, United States.
Kexin LiDepartment of Pathology and Duke Cancer Institute Center for Prostate and Urologic Cancer, Duke University School of Medicine, Durham, United States.
Jeffrey W ShevachDepartment of Medicine and Duke Cancer Institute Center for Prostate and Urologic Cancer, Duke University School of Medicine, Durham, United States.
Qianben WangDepartment of Pathology and Duke Cancer Institute Center for Prostate and Urologic Cancer, Duke University School of Medicine, Durham, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer remains the second most common malignancy among men worldwide, with treatment paradigms evolving dramatically over the last two decades. Despite the longstanding efficacy of androgen deprivation therapy (ADT) and its combination with next-generation androgen receptor (AR) signaling inhibitors or chemotherapy in metastatic hormone-sensitive settings, most tumors ultimately develop resistance and progress to lethal castration-resistant prostate cancer (CRPC). This resistance often stems from a range of molecular alterations, including AR mutations, amplifications, splice variants, and tumor suppressor gene lesions (e.g.,

Indexed as

Androgen receptor signalingEmerging therapiesPrecision medicineProstate cancerTherapy resistance

Identifiers

PMID41738039
PMCPMC12925916

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.