Evidence map›Paper›PMID 39249180›Full record

ReviewCell biochemistry and biophysics2025

Targeting HSP90 in Gynecologic Cancer: Molecular Mechanisms and Therapeutic Approaches.

Lu Min, Xuewei Li, Lily Liang, Zheng Ruan, Shaohui Yu

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cell biochemistry and biophysics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Lu MinChangchun University of Chinese Medicine Hospital, Changchun, 130000, China.
Xuewei LiChangchun University of Chinese Medicine Hospital, Changchun, 130000, China.
Lily LiangChangchun University of Chinese Medicine Hospital, Changchun, 130000, China.
Zheng RuanDepartment of Traditional Chinese Medicine, 964th Hospital, Changchun, 130000, China.
Shaohui YuChangchun University of Chinese Medicine Hospital, Changchun, 130000, China. 18686513999@126.com.ORCID http://orcid.org/0009-0007-2350-6249

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the leading causes of mortality for women is gynecologic cancer (GC). Numerous molecules (tumor suppressor genes or oncogenes) are involved in this form of cancer's invasion, metastasis, tumorigenic process, and therapy resistance. Currently, there is a shortage of efficient methods to eliminate these diseases, hence it is crucial to carry out more extensive studies on GCs. Novel pharmaceuticals are required to surmount this predicament. Highly conserved molecular chaperon, heat shock protein (HSP) 90, is essential for the maturation of recently produced polypeptides and offers a refuge for misfolding or denatured proteins to be turned around. In cancer, the client proteins of HSP90 play a role in the entire process of oncogenesis, which is linked to all the characteristic features of cancer. In this study, we explore the various functions of HSPs in GC progression. We also discuss their potential as promising targets for pharmacological therapy.

Indexed as

Antineoplastic AgentsGenital Neoplasms, FemaleHSP90 Heat-Shock ProteinsMolecular Targeted TherapyAnimalsFemaleHumansAntineoplastic AgentsHSP90 Heat-Shock ProteinsCervical cancerEndometrial cancerGynecologic cancerHSP90Ovarian cancer

Identifiers

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Registered trials

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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.