Evidence map›Paper›PMID 40776679›Full record

ReviewFuture medicinal chemistry2025

Small molecule inhibitors for treating breast cancer: drug analysis based on the pathogenesis of breast cancer.

Yu Jiang, Zihua Tang, Wenyue Zheng, Xue Xiao

Abstract readReview
In one paragraph

Review in Future medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yu JiangWest China Hospital of Stomatology, Sichuan University, Chengdu, China.
Zihua TangWest China Hospital of Stomatology, Sichuan University, Chengdu, China.
Wenyue ZhengDepartment of Pediatric Dentistry, West China Second University Hospital, Sichuan University, Chengdu, China.
Xue XiaoMinistry of Education, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer (BC) is characterized by the abnormal and rapid growth of breast epithelial cells, driven by various carcinogenic factors. Advances in understanding the signaling pathways and molecular mechanisms involved in BC progression have facilitated the development of small molecule inhibitors for its treatment. Significant progress has been made in creating inhibitors that target the PI3K/AKT/mTOR signaling pathway. Current clinical research focuses on compounds such as GDC-0077 and NVP-BKM120, advancing into phase II/III clinical trials. Preclinical drugs like NVP-CLR457, AZD6482, PF-06843195, and GDC-0326 show promising potential for further optimization and entry into BC clinical trials. This review aims to provide an overview of the clinical and preclinical development of small molecule inhibitors for various molecular subtypes of BC, emphasizing their structural composition, therapeutic outcomes, and mechanisms of action. Additionally, we highlight key targets and pathways involved in BC pathogenesis, offering essential insights for the design of effective therapeutic agents for breast cancer.

Indexed as

Antineoplastic AgentsBreast NeoplasmsProtein Kinase InhibitorsSmall Molecule LibrariesAnimalsFemaleHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionTOR Serine-Threonine KinasesAntineoplastic AgentsPhosphatidylinositol 3-KinasesProtein Kinase InhibitorsProto-Oncogene Proteins c-aktSmall Molecule LibrariesTOR Serine-Threonine KinasesBreast cancerpathogenesissmall molecule inhibitorstructure-activity relationships (SARs)targeted therapy

Identifiers

PMID40776679
PMCPMC12506733

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.