Evidence map›Paper›PMID 40003864›Full record

ReviewInternational journal of molecular sciences2025

Divide and Conquer-Targeted Therapy for Triple-Negative Breast Cancer.

Milica Nedeljković, Ana Vuletić, Katarina Mirjačić Martinović

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

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

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

  1. Pooled it
  2. Review
  3. Article
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  6. Article
  7. Review
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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

3 authors.

Milica NedeljkovićDepartment of Experimental Oncology, Institute for Oncology and Radiology of Serbia, 11000 Belgrade, Serbia.ORCID 0000-0003-0153-3901
Ana VuletićDepartment of Experimental Oncology, Institute for Oncology and Radiology of Serbia, 11000 Belgrade, Serbia.
Katarina Mirjačić MartinovićDepartment of Experimental Oncology, Institute for Oncology and Radiology of Serbia, 11000 Belgrade, Serbia.

Funding

Ministry of Science, Technological Development and Innovation of the Republic of Serbia 451-03-66/2024-03/200043
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is the most aggressive and malignant type of breast cancer with limited treatment options and poor prognosis. One of the most significant impediments in TNBC treatment is the high heterogeneity of this disease, as highlighted by the detection of several molecular subtypes of TNBC. Each subtype is driven by distinct mutations and pathway aberrations, giving rise to specific molecular characteristics closely connected to clinical behavior, outcomes, and drug sensitivity. This review summarizes the knowledge regarding TNBC molecular subtypes and how it can be harnessed to devise tailored treatment strategies instead of blindly using targeted drugs. We provide an overview of novel targeted agents and key insights about new treatment modalities with an emphasis on the androgen receptor signaling pathway, cancer stem cell-associated pathways, phosphatidylinositol 3-kinase (PI3K)/AKT pathway, growth factor signaling, and immunotherapy.

Indexed as

Antineoplastic AgentsMolecular Targeted TherapyTriple Negative Breast NeoplasmsFemaleHumansImmunotherapyNeoplastic Stem CellsProto-Oncogene Proteins c-aktReceptors, AndrogenSignal TransductionAntineoplastic AgentsProto-Oncogene Proteins c-aktReceptors, Androgenandrogen receptorEGFRimmune checkpoint inhibitorsimmunotherapyJAK/STAT pathwaymolecular subtypesnotch pathwayPARP inhibitorsPI3K/AKT pathwayTGF-β pathwaytriple-negative breast cancerVEGFRWnt/β-catenin pathway

Identifiers

PMID40003864
PMCPMC11855393

What OpenQuestion holds

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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.