Evidence map›Paper›PMID 27765921›Full record

ReviewOncotarget2017

Triple-negative breast cancer: is there a treatment on the horizon?

Hui Yao, Guangchun He, Shichao Yan, Chao Chen, Liujiang Song, Thomas J Rosol, Xiyun Deng

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 208 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
208citing papers in PubMed, 4 pooled it
11.3field-weighted citation impact, top 1% of its field
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

208 citing papers in PubMed, 4 syntheses or guidelines pooled it, 403 citations in OpenAlex.

  1. Pooled it
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  5. Trial
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  7. Article
  8. Review
  9. Actinolactomycin fromMolecules (Basel, Switzerland) · 2026
    Article
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  13. Survivin targeting triple-fusion vaccineMedical oncology (Northwood, London, England) · 2025
    Article
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  16. Review
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  18. Article
  19. Review
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148 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 2 countries.

Hui YaoDepartment of Pathology, Hunan Normal University Medical College, Changsha, Hunan, China.
Guangchun HeDepartment of Pathology, Hunan Normal University Medical College, Changsha, Hunan, China.
Shichao YanDepartment of Pathology, Hunan Normal University Medical College, Changsha, Hunan, China.
Chao ChenDepartment of Pathology, Hunan Normal University Medical College, Changsha, Hunan, China.
Liujiang SongDepartment of Pediatrics, Hunan Normal University Medical College, Changsha, Hunan, China.
Thomas J RosolDepartment of Veterinary Biosciences, The Ohio State University, Columbus, Ohio, USA.
Xiyun DengDepartment of Pathology, Hunan Normal University Medical College, Changsha, Hunan, China.
Hunan Normal University · CNThe Ohio State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC), which accounts for 15-20% of all breast cancers, does not express estrogen receptor (ER) or progesterone receptor (PR) and lacks human epidermal growth factor receptor 2 (HER2) overexpression or amplification. These tumors have a more aggressive phenotype and a poorer prognosis due to the high propensity for metastatic progression and absence of specific targeted treatments. Patients with TNBC do not benefit from hormonal or trastuzumab-based targeted therapies because of the loss of target receptors. Although these patients respond to chemotherapeutic agents such as taxanes and anthracyclines better than other subtypes of breast cancer, prognosis remains poor. A group of targeted therapies under investigation showed favorable results in TNBC, especially in cancers with BRCA mutation. The lipid-lowering statins (3-hydroxy-3-methyl-glutaryl coenzyme A reductase inhibitors), including lovastatin and simvastatin, have been shown to preferentially target TNBC compared with non-TNBC. These statins hold great promise for the management of TNBC. Only with the understanding of the molecular basis for the preference of statins for TNBC and more investigations in clinical trials can they be reformulated into a clinically approved drug against TNBC.

Indexed as

AnthracyclinesAntineoplastic AgentsBRCA1 ProteinBRCA2 ProteinErb-b2 Receptor Tyrosine KinasesFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsLovastatinMolecular Targeted TherapyReceptors, EstrogenReceptors, ProgesteroneSimvastatinTaxoidsTriple Negative Breast NeoplasmsAnthracyclinesAntineoplastic AgentsBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesHydroxymethylglutaryl-CoA Reductase InhibitorsLovastatinReceptors, EstrogenReceptors, ProgesteroneSimvastatinTaxoidsbreast cancertherapeuticstriple-negative

Identifiers

PMID27765921
PMCPMC5352107
OpenAlexW2523763608

What OpenQuestion 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 OpenQuestion graph.