Evidence map›Paper›PMID 30007403›Full record

ReviewMolecular cancer2018

Therapeutic landscape in mutational triple negative breast cancer.

Yaqin Shi, Juan Jin, Wenfei Ji, Xiaoxiang Guan

Open access · goldAbstract readReview
In one paragraph

Review in Molecular cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
4.2field-weighted citation impact, top 4% 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

73 citing papers in PubMed, 110 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Genomic Alterations in Quadruple-Negative Breast Cancer Tumors.International journal of molecular sciences · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
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  16. Review
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  18. Review
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  20. Article

13 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

4 authors at 2 institutions in 1 country.

Yaqin ShiDepartment of Medical Oncology, Jinling Hospital, Medical School of Nanjing University, Nanjing, 210002, China.
Juan JinDepartment of Medical Oncology, Jinling Hospital, Medical School of Nanjing University, Nanjing, 210002, China.
Wenfei JiDepartment of Medical Oncology, Jinling Clinical College, Nanjing Medical University, Nanjing, 210002, China.
Xiaoxiang GuanDepartment of Medical Oncology, Jinling Hospital, Medical School of Nanjing University, Nanjing, 210002, China. xguan@nju.edu.cn.ORCID 0000-0003-3382-7808
Nanjing General Hospital of Nanjing Military Command · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple negative breast cancer (TNBC) is a heterogeneous disease with aggressive behavior and poor prognosis. Genomic sequencing has detected a distinctive mutational portrait of both the germline and somatic alterations in TNBC, which is staggeringly different from other breast cancer subtypes. The clinical utility of sequencing germline BRCA1/2 genes has been well established in TNBC. However, for other predisposition genes, studies concerning the risk and penetrance to TNBC are relatively scarce. Very few recurrent mutations, including TP53 and PI3KCA mutations, together with a long tail of individually rare mutations occur in TNBC. These combined effects of genomic alterations drive TNBC progression. Given the complexity and heterogeneity of TNBC, clinical interpretation of the genomic alterations in TNBC may pave a new way for the treatment of TNBC. In this review, we summarized the germline and somatic mutation profiles of TNBC and discussed the current and upcoming therapeutic strategies targeting the mutant proteins or pathways to enable tailored-therapeutics.

Indexed as

AdultAntineoplastic AgentsBRCA1 ProteinBRCA2 ProteinClinical Trials as TopicDNA Mutational AnalysisFemaleGerm-Line MutationHumansMiddle AgedMolecular Targeted TherapyNuclear ProteinsTranscription FactorsTriple Negative Breast NeoplasmsTumor Suppressor Protein p53Antineoplastic AgentsBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanNuclear ProteinsPI3KCA protein, humanTP53 protein, humanTranscription FactorsTumor Suppressor Protein p53GermlineMutationSomaticTherapeuticTNBC

Identifiers

PMID30007403
PMCPMC6046102
OpenAlexW2883471350

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.