Evidence map›Paper›PMID 31936496›Full record

ReviewMolecules (Basel, Switzerland)2020

Rationally Designed Ruthenium Complexes for Breast Cancer Therapy.

Golara Golbaghi, Annie Castonguay

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Article
  2. Article
  3. Ru-Based NSAIDs as Potential Anticancer Therapeutics.Molecules (Basel, Switzerland) · 2026
    Article
  4. Article
  5. Review
  6. Therapeutic Potential of Metal-Based and PARP Inhibitor Chemotherapy forInternational journal of molecular sciences · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors.

Golara GolbaghiOrganometallic Chemistry Laboratory for the Design of Catalysts and Therapeutics, INRS-Centre Armand-Frappier Santé Biotechnologie, Université du Québec, Laval, QC H7V 1B7, Canada.
Annie CastonguayOrganometallic Chemistry Laboratory for the Design of Catalysts and Therapeutics, INRS-Centre Armand-Frappier Santé Biotechnologie, Université du Québec, Laval, QC H7V 1B7, Canada.ORCID 0000-0001-5705-6353

Funding

Canada Foundation for Innovation 34846Fonds de Recherche du Québec Santé 32622Natural Sciences and Engineering Research Council of Canada 06336
6 · The paper itself

Abstract

Since the discovery of the anticancer potential of ruthenium-based complexes, several species were reported as promising candidates for the treatment of breast cancer, which accounts for the greatest number of new cases in women every year worldwide. Among these ruthenium complexes, species containing bioactive ligand(s) have attracted increasing attention due to their potential multitargeting properties, leading to anticancer drug candidates with a broader range of cellular targets/modes of action. This review of the literature aims at providing an overview of the rationally designed ruthenium-based complexes that have been reported to date for which ligands were carefully selected for the treatment of hormone receptor positive breast cancers (estrogen receptor (ER+) or progesterone receptor (PR+)). In addition, this brief survey highlights some of the most successful examples of ruthenium complexes reported for the treatment of triple negative breast cancer (TNBC), a highly aggressive type of cancer, regardless of if their ligands are known to have the ability to achieve a specific biological function.

Indexed as

Antineoplastic AgentsCoordination ComplexesErb-b2 Receptor Tyrosine KinasesFemaleHumansLigandsReceptors, EstrogenReceptors, ProgesteroneRutheniumTriple Negative Breast NeoplasmsAntineoplastic AgentsCoordination ComplexesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesLigandsReceptors, EstrogenReceptors, ProgesteroneRutheniumbreast cancerenzyme inhibitionhormone positive breast cancermetallodrugmultitargeted therapyrutheniumtriple negative breast cancer (TNBC)

Identifiers

PMID31936496
PMCPMC7024301

What OpenQuestion holds

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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.