Evidence map›Paper›PMID 34613635›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2022

Cycloruthenated Self-Assembly with Metabolic Inhibition to Efficiently Overcome Multidrug Resistance in Cancers.

Jia Li, Leli Zeng, Zheng Wang, Hengxing Chen, Shuo Fang, Jinquan Wang, Chao-Yun Cai, Enming Xing, Xinxing Liao, Zhi-Wei Li and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 50 citations in OpenAlex.

  1. Cycloruthenated Imines: A Step into the Nanomolar Region.Molecules (Basel, Switzerland) · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. A Novel Substituted Benzo[Journal of medicinal chemistry · 2024
    Article
  6. Article
  7. Review
  8. Article
  9. A cycloruthenated complex, ruthenium (II) Z (RuZ) overcomesJournal of translational internal medicine · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
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

14 authors at 4 institutions in 2 countries.

Jia LiGuangdong Provincial Key Laboratory of Digestive Cancer Research, Precision Medicine Center, The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, Guangdong, 518107, P. R. China.
Leli ZengGuangdong Provincial Key Laboratory of Digestive Cancer Research, Precision Medicine Center, The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, Guangdong, 518107, P. R. China.
Zheng WangCollege of Chemistry and Chemical Engineering, Key Laboratory of Chemical Additives for China National Light Industry, Shaanxi University of Science and Technology, Xi'an, 710021, P. R. China.
Hengxing ChenGuangdong Provincial Key Laboratory of Digestive Cancer Research, Precision Medicine Center, The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, Guangdong, 518107, P. R. China.
Shuo FangGuangdong Provincial Key Laboratory of Digestive Cancer Research, Precision Medicine Center, The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, Guangdong, 518107, P. R. China.
Jinquan WangGuangdong Province Key Laboratory for Biotechnology Drug Candidates, School of Bioscience and Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, 510006, P. R. China.
Chao-Yun CaiCollege of Pharmacy and Health Sciences, St. John's University, New York, NY, 11439, USA.
Enming XingGuangdong Provincial Key Laboratory of Digestive Cancer Research, Precision Medicine Center, The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, Guangdong, 518107, P. R. China.
Xinxing LiaoMOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-Sen University, Guangzhou, 510275, P. R. China.
Zhi-Wei LiMOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-Sen University, Guangzhou, 510275, P. R. China.
Charles R AshbyCollege of Pharmacy and Health Sciences, St. John's University, New York, NY, 11439, USA.
Zhe-Sheng ChenCollege of Pharmacy and Health Sciences, St. John's University, New York, NY, 11439, USA.ORCID https://orcid.org/0000-0002-8289-097X
Hui ChaoGuangdong Provincial Key Laboratory of Digestive Cancer Research, Precision Medicine Center, The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, Guangdong, 518107, P. R. China.
Yihang PanGuangdong Provincial Key Laboratory of Digestive Cancer Research, Precision Medicine Center, The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, Guangdong, 518107, P. R. China.
Sun Yat-sen University · CNSt. John's University · USGuangdong Pharmaceutical University · CNShaanxi University of Science and Technology · CN

Funding

Guangdong Basic and Applied Basic Research Foundation 2021A1515010117Guangdong Provincial Key Laboratory of Digestive Cancer Research 2021B1212040006National Key Research and Development Program of China 2018YFA0902801National Natural Science Foundation of China 21771042National Natural Science Foundation of China 21807073Research Start-up Fund of the Seventh Affiliated Hospital, Sun Yat-sen University 593009Talents Program of Sun Yat-sen University ZSQYBRJH0001
6 · The paper itself

Abstract

The synthesis and the evaluation of the efficacy of a cycloruthenated complex, RuZ, is reported, to overcome multi-drug resistance (MDR) in cancer cells. RuZ can self-assemble into nanoaggregates in the cell culture medium, resulting in a high intracellular concentration of RuZ in MDR cancer cells. The self-assembly significantly decreases oxygen consumption and inhibits glycolysis, which decreases cellular adenosine triphosphate (ATP) levels. The decrease in ATP levels and its low affinity for the ABCB1 and ABCG2 transporters (which mediate MDR) significantly increase the retention of RuZ by MDR cancer cells. Furthermore, RuZ increases cellular oxidative stress, inducing DNA damage, and, in combination with the aforementioned effects of RuZ, increases the apoptosis of cancer cells. Proteomic profiling analysis suggests that the RuZ primarily decreases the expression of proteins that mediate glycolysis and aerobic mitochondrial respiration and increases the expression of proteins involved in apoptosis. RuZ inhibits the proliferation of 35 cancer cell lines, of which 7 cell lines are resistant to clinical drugs. It is also active in doxorubicin-resistant MDA-MB-231/Adr mouse tumor xenografts. To the best of our knowledge, the results are the first to show that self-assembled cycloruthenated complexes are efficacious in inhibiting the growth of MDR cancer cells.

Indexed as

Antineoplastic AgentsNeoplasmsAnimalsATP Binding Cassette Transporter, Subfamily G, Member 2Cell Line, TumorDoxorubicinDrug Resistance, MultipleDrug Resistance, NeoplasmHumansMiceProteomicsAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily G, Member 2Doxorubicinantitumor agentscyclometalated ruthenium complexesmetabolism inhibitionmultidrug resistanceself-assembly

Identifiers

PMID34613635
PMCPMC11468970
OpenAlexW3204337430

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.