Evidence map›Paper›PMID 38861602›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Iridium(III) carbene complexes as potent girdin inhibitors against metastatic cancers.

Mei-Ling Ruan, Wen-Xiu Ni, Jacky C H Chu, Tsz-Lung Lam, Kwok-Chung Law, Yiwei Zhang, Guanya Yang, Ying He, Chunlei Zhang, Yi Man Eva Fung and 5 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 2 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

4 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. 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

15 authors.

Mei-Ling RuanLaboratory for Synthetic Chemistry and Chemical Biology Limited, Hong Kong Science Park, Shatin, Hong Kong, China.
Wen-Xiu NiDepartment of Medicinal Chemistry, Shantou University Medical College, Shantou 515041, Guangdong, China.
Jacky C H ChuLaboratory for Synthetic Chemistry and Chemical Biology Limited, Hong Kong Science Park, Shatin, Hong Kong, China.ORCID 0000-0003-3858-3312
Tsz-Lung LamState Key Laboratory of Synthetic Chemistry and Department of Chemistry, The University of Hong Kong, Pokfulam, Hong Kong, China.
Kwok-Chung LawLaboratory for Synthetic Chemistry and Chemical Biology Limited, Hong Kong Science Park, Shatin, Hong Kong, China.
Yiwei ZhangLaboratory for Synthetic Chemistry and Chemical Biology Limited, Hong Kong Science Park, Shatin, Hong Kong, China.
Guanya YangAI And Life Sciences Institute (Hong Kong) Limited, Hong Kong Science Park, Shatin, Hong Kong, China.
Ying HeAI And Life Sciences Institute (Hong Kong) Limited, Hong Kong Science Park, Shatin, Hong Kong, China.
Chunlei ZhangLaboratory for Synthetic Chemistry and Chemical Biology Limited, Hong Kong Science Park, Shatin, Hong Kong, China.ORCID 0000-0002-7781-0218
Yi Man Eva FungState Key Laboratory of Synthetic Chemistry and Department of Chemistry, The University of Hong Kong, Pokfulam, Hong Kong, China.
Tao LiuDepartment of Medicinal Chemistry, Shantou University Medical College, Shantou 515041, Guangdong, China.
Tao HuangDepartment of Medicinal Chemistry, Shantou University Medical College, Shantou 515041, Guangdong, China.
Chun-Nam LokLaboratory for Synthetic Chemistry and Chemical Biology Limited, Hong Kong Science Park, Shatin, Hong Kong, China.
Sharon Lai-Fung ChanDepartment of Applied Biology and Chemical Biology, The Hong Kong Polytechnic University, Hung Hom, Hong Kong, China.
Chi-Ming CheLaboratory for Synthetic Chemistry and Chemical Biology Limited, Hong Kong Science Park, Shatin, Hong Kong, China.ORCID 0000-0002-2554-7219

Funding

Guangdong Major Project of Basic and Applied Basic Research 2019B030302009Innovation and Technology Commission (ITC) Health@InnoHK
6 · The paper itself

Abstract

Many cancer-driving protein targets remain undruggable due to a lack of binding molecular scaffolds. In this regard, octahedral metal complexes with unique and versatile three-dimensional structures have rarely been explored as inhibitors of undruggable protein targets. Here, we describe antitumor iridium(III) pyridinium-N-heterocyclic carbene complex

Indexed as

Antineoplastic AgentsIridiumMethaneAnimalsCarcinoma, Non-Small-Cell LungCell Line, TumorCell ProliferationCoordination ComplexesHumansLung NeoplasmsMaleMiceMicrofilament ProteinsNeoplasm MetastasisTriple Negative Breast NeoplasmsXenograft Model Antitumor AssaysAntineoplastic AgentscarbeneCoordination ComplexesIridiumMethaneMicrofilament Proteinsanticancer compoundsGirdiniridiumN-heterocyclic carbene

Identifiers

PMID38861602
PMCPMC11194514

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.