Evidence map›Paper›PMID 35458687›Full record

ReviewMolecules (Basel, Switzerland)2022

Recent Advances in Synergistic Antitumor Effects Exploited from the Inhibition of Ataxia Telangiectasia and RAD3-Related Protein Kinase (ATR).

Li-Wei Wang, Songwei Jiang, Ying-Hui Yuan, Jilong Duan, Nian-Dong Mao, Zi Hui, Renren Bai, Tian Xie, Xiang-Yang Ye

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Design, synthesis and anti-breast cancer activity evaluation of 6,7-dihydro-5Journal of enzyme inhibition and medicinal chemistry · 2026
    Article
  3. Pg-Induced ATR Activation Promotes ESCC Progression via M2 TAM Polarization.Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Advances in molecular targeted therapies to increase efficacy of (chemo)radiation therapy.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2023
    Review
  10. 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

9 authors at 1 institution in 1 country.

Li-Wei WangSchool of Pharmacy, Hangzhou Normal University, Hangzhou 311121, China.
Songwei JiangSchool of Pharmacy, Hangzhou Normal University, Hangzhou 311121, China.
Ying-Hui YuanSchool of Pharmacy, Hangzhou Normal University, Hangzhou 311121, China.
Jilong DuanSchool of Pharmacy, Hangzhou Normal University, Hangzhou 311121, China.
Nian-Dong MaoSchool of Pharmacy, Hangzhou Normal University, Hangzhou 311121, China.
Zi HuiSchool of Pharmacy, Hangzhou Normal University, Hangzhou 311121, China.
Renren BaiSchool of Pharmacy, Hangzhou Normal University, Hangzhou 311121, China.ORCID 0000-0002-3511-5794
Tian XieSchool of Pharmacy, Hangzhou Normal University, Hangzhou 311121, China.ORCID 0000-0001-7066-1443
Xiang-Yang YeSchool of Pharmacy, Hangzhou Normal University, Hangzhou 311121, China.ORCID 0000-0003-3739-0930
Hangzhou Normal University · CN

Funding

Hangzhou City "115" plan to introduce overseas intelligence projects 20200215 and 20210120National Natural Science Foundation of China 82073686, 81730108, and 81973635Scientific Research Foundation for Scholars of Hangzhou Normal University 2019QDL003the Ministry of Science and Technology of China (High-end foreign experts program G20200217005 and G2021017004
6 · The paper itself

Abstract

As one of the key phosphatidylinositol 3-kinase-related kinases (PIKKs) family members, ataxia telangiectasia and RAD3-related protein kinase (ATR) is crucial in maintaining mammalian cell genomic integrity in DNA damage response (DDR) and repair pathways. Dysregulation of ATR has been found across different cancer types. In recent years, the inhibition of ATR has been proven to be effective in cancer therapy in preclinical and clinical studies. Importantly, tumor-specific alterations such as ATM loss and Cyclin E1 (CCNE1) amplification are more sensitive to ATR inhibition and are being exploited in synthetic lethality (SL) strategy. Besides SL, synergistic anticancer effects involving ATRi have been reported in an increasing number in recent years. This review focuses on the recent advances in different forms of synergistic antitumor effects, summarizes the pharmacological benefits and ongoing clinical trials behind the biological mechanism, and provides perspectives for future challenges and opportunities. The hope is to draw awareness to the community that targeting ATR should have great potential in developing effective anticancer medicines.

Indexed as

Ataxia TelangiectasiaNeoplasmsAnimalsAtaxia Telangiectasia Mutated ProteinsDNA DamageMammalsProtein KinasesAtaxia Telangiectasia Mutated ProteinsProtein Kinasesataxia telangiectasia and RAD3-related protein kinase (ATR)cancer therapyDNA damage response (DDR)inhibitorsynergistic effects

Identifiers

PMID35458687
PMCPMC9029554
OpenAlexW4224308750

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.