Evidence map›Paper›PMID 29497138›Full record

ArticleCell research2018

Anti-mitotic chemotherapeutics promote apoptosis through TL1A-activated death receptor 3 in cancer cells.

Chen Qi, Xin Wang, Zhirong Shen, She Chen, Hong Yu, Noelle Williams, Gelin Wang

Open access · hybridAbstract read
In one paragraph

Article in Cell research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. TL1A induces apoptosis via DR3 in grass carp (Fish and shellfish immunology reports · 2023
    Article
  8. Article
  9. Chemotherapy: how to reduce its adverse effects while maintaining the potency?Medical oncology (Northwood, London, England) · 2023
    Review
  10. Article
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  13. Review
  14. Article
  15. Article
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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

7 authors at 4 institutions in 2 countries.

Chen QiSchool of Pharmaceutical Sciences, Tsinghua University, Beijing, 100084, China.
Xin WangSchool of Pharmaceutical Sciences, Tsinghua University, Beijing, 100084, China.
Zhirong ShenBeiGene, Beijing, 102206, China.
She ChenNational Institute of Biological Sciences, Beijing, 102206, China.
Hong YuDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX, 75390-9152, USA.
Noelle WilliamsDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX, 75390-9152, USA.
Gelin WangSchool of Pharmaceutical Sciences, Tsinghua University, Beijing, 100084, China. gelinwang@tsinghua.edu.cn.
Tsinghua University · CNThe University of Texas Southwestern Medical Center · USBeiGene (China) · CNNational Institute of Biological Sciences, Beijing · CN

Funding

Structure guided discovery of small molecule antagonists of Smac (DIABLO)/XIPAP01CA095471 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MCKNIGHT, STEVEN L · 2002 to 2011
$34.1M
NCI NIH HHS P01 CA095471
6 · The paper itself

Abstract

The commonly used antimitotic chemotherapeutic agents such as taxol and vinblastine arrest cell cycle progression by disrupting mitotic spindles, and cause cancer cells to undergo apoptosis through 'mitotic catastrophe'. The molecular mechanisms by which these drugs induce apoptosis and their relevance to clinical efficacy are not known. Facilitated by a new spindle poison diazonamide, we found that apoptosis induced by these agents requires death receptor 3 (DR3). Mitotic arrest by these agents induces lysosome-dependent secretion of the DR3 ligand, TL1A. Engagement of TL1A with DR3 stimulates the formation of FADD-containing and caspase-8-containing death-inducing signaling complex (DISC), which subsequently activates apoptosis in cells that express DR3. Expression of DR3 and TL1A correlates with the apoptotic response of human tumor xenograft models and human cancer cell lines to antimitotic drugs, providing further evidence that these drugs kill cancer cells through the DR3/TL1A-mediated pathway. These results suggest that TL1A and DR3 may hold promise to be used as biomarkers for predicting clinical response to antimitotic therapeutics.

Indexed as

AnimalsAntimitotic AgentsAntineoplastic AgentsApoptosisAutocrine CommunicationCaspase 8Cell Cycle CheckpointsCell Line, TumorLigandsMice, NudeM Phase Cell Cycle CheckpointsNeoplasmsOxazolesPaclitaxelReceptors, Tumor Necrosis Factor, Member 25Recombinant ProteinsAntimitotic AgentsAntineoplastic AgentsCaspase 8LigandsOxazolesPaclitaxelReceptors, Tumor Necrosis Factor, Member 25Recombinant ProteinsTNFRSF25 protein, humanTNFSF15 protein, humanTumor Necrosis Factor Ligand Superfamily Member 15

Identifiers

PMID29497138
PMCPMC5951888
OpenAlexW2791764667

What OpenQuestion holds

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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.