Evidence map›Paper›PMID 33609296›Full record

ArticleCancer science2021

Cystathionine-gamma-lyase overexpression in T cells enhances antitumor effect independently of cysteine autonomy.

Melanie Lancien, Lucile Gueno, Sonia Salle, Emmanuel Merieau, Gaelle Beriou, Tuan H Nguyen, Ahmed Abidi, Nahzli Dilek, Pierre Solomon, Jeremie Poschmann and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-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

17 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. High-throughputFrontiers in cell and developmental biology · 2022
    Article
  16. Review
  17. 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 3 countries.

Melanie LancienInserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN, Université de Nantes, Nantes, France.
Lucile GuenoInserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN, Université de Nantes, Nantes, France.
Sonia SalleInserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN, Université de Nantes, Nantes, France.
Emmanuel MerieauInserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN, Université de Nantes, Nantes, France.
Gaelle BeriouInserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN, Université de Nantes, Nantes, France.
Tuan H NguyenInserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN, Université de Nantes, Nantes, France.
Ahmed AbidiInserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN, Université de Nantes, Nantes, France.
Nahzli DilekMolecular Modeling Group, SIB Swiss Institute for Bioinformatics, Lausanne, Switzerland.
Pierre SolomonInserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN, Université de Nantes, Nantes, France.
Jeremie PoschmannInserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN, Université de Nantes, Nantes, France.
Olivier MichielinMolecular Modeling Group, SIB Swiss Institute for Bioinformatics, Lausanne, Switzerland.
Romain Vuillefroy de SillyThe Ludwig Institute for Cancer Research, University of Lausanne, Epalinges, Switzerland.
Bernard VanhoveInserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN, Université de Nantes, Nantes, France.
Cedric LouvetInserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN, Université de Nantes, Nantes, France.ORCID https://orcid.org/0000-0002-5668-2448
Inserm · FRSIB Swiss Institute of Bioinformatics · CHLudwig Cancer Research · CHTunis University · TN

Funding

Agence Nationale de la Recherche ANR-11-LABX-0016-01Fondation pour la Recherche Médicale ECO20160736078
6 · The paper itself

Abstract

T cells could be engineered to overcome the aberrant metabolic milieu of solid tumors and tip the balance in favor of a long-lasting clinical response. Here, we explored the therapeutic potential of stably overexpressing cystathionine-gamma-lyase (CTH, CSE, or cystathionase), a pivotal enzyme of the transsulfuration pathway, in antitumor CD8

Indexed as

Adoptive TransferAnimalsCD8-Positive T-LymphocytesCell EngineeringCell Line, TumorCell ProliferationCystathionine gamma-LyaseCysteineExtracellular FluidFemaleGlycineMethionineMiceMice, Inbred C57BLModels, AnimalOvarian NeoplasmsCystathionine gamma-LyaseCysteineGlycineMethionineProlineSerineadoptive cell transferamino acidcysteinemetabolismT cell

Identifiers

PMID33609296
PMCPMC8088958
OpenAlexW3130155352

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.