Evidence map›Paper›PMID 35316216›Full record

ArticleThe Journal of clinical investigation2022

PHGDH is required for germinal center formation and is a therapeutic target in MYC-driven lymphoma.

Annalisa D'Avola, Nathalie Legrave, Mylène Tajan, Probir Chakravarty, Ryan L Shearer, Hamish W King, Katarina Kluckova, Eric C Cheung, Andrew J Clear, Arief S Gunawan and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. A guide to B cell metabolism.Nature reviews. Immunology · 2026
    Review
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  5. ODC1 restricts meningeal B cell age-associated-like phenotype and function in multiple sclerosis: A human and experimental study.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 3 institutions in 2 countries.

Annalisa D'AvolaThe Francis Crick Institute, London, United Kingdom.
Nathalie LegraveThe Francis Crick Institute, London, United Kingdom.
Mylène TajanThe Francis Crick Institute, London, United Kingdom.
Probir ChakravartyThe Francis Crick Institute, London, United Kingdom.
Ryan L ShearerCentre for Haemato-Oncology, Barts Cancer Institute, and.
Hamish W KingCentre for Immunobiology, Blizard Institute, Queen Mary University of London, London, United Kingdom.
Katarina KluckovaCentre for Haemato-Oncology, Barts Cancer Institute, and.
Eric C CheungThe Francis Crick Institute, London, United Kingdom.
Andrew J ClearCentre for Haemato-Oncology, Barts Cancer Institute, and.
Arief S GunawanThe Francis Crick Institute, London, United Kingdom.
Lingling ZhangThe Francis Crick Institute, London, United Kingdom.
Louisa K JamesCentre for Immunobiology, Blizard Institute, Queen Mary University of London, London, United Kingdom.
James I MacRaeMetabolomics Science Technology Platform, The Francis Crick Institute, London, United Kingdom.
John G GribbenCentre for Haemato-Oncology, Barts Cancer Institute, and.
Dinis P CaladoThe Francis Crick Institute, London, United Kingdom.
Karen H VousdenThe Francis Crick Institute, London, United Kingdom.
John C RichesThe Francis Crick Institute, London, United Kingdom.
The Francis Crick Institute · GBCancer Institute (WIA) · INQueen Mary University of London · GB

Funding

Cancer Research UK 16857Cancer Research UK C355/A25137Cancer Research UK C596/A26855Cancer Research UK FC001057Medical Research Council FC001057Medical Research Council MR/J008060/1Wellcome Trust 110020/Z/15/ZWellcome Trust 213555/Z/18/ZWellcome Trust FC001057Wellcome Trust FC001557
6 · The paper itself

Abstract

The synthesis of serine from glucose is a key metabolic pathway supporting cellular proliferation in healthy and malignant cells. Despite this, the role that this aspect of metabolism plays in germinal center biology and pathology is not known. Here, we performed a comprehensive characterization of the role of the serine synthesis pathway in germinal center B cells and lymphomas derived from these cells. We demonstrate that upregulation of a functional serine synthesis pathway is a metabolic hallmark of B cell activation and the germinal center reaction. Inhibition of phosphoglycerate dehydrogenase (PHGDH), the first and rate-limiting enzyme in this pathway, led to defective germinal formation and impaired high-affinity antibody production. In addition, overexpression of enzymes involved in serine synthesis was a characteristic of germinal center B cell-derived lymphomas, with high levels of expression being predictive of reduced overall survival in diffuse large B cell lymphoma. Inhibition of PHGDH induced apoptosis in lymphoma cells, reducing disease progression. These findings establish PHGDH as a critical player in humoral immunity and a clinically relevant target in lymphoma.

Indexed as

LymphomaLymphoma, B-CellCell ProliferationGerminal CenterHumansPhosphoglycerate DehydrogenaseSerinePhosphoglycerate DehydrogenaseSerineAmino acid metabolismImmunoglobulinsImmunologyLymphomasMetabolism

Identifiers

PMID35316216
PMCPMC9057607
OpenAlexW4220665797

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.