Evidence map›Paper›PMID 27819051›Full record

ArticleScience advances2016

Serine one-carbon catabolism with formate overflow.

Johannes Meiser, Sergey Tumanov, Oliver Maddocks, Christiaan Fred Labuschagne, Dimitris Athineos, Niels Van Den Broek, Gillian M Mackay, Eyal Gottlieb, Karen Blyth, Karen Vousden and 2 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

114 citing papers in PubMed, 186 citations in OpenAlex.

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  20. Tracing the Diverse Paths of One-Carbon Metabolism in Cancer and Beyond.Cold Spring Harbor perspectives in medicine · 2024
    Review

54 more citing papers are in PubMed but not listed here.

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

12 authors at 2 institutions in 1 country.

Johannes MeiserCancer Research UK Beatson Institute, Glasgow, UK.ORCID 0000-0002-9093-6210
Sergey TumanovCancer Research UK Beatson Institute, Glasgow, UK; Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID 0000-0002-0557-3153
Oliver MaddocksInstitute of Cancer Sciences, University of Glasgow, Glasgow, UK.
Christiaan Fred LabuschagneCancer Research UK Beatson Institute, Glasgow, UK.
Dimitris AthineosCancer Research UK Beatson Institute, Glasgow, UK.ORCID 0000-0001-5298-7941
Niels Van Den BroekCancer Research UK Beatson Institute, Glasgow, UK.
Gillian M MackayCancer Research UK Beatson Institute, Glasgow, UK.
Eyal GottliebCancer Research UK Beatson Institute, Glasgow, UK.ORCID 0000-0002-9770-0956
Karen BlythCancer Research UK Beatson Institute, Glasgow, UK.
Karen VousdenCancer Research UK Beatson Institute, Glasgow, UK.
Jurre J KamphorstCancer Research UK Beatson Institute, Glasgow, UK; Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
Alexei VazquezCancer Research UK Beatson Institute, Glasgow, UK.
Cancer Research UK Scotland Institute · GBUniversity of Glasgow · GB

Funding

Cancer Research UK 17728Cancer Research UK 18274Cancer Research UK 18278Cancer Research UK 19702Cancer Research UK 21140
6 · The paper itself

Abstract

Serine catabolism to glycine and a one-carbon unit has been linked to the anabolic requirements of proliferating mammalian cells. However, genome-scale modeling predicts a catabolic role with one-carbon release as formate. We experimentally prove that in cultured cancer cells and nontransformed fibroblasts, most of the serine-derived one-carbon units are released from cells as formate, and that formate release is dependent on mitochondrial reverse 10-CHO-THF synthetase activity. We also show that in cancer cells, formate release is coupled to mitochondrial complex I activity, whereas in nontransformed fibroblasts, it is partially insensitive to inhibition of complex I activity. We demonstrate that in mice, about 50% of plasma formate is derived from serine and that serine starvation or complex I inhibition reduces formate synthesis in vivo. These observations transform our understanding of one-carbon metabolism and have implications for the treatment of diabetes and cancer with complex I inhibitors.

Indexed as

folate metabolismmetforminmitochondria metabolismone-carbon metabolismoverflow metabolismSerine metabolism

Identifiers

PMID27819051
PMCPMC5091358
OpenAlexW2539462439

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.