Evidence map›Paper›PMID 35045283›Full record

ArticleCell reports2022

Lineage-specific silencing of PSAT1 induces serine auxotrophy and sensitivity to dietary serine starvation in luminal breast tumors.

Bo-Hyun Choi, Vipin Rawat, Jenny Högström, Philippa A Burns, Kelly O Conger, Mete Emir Ozgurses, Jaymin M Patel, Tejas S Mehta, Angelica Warren, Laura M Selfors and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Regulation of PSAT1 and PHGDH by m6A in endocrine-resistant breast cancer cells.Biochimica et biophysica acta. Molecular basis of disease · 2026
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  9. mNature communications · 2025
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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

12 authors at 4 institutions in 1 country.

Bo-Hyun ChoiDepartment of Physiology and Biophysics, University of Illinois College of Medicine, 835 South Wolcott Avenue, Room E202 M/C 901, Chicago, IL 60612, USA; University of Illinois Cancer Center, Chicago, IL 60612, USA.
Vipin RawatDepartment of Physiology and Biophysics, University of Illinois College of Medicine, 835 South Wolcott Avenue, Room E202 M/C 901, Chicago, IL 60612, USA; University of Illinois Cancer Center, Chicago, IL 60612, USA.
Jenny HögströmBeth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Philippa A BurnsDepartment of Physiology and Biophysics, University of Illinois College of Medicine, 835 South Wolcott Avenue, Room E202 M/C 901, Chicago, IL 60612, USA; University of Illinois Cancer Center, Chicago, IL 60612, USA.
Kelly O CongerDepartment of Physiology and Biophysics, University of Illinois College of Medicine, 835 South Wolcott Avenue, Room E202 M/C 901, Chicago, IL 60612, USA; University of Illinois Cancer Center, Chicago, IL 60612, USA.
Mete Emir OzgursesDepartment of Physiology and Biophysics, University of Illinois College of Medicine, 835 South Wolcott Avenue, Room E202 M/C 901, Chicago, IL 60612, USA; University of Illinois Cancer Center, Chicago, IL 60612, USA.
Jaymin M PatelBeth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Tejas S MehtaDepartment of Radiology, UMass Memorial Medical Center, Worcester, MA 01655, USA.
Angelica WarrenBeth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Laura M SelforsDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Taru MuranenBeth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Jonathan L ColoffDepartment of Physiology and Biophysics, University of Illinois College of Medicine, 835 South Wolcott Avenue, Room E202 M/C 901, Chicago, IL 60612, USA; University of Illinois Cancer Center, Chicago, IL 60612, USA. Electronic address: coloff@uic.edu.
University of Illinois Urbana-Champaign · USBeth Israel Deaconess Medical Center · USHarvard University · USUMass Memorial Health Care · US

Funding

Targeting Serine Auxotrophy in Luminal Breast CancerR37CA251216 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Jonathan L. Coloff · 2021 to 2026
$2.1M
Mechanisms of extracellular matrix mediated drug resistanceR00CA180221 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI MURANEN, TARU ELIISA · 2016 to 2018
$747k
Identifying Proliferation-Independent Metabolic Vulnerabilities in CancerK22CA215828 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI COLOFF, JONATHAN L. · 2018 to 2020
$564k
NCI NIH HHS K22 CA215828NCI NIH HHS R00 CA180221NCI NIH HHS R37 CA251216
6 · The paper itself

Abstract

A major challenge of targeting metabolism for cancer therapy is pathway redundancy, in which multiple sources of critical nutrients can limit the effectiveness of some metabolism-targeted therapies. Here, we analyze lineage-dependent gene expression in human breast tumors to identify differences in metabolic gene expression that may limit pathway redundancy and create therapeutic vulnerabilities. We find that the serine synthesis pathway gene PSAT1 is the most depleted metabolic gene in luminal breast tumors relative to basal tumors. Low PSAT1 prevents de novo serine biosynthesis and sensitizes luminal breast cancer cells to serine and glycine starvation in vitro and in vivo. This PSAT1 expression disparity preexists in the putative cells of origin of basal and luminal tumors and is due to luminal-specific hypermethylation of the PSAT1 gene. Our data demonstrate that luminal breast tumors are auxotrophic for serine and may be uniquely sensitive to therapies targeting serine availability.

Indexed as

Breast NeoplasmsFemaleHumansSerineTransaminasesphosphoserine aminotransferaseSerineTransaminasesauxotrophybreast cancerdietluminal tumorsPHGDHPSAT1serinetumor metabolism

Identifiers

PMID35045283
PMCPMC8845302
OpenAlexW4226046608

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.