Evidence map›Paper›PMID 38997257›Full record

ArticleNature communications2024

Glucose-6-phosphate dehydrogenase maintains redox homeostasis and biosynthesis in LKB1-deficient KRAS-driven lung cancer.

Taijin Lan, Sara Arastu, Jarrick Lam, Hyungsin Kim, Wenping Wang, Samuel Wang, Vrushank Bhatt, Eduardo Cararo Lopes, Zhixian Hu, Michael Sun and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

36 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. Disulfidptosis: molecular mechanisms and therapeutic targets.Signal transduction and targeted therapy · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Taijin LanRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.
Sara ArastuRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.
Jarrick LamRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.
Hyungsin KimRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.
Wenping WangRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.
Samuel WangRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.ORCID 0000-0001-7089-4597
Vrushank BhattRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.
Eduardo Cararo LopesRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.ORCID 0000-0002-5316-5146
Zhixian HuRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.
Michael SunRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.
Xuefei LuoRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.
Jonathan M GhergurovichDepartment of Molecular Biology, Princeton University, Princeton, NJ, 08544, USA.ORCID 0000-0002-6565-2275
Xiaoyang SuRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.ORCID 0000-0001-8081-1396
Joshua D RabinowitzRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.ORCID 0000-0002-1247-4727
Eileen WhiteRutgers Cancer Institute, New Brunswick, NJ, 08901, USA.ORCID 0000-0003-2961-3065
Jessie Yanxiang GuoRutgers Cancer Institute, New Brunswick, NJ, 08901, USA. yanxiang@cinj.rutgers.edu.ORCID 0000-0001-9212-7954

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Tracie Saunders · 1997 to 2026
$94.5M
Tumor cell metabolism in actionR01CA163591 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI JOSHUA D RABINOWITZ, Eileen P. White · 2012 to 2026
$7.0M
Elucidate the mechanism of autophagy in supporting Lkb1-deficient lung tumorigenesis and metastasisR01CA237347 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI GUO, YANXIANG · 2020 to 2025
$1.8M
Targeting autophagy to increase the sensitivity of LKB1-deficient lung tumors to angiogenesis inhibitorR21CA263136 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI GUO, YANXIANG · 2022 to 2023
$400k
American Cancer Society (American Cancer Society, Inc.) ACS 134036-RSG-19-165-01-TBGFoundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.) R01CA163591Foundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.) R01CA237347Foundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.) R21CA263136NCI NIH HHS P30 CA072720NCI NIH HHS R01 CA163591NCI NIH HHS R01 CA237347NCI NIH HHS R21 CA263136
6 · The paper itself

Abstract

Cancer cells depend on nicotinamide adenine dinucleotide phosphate (NADPH) to combat oxidative stress and support reductive biosynthesis. One major NADPH production route is the oxidative pentose phosphate pathway (committed step: glucose-6-phosphate dehydrogenase, G6PD). Alternatives exist and can compensate in some tumors. Here, using genetically-engineered lung cancer mouse models, we show that G6PD ablation significantly suppresses Kras

Indexed as

Glucosephosphate DehydrogenaseHomeostasisLung NeoplasmsNADPOxidation-ReductionProtein Serine-Threonine KinasesProto-Oncogene Proteins p21(ras)AMP-Activated Protein Kinase KinasesAMP-Activated Protein KinasesAnimalsCell Line, TumorFemaleHumansLipogenesisMaleMiceAMP-Activated Protein Kinase KinasesAMP-Activated Protein KinasesGlucosephosphate DehydrogenaseHras protein, mouseKRAS protein, humanNADPProtein Serine-Threonine KinasesProto-Oncogene Proteins p21(ras)STK11 protein, humanStk11 protein, mouseTumor Suppressor Protein p53

Identifiers

PMID38997257
PMCPMC11245543

What Socratic 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 Socratic graph.