Evidence map›Paper›PMID 32984844›Full record

ArticleNature cancer2020

eIF5B drives integrated stress response-dependent translation of PD-L1 in lung cancer.

Shruthy Suresh, BeiBei Chen, Jingfei Zhu, Ryan J Golden, Changzheng Lu, Bret M Evers, Nicole Novaresi, Bethany Smith, Xiaowei Zhan, Vanessa Schmid and 15 more

Open access · greenAbstract read
In one paragraph

Article in Nature cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
6.5field-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

76 citing papers in PubMed, 122 citations in OpenAlex.

  1. ClonalLife science alliance · 2026
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16 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

25 authors at 4 institutions in 1 country.

Shruthy SureshDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-2985-8284
BeiBei ChenQuantitative Biomedical Research Center, UT Southwestern Medical Center, Dallas, TX, USA.
Jingfei ZhuDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, USA.
Ryan J GoldenDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0003-3988-0730
Changzheng LuDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX, United States.
Bret M EversDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX, United States.ORCID http://orcid.org/0000-0001-5686-0315
Nicole NovaresiDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, USA.
Bethany SmithDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, USA.
Xiaowei ZhanDepartment of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX, USA.
Vanessa SchmidEugene McDermott Center for Human Growth and Development, UT Southwestern Medical Center, Dallas, TX, USA.
Sojeong JunChildren's Research Institute, UT Southwestern Medical Center, Dallas, TX, USA.
Chelsea M KaraczDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX, United States.
Michael PeytonHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Lin ZhongDepartment of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX, USA.
Zhuoyu WenDepartment of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX, USA.
Adwait Amod SatheEugene McDermott Center for Human Growth and Development, UT Southwestern Medical Center, Dallas, TX, USA.
Chao XingDepartment of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-1838-0502
Carmen BehrensDepartment of Thoracic Head and Neck Medical Oncology, MD Anderson Cancer Center, Houston, TX, USA.
Ignacio I WistubaDepartment of Thoracic Head and Neck Medical Oncology, MD Anderson Cancer Center, Houston, TX, USA.
Guanghua XiaoDepartment of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX, USA.
Yang XieQuantitative Biomedical Research Center, UT Southwestern Medical Center, Dallas, TX, USA.
Yang-Xin FuDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX, United States.ORCID http://orcid.org/0000-0001-8441-6617
John D MinnaHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Joshua T MendellDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0001-8479-2284
Kathryn A O'DonnellDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, USA. Kathryn.ODonnell@UTSouthwestern.edu.ORCID http://orcid.org/0000-0003-2215-1064
Southwestern Medical Center · USThe University of Texas MD Anderson Cancer Center · USHoward Hughes Medical Institute · USThe University of Texas Southwestern Medical Center · US

Funding

UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HEYMACH, JOHN V., MINNA, JOHN D. · 1996 to 2024
$57.4M
UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MELANIE H. COBB · 2010 to 2026
$53.7M
University of Texas Southwestern Medical Center SPORE in Kidney CancerP50CA196516 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI James Brugarolas · 2016 to 2026
$24.7M
The intersection of RNA biology and tumor biologyR35CA197311 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MENDELL, JOSHUA T · 2015 to 2021
$5.1M
The role of PCDH7 in lung cancer pathogenesisR01CA207763 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI O'DONNELL, KATHRYN ANN · 2017 to 2021
$2.0M
The role of translation initiation factor eIF5B in lung cancer pathogenesisR01CA273585 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Kathryn Ann O'Donnell · 2023 to 2026
$1.9M
Mechanisms of Disease & Translational ScienceT32GM109776 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI YIN, HELEN L · 2014 to 2018
$573k
Howard Hughes Medical Institute 56006776NCI NIH HHS P30 CA142543NCI NIH HHS P50 CA070907NCI NIH HHS P50 CA196516NCI NIH HHS R01 CA207763NCI NIH HHS R01 CA273585NCI NIH HHS R35 CA197311NIGMS NIH HHS T32 GM109776
6 · The paper itself

Abstract

Cancer cells express high levels of PD-L1, a ligand of the PD-1 receptor on T cells, allowing tumors to suppress T cell activity. Clinical trials utilizing antibodies that disrupt the PD-1/PD-L1 checkpoint have yielded remarkable results, with anti-PD-1 immunotherapy approved as first-line therapy for lung cancer patients. We used CRISPR-based screening to identify regulators of PD-L1 in human lung cancer cells, revealing potent induction of PD-L1 upon disruption of heme biosynthesis. Impairment of heme production activates the integrated stress response (ISR), allowing bypass of inhibitory upstream open reading frames in the

Indexed as

B7-H1 AntigenEukaryotic Initiation FactorsLung NeoplasmsHemeHumansB7-H1 Antigeneukaryotic initiation factor-5BEukaryotic Initiation FactorsHeme

Identifiers

PMID32984844
PMCPMC7511089
OpenAlexW3017360104

What OpenQuestion holds

Textmetadata
LicenceTDM
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.