Evidence map›Paper›PMID 33821796›Full record

ArticleeLife2021

An NKX2-1/ERK/WNT feedback loop modulates gastric identity and response to targeted therapy in lung adenocarcinoma.

Rediet Zewdu, Elnaz Mirzaei Mehrabad, Kelley Ingram, Pengshu Fang, Katherine L Gillis, Soledad A Camolotto, Grace Orstad, Alex Jones, Michelle C Mendoza, Benjamin T Spike and 1 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
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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

11 authors at 1 institution in 1 country.

Rediet ZewduHuntsman Cancer Institute, Salt Lake City, United States.ORCID 0000-0001-6784-6068
Elnaz Mirzaei MehrabadHuntsman Cancer Institute, Salt Lake City, United States.
Kelley IngramHuntsman Cancer Institute, Salt Lake City, United States.
Pengshu FangHuntsman Cancer Institute, Salt Lake City, United States.
Katherine L GillisHuntsman Cancer Institute, Salt Lake City, United States.
Soledad A CamolottoHuntsman Cancer Institute, Salt Lake City, United States.
Grace OrstadHuntsman Cancer Institute, Salt Lake City, United States.
Alex JonesHuntsman Cancer Institute, Salt Lake City, United States.
Michelle C MendozaHuntsman Cancer Institute, Salt Lake City, United States.ORCID 0000-0002-6490-1794
Benjamin T SpikeHuntsman Cancer Institute, Salt Lake City, United States.
Eric L SnyderHuntsman Cancer Institute, Salt Lake City, United States.ORCID 0000-0003-3591-3195
University of Utah · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI KATHARINE S ULLMAN · 1986 to 2026
$72.6M
DEVELOPMENTAL BIOLOGY TRAINING PROGRAMT32HD007491 · NICHD · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI James Alan Gagnon, Kristen M Kwan · 1995 to 2026
$8.0M
Transcriptional Regulation of Lung Cancer IdentityR01CA212415 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Eric Lee Snyder · 2017 to 2026
$3.2M
Patho-Genetic Analysis of Invasive Mucinous Adenocarcinoma of the LungR01CA240317 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI MAEDA, YUTAKA, SNYDER, ERIC LEE · 2020 to 2024
$3.1M
Univ of Utah Cell Sorter for Flow Cytometry CoreS10RR026802 · NCRR · UNIVERSITY OF UTAH · PI GREEN, WAYNE FRANCIS · 2010 to 2010
$500k
Epigenetic regulation of NKX2-1-negative lung adenocarcinoma cellular identity by FoxA1 and FoxA2F31CA275266 · NCI · UNIVERSITY OF UTAH · PI GILLIS, KATHERINE L · 2022 to 2023
$90k
Characterizing the role of FOXA1 and FOXA2 in NKX2-1 positive lung adenocarcinomaF31CA243427 · NCI · UNIVERSITY OF UTAH · PI ORSTAD, GRACE · 2020 to 2022
$74k
NCI NIH HHS F31 CA243427NCI NIH HHS F31 CA275266NCI NIH HHS P30 CA042014NCI NIH HHS R01 CA212415NCI NIH HHS R01 CA240317NCRR NIH HHS S10 RR026802NICHD NIH HHS T32 HD007491
6 · The paper itself

Abstract

Cancer cells undergo lineage switching during natural progression and in response to therapy. NKX2-1 loss in human and murine lung adenocarcinoma leads to invasive mucinous adenocarcinoma (IMA), a lung cancer subtype that exhibits gastric differentiation and harbors a distinct spectrum of driver oncogenes. In murine BRAF

Indexed as

Adenocarcinoma of LungAnimalsAnimals, Genetically ModifiedAntineoplastic AgentsCell DifferentiationCell LineageCell Line, TumorCell ProliferationExtracellular Signal-Regulated MAP KinasesFeedback, PhysiologicalHumansLung NeoplasmsMiceMice, 129 StrainMice, Inbred C57BLMice, Inbred NODAntineoplastic AgentsBraf protein, mouseExtracellular Signal-Regulated MAP KinasesMitogen-Activated Protein Kinase KinasesNkx2-1 protein, mouseProtein Kinase InhibitorsProto-Oncogene Proteins B-rafThyroid Nuclear Factor 1Wnt Proteinscancer biologydevelopmental biologyERKhumanlineage switchinglung adenocarcinomamouseNKX2-1targeted therapy

Identifiers

PMID33821796
PMCPMC8102067
OpenAlexW3147966162

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.