Evidence map›Paper›PMID 30038707›Full record

ArticleOncotarget2018

LMO1 functions as an oncogene by regulating TTK expression and correlates with neuroendocrine differentiation of lung cancer.

Liqin Du, Zhenze Zhao, Milind Suraokar, Spencer S Shelton, Xiuye Ma, Tzu-Hung Hsiao, John D Minna, Ignacio Wistuba, Alexander Pertsemlidis

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

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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

9 authors at 6 institutions in 2 countries.

Liqin DuDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, Texas, USA.
Zhenze ZhaoDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, Texas, USA.
Milind SuraokarDepartments of Pathology and Thoracic/Head and Neck Medical Oncology, UT MD Anderson Cancer Center, Houston, Texas, USA.
Spencer S SheltonDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, Texas, USA.
Xiuye MaGreehey Children's Cancer Research Institute, UT Health Science Center at San Antonio, San Antonio, Texas, USA.
Tzu-Hung HsiaoDepartment of Medical Research, Taichung Veterans General Hospital, Taichung, Taiwan.
John D MinnaHamon Center for Therapeutic Oncology Research and Departments of Pharmacology and Internal Medicine, UT Southwestern Medical Center at Dallas, Dallas, Texas, USA.
Ignacio WistubaDepartments of Pathology and Thoracic/Head and Neck Medical Oncology, UT MD Anderson Cancer Center, Houston, Texas, USA.
Alexander PertsemlidisGreehey Children's Cancer Research Institute, UT Health Science Center at San Antonio, San Antonio, Texas, USA.
Texas State University · USThe University of Texas MD Anderson Cancer Center · USSouthwestern Medical CenterTaichung Veterans General Hospital · TWThe University of Texas Health Science Center at Houston · USThe University of Texas Health Science Center at San Antonio · US

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Robin Jean Leach · 1991 to 2026
$59.1M
microRNA regulation of drug sensitivity in non-small cell lung cancerR01CA129632 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI PERTSEMLIDIS, ALEXANDER · 2007 to 2011
$1.6M
NCI NIH HHS P30 CA054174NCI NIH HHS R01 CA129632
6 · The paper itself

Abstract

LMO1 encodes a protein containing a cysteine-rich LIM domain involved in protein-protein interactions. Recent studies have shown that LMO1 functions as an oncogene in several cancer types, including non-small cell lung cancer (NSCLC). However, the function of LMO1 in other histological subtypes of lung cancer, such as small cell lung cancer (SCLC), was not investigated. In analyzing the expression of LMO1 across a panel of lung cell lines, we found that LMO1 expression levels were significantly and dramatically higher in SCLC cells, an aggressive neuroendocrine subtype of lung cancer, relative to NSCLC and normal lung cells. In NSCLC cells, LMO1 mRNA levels were significantly correlated with expression of neuroendocrine differentiation markers. Our

Indexed as

LMO1lung cancerneuroendocrineTTK

Identifiers

PMID30038707
PMCPMC6049873
OpenAlexW2810428242

What OpenQuestion holds

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LicenceCC BY
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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.