Evidence map›Paper›PMID 30152518›Full record

ArticleInternational journal of cancer2019

Somatostatin receptor 2 signaling promotes growth and tumor survival in small-cell lung cancer.

Jonathan M Lehman, Megan D Hoeksema, Jeremy Staub, Jun Qian, Bradford Harris, J Clay Callison, Jennifer Miao, Chanjuan Shi, Rosana Eisenberg, Heidi Chen and 2 more

Abstract read
In one paragraph

Article in International journal of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

37 citing papers in PubMed, 55 citations in OpenAlex.

  1. Malignancy Detection Rates of [Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
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  16. Comparison ofRadiology. Imaging cancer · 2025
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  17. Combining [European journal of nuclear medicine and molecular imaging · 2024
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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 3 institutions in 1 country.

Jonathan M LehmanDivision of Medical Oncology, Vanderbilt Ingram Cancer Center, Nashville, TN.ORCID 0000-0001-6349-0332
Megan D HoeksemaDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt Ingram Cancer Center, Nashville, TN.
Jeremy StaubDivision of Medical Oncology, Vanderbilt Ingram Cancer Center, Nashville, TN.
Jun QianDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt Ingram Cancer Center, Nashville, TN.
Bradford HarrisDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt Ingram Cancer Center, Nashville, TN.
J Clay CallisonUniversity of Tennessee Graduate School of Medicine, Tennessee Valley Healthcare System, Nashville Campus, Nashville, TN.
Jennifer MiaoVanderbilt University School of Medicine, Tennessee Valley Healthcare System, Nashville Campus, Nashville, TN.
Chanjuan ShiDepartment of Pathology, Microbiology and Immunology, Tennessee Valley Healthcare System, Nashville Campus, Nashville, TN.
Rosana EisenbergDepartment of Pathology, Microbiology and Immunology, Tennessee Valley Healthcare System, Nashville Campus, Nashville, TN.
Heidi ChenVanderbilt University Department of Biostatistics, Tennessee Valley Healthcare System, Nashville Campus, Nashville, TN.
Sheau-Chiann ChenVanderbilt University Department of Biostatistics, Tennessee Valley Healthcare System, Nashville Campus, Nashville, TN.
Pierre P MassionDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt Ingram Cancer Center, Nashville, TN.
Vanderbilt University · USVA Tennessee Valley Healthcare System · USVanderbilt-Ingram Cancer Center

Funding

TARGETING NOTCH 3 IN LUNG CANCERP50CA090949 · NCI · VANDERBILT UNIVERSITY · PI MASSION, PIERRE P. · 2001 to 2011
$24.1M
Single-Cell Biology and Data Analysis Shared Resource (SCB-DA SR)U54CA217450 · NCI · VANDERBILT UNIVERSITY · PI WEAVER, ALISSA M · 2018 to 2022
$8.5M
Molecular Approaches to Early Detection of Lung CancerR01CA102353 · NCI · VANDERBILT UNIVERSITY · PI MASSION, PIERRE P. · 2005 to 2014
$2.4M
Pannoramic 250 BF Flash Tissue Microarray systemS10OD016355 · OD · VANDERBILT UNIVERSITY · PI BOYD, KELLI L. · 2014 to 2014
$453k
XFe96 AnalyzerS10OD018015 · OD · VANDERBILT UNIVERSITY · PI LANNIGAN, DEBORAH · 2014 to 2014
$200k
Molecular Biomarkers of Small Cell Lung Cancer BehaviourI01CX000242 · VA · VETERANS HEALTH ADMINISTRATION · PI MASSION, PIERRE P. · 2009 to 2013
–
Phenotypic heterogeneity in small cell lung cancer.I01CX001425 · VA · VETERANS HEALTH ADMINISTRATION · PI MASSION, PIERRE P. · 2016 to 2019
–
CSRD VA I01 CX000242CSRD VA I01 CX001425NCI NIH HHS P50 CA090949NCI NIH HHS R01 CA102353NCI NIH HHS U54 CA217450NIH HHS S10 OD016355NIH HHS S10 OD018015
6 · The paper itself

Abstract

Somatostatin receptor 2 (SSTR2) is overexpressed in a majority of neuroendocrine neoplasms, including small-cell lung carcinomas (SCLCs). SSTR2 was previously considered an inhibitory receptor on cell growth, but its agonists had poor clinical responses in multiple clinical trials. The role of this receptor as a potential therapeutic target in lung cancer merits further investigation. We evaluated the expression of SSTR2 in a cohort of 96 primary tumors from patients with SCLC and found 48% expressed SSTR2. Correlation analysis in both CCLE and an SCLC RNAseq cohort confirmed high-level expression and identified an association between NEUROD1 and SSTR2. There was a significant association with SSTR2 expression profile and poor clinical outcome. We tested whether SSTR2 expression might contribute to tumor progression through activation of downstream signaling pathways, using in vitro and in vivo systems and downregulated SSTR2 expression in lung cancer cells by shRNA. SSTR2 downregulation led to increased apoptosis and dramatically decreased tumor growth in vitro and in vivo in multiple cell lines with decreased AMPKα phosphorylation and increased oxidative metabolism. These results demonstrate a role for SSTR2 signaling in SCLC and suggest that SSTR2 is a poor prognostic biomarker in SCLC and potential future therapeutic signaling target.

Indexed as

AMP-Activated Protein KinasesAnimalsApoptosisBasic Helix-Loop-Helix ProteinsBiomarkers, TumorCell Line, TumorCell ProliferationDisease ProgressionDown-RegulationHumansLung NeoplasmsMiceMice, NudeNerve Tissue ProteinsReceptors, SomatostatinRNA, MessengerAMP-Activated Protein KinasesBasic Helix-Loop-Helix ProteinsBiomarkers, TumorNerve Tissue ProteinsNeurogenic differentiation factor 1Receptors, SomatostatinRNA, MessengerSSTR2 protein, humancancer progressionsomatostatinsurvival

Identifiers

PMID30152518
PMCPMC6448409
OpenAlexW2888905384

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.