Evidence map›Paper›PMID 22174856›Full record

ArticlePloS one2011

MicroRNA expression characterizes oligometastasis(es).

Yves A Lussier, H Rosie Xing, Joseph K Salama, Nikolai N Khodarev, Yong Huang, Qingbei Zhang, Sajid A Khan, Xinan Yang, Michael D Hasselle, Thomas E Darga and 10 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 122 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
122citing papers in PubMed, 3 pooled it
5.0field-weighted citation impact, top 5% 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.

NCT03457467 phase2unknown statusnot on this mapstarted 2018, after this paper: background citation

Clinical Study of Apatinib Mesylate Combined With Stereotactic Body Radiation Therapy in the Treatment of Oligometastasis of Breast Cancer

TypeinterventionalSponsorYan LiRan2018 to 2020Enrolled30ConditionsBreast CancerArmsApatinib, SBRT
NCT04758481 naunknown statusnot on this mapstarted 2021, after this paper: background citation

Consolidation Conventional Radiotherapy + Stereotactic Body Radiotherapy of All Body Locations With the Disease at 3 Months After First Line Chemotherapy in Stage IV Oligometastatic Non-small Cell Lung Cancer, Prior to Maintenance Therapy

TypeinterventionalSponsorUniversity Hospital OstravaRan2021 to 2023Enrolled20ConditionsNon-small Cell Lung CancerArmsprimary tumour radiotherapy, stereotactic body radiotherapy, maintenance radiotherapy
3 · Its place in the literature

Who cites it

122 citing papers in PubMed, 3 syntheses or guidelines pooled it, 277 citations in OpenAlex.

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62 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

20 authors at 2 institutions in 1 country.

Yves A LussierComprehensive Cancer Center, University of Chicago, Chicago, Illinois, United States of America. ylussier@uic.edu
H Rosie Xing
Joseph K Salama
Nikolai N Khodarev
Yong Huang
Qingbei Zhang
Sajid A Khan
Xinan Yang
Michael D Hasselle
Thomas E Darga
Renuka Malik
Hanli Fan
Samantha Perakis
Matthew Filippo
Kimberly Corbin
Younghee Lee
Mitchell C Posner
Steven J Chmura
Samuel Hellman
Ralph R Weichselbaum
University of Chicago · USDuke Medical Center · US

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI MARK W. LINGEN · 1985 to 2026
$122.1M
Nation Center: Multi-Scale Study- Cellular Networks(RMI)U54CA121852 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2005 to 2015
$37.4M
TRANSLATIONAL RESEARCH UNIVERSITY OF CHICAGO: CLINICAL TRIALSUL1RR024999 · NCRR · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2007 to 2011
$25.3M
Semantic Approaches to Phenotypic Databases AnalysesK22LM008308 · NLM · UNIVERSITY OF CHICAGO · PI LUSSIER, YVES A · 2004 to 2006
$468k
NCI NIH HHS 5P30CA014599-35NCI NIH HHS 5U54CA121852-5NCI NIH HHS P30 CA014599NCI NIH HHS U54 CA121852NCRR NIH HHS 5UL1RR024999-04NCRR NIH HHS UL1 RR024999NLM NIH HHS K22 LM008308NLM NIH HHS K22 LM008308-04
6 · The paper itself

Abstract

backgroundCancer staging and treatment presumes a division into localized or metastatic disease. We proposed an intermediate state defined by ≤ 5 cumulative metastasis(es), termed oligometastases. In contrast to widespread polymetastases, oligometastatic patients may benefit from metastasis-directed local treatments. However, many patients who initially present with oligometastases progress to polymetastases. Predictors of progression could improve patient selection for metastasis-directed therapy.

methodsHere, we identified patterns of microRNA expression of tumor samples from oligometastatic patients treated with high-dose radiotherapy.

resultsPatients who failed to develop polymetastases are characterized by unique prioritized features of a microRNA classifier that includes the microRNA-200 family. We created an oligometastatic-polymetastatic xenograft model in which the patient-derived microRNAs discriminated between the two metastatic outcomes. MicroRNA-200c enhancement in an oligometastatic cell line resulted in polymetastatic progression.

conclusionsThese results demonstrate a biological basis for oligometastases and a potential for using microRNA expression to identify patients most likely to remain oligometastatic after metastasis-directed treatment.

Indexed as

AnimalsCell Line, TumorCluster AnalysisDatabases, GeneticDisease Models, AnimalDisease ProgressionFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansLungMiceMicroRNAsNeoplasm MetastasisReproducibility of ResultsXenograft Model Antitumor AssaysMicroRNAs

Identifiers

PMID22174856
PMCPMC3236765
OpenAlexW2090749716

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.