Evidence map›Paper›PMID 25142144›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2014

A three-microRNA signature predicts responses to platinum-based doublet chemotherapy in patients with lung adenocarcinoma.

Motonobu Saito, Kouya Shiraishi, Kenji Matsumoto, Aaron J Schetter, Hiroko Ogata-Kawata, Naoto Tsuchiya, Hideo Kunitoh, Hiroshi Nokihara, Shun-Ichi Watanabe, Koji Tsuta and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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  5. An Insight into miR-1290: An Oncogenic miRNA with Diagnostic Potential.International journal of molecular sciences · 2022
    Review
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  8. miR-608 and miR-4513 significantly contribute to the prognosis of lung adenocarcinoma treated with EGFR-TKIs.Laboratory investigation; a journal of technical methods and pathology · 2019
    Article
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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

15 authors at 8 institutions in 4 countries.

Motonobu SaitoDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan. Department of Organ Regulatory Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kouya ShiraishiDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.
Kenji MatsumotoDepartment of Allergy and Immunology, National Research Institute for Child Health and Development, Setagaya, Tokyo, Japan.
Aaron J SchetterLaboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
Hiroko Ogata-KawataDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.
Naoto TsuchiyaDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.
Hideo KunitohDepartment of Medical Oncology, Japanese Red Cross Medical Center, National Cancer Center Hospital, Tokyo, Japan.
Hiroshi NokiharaDivision of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Shun-Ichi WatanabeDivision of Thoracic Surgery, National Cancer Center Hospital, Tokyo, Japan.
Koji TsutaDivision of Pathology and Clinical Laboratories, National Cancer Center Hospital, Tokyo, Japan.
Kensuke KumamotoDepartment of Organ Regulatory Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.
Seiichi TakenoshitaDepartment of Organ Regulatory Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.
Jun YokotaDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan. Cancer Genome Biology, Institute of Predictive and Personalized Medicine of Cancer, Barcelona, Spain.
Curtis C HarrisLaboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
Takashi KohnoDivision of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan. tkkohno@ncc.go.jp.
National Cancer Research Institute · GBFukushima Medical University · JPNational Cancer Center · USNational Cancer Institute · USInstitute of Predictive and Personalized Medicine of Cancer · ESJapanese Red Cross Medical Center · JPNational Cancer Center Hospital East · JPNational Center For Child Health and Development · JP

Funding

Precision Medicine of CancerZIABC011492 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HARRIS, CURTIS · 2013 to 2025
$23.2M
Molecular Epidemiology of Human Lung CancerZ01BC005480 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HARRIS, CURTIS · 1996 to 2008
$2.3M
Intramural NIH HHS Z01 BC005480
6 · The paper itself

Abstract

purposeTo examine the clinical utility of intratumor microRNAs (miRNA) as a biomarker for predicting responses to platinum-based doublet chemotherapy in patients with recurring lung adenocarcinoma (LADC). EXPERIMENTAL

designThe expression of miRNAs was examined in LADC tissues surgically resected from patients treated with platinum-based doublet chemotherapy at the time of LADC recurrence. Microarray-based screening of 904 miRNAs followed by quantitative reverse transcription-PCR-based verification in 40 test cohort samples, including 16 (40.0%) responders, was performed to identify miRNAs that are differentially expressed in chemotherapy responders and nonresponders. Differential expression was confirmed in a validation cohort (n = 63 samples), including 18 (28.6%) responders. An miRNA signature that predicted responses to platinum-based doublet chemotherapy was identified and its accuracy was examined by principal component and support vector machine analyses. Genotype data for the TP53-Arg72Pro polymorphism, which is associated with responses to platinum-based doublet chemotherapy, were subsequently incorporated into the prediction analysis.

resultsA signature comprising three miRNAs (miR1290, miR196b, and miR135a*) enabled the prediction of a chemotherapeutic response (rather than progression-free and overall survival) with high accuracy in both the test and validation cohorts (82.5% and 77.8%). Examination of the latter was performed using miRNAs extracted from archived formalin-fixed paraffin-embedded tissues. Combining this miRNA signature with the TP53-Arg72Pro polymorphism genotype marginally improved the predictive power.

conclusionThe three-miRNA signature in surgically resected primary LADC tissues may by clinically useful for predicting responsiveness to platinum-based doublet chemotherapy in patients with LADC recurrence.

Indexed as

AdenocarcinomaAdenocarcinoma of LungAdultAgedAntineoplastic AgentsArea Under CurveBiomarkers, TumorFemaleHumansLung NeoplasmsMaleMicroRNAsMiddle AgedOligonucleotide Array Sequence AnalysisPlatinum CompoundsReverse Transcriptase Polymerase Chain ReactionAntineoplastic AgentsBiomarkers, TumorMicroRNAsMIRN1290 microRNA, humanMIRN135 microRNA, humanMIRN196 microRNA, humanPlatinum Compounds

Identifiers

PMID25142144
PMCPMC6329384
OpenAlexW2107988985

What OpenQuestion holds

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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.