Evidence map›Paper›PMID 28716985›Full record

ArticleJournal of investigative medicine : the official publication of the American Federation for Clinical Research2017

Two microRNA signatures for malignancy and immune infiltration predict overall survival in advanced epithelial ovarian cancer.

Ilya Korsunsky, Janaki Parameswaran, Iuliana Shapira, John Lovecchio, Andrew Menzin, Jill Whyte, Lisa Dos Santos, Sharon Liang, Tawfiqul Bhuiya, Mary Keogh and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of investigative medicine : the official publication of the American Federation for Clinical Research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

12 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Article
  6. Review
  7. Regulation of PD-1/PD-L1 Pathway in Cancer by Noncoding RNAs.Pathology oncology research : POR · 2020
    Review
  8. Article
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  12. Review
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

16 authors at 5 institutions in 1 country.

Ilya KorsunskyGenomics and Human Genetics, Feinstein Institute for Medical Research, Manhasset, New York, USA.
Janaki ParameswaranYale University School of Medicine, New Haven, Connecticut, USA.
Iuliana ShapiraSUNY Downstate Medical Center College of Medicine, Hematology/Oncology, Brooklyn, New York, USA.
John LovecchioNorthwell Health, Great Neck, New York, USA.
Andrew MenzinNorthwell Health, Great Neck, New York, USA.
Jill WhyteNorthwell Health, Great Neck, New York, USA.
Lisa Dos SantosNorthwell Health, Great Neck, New York, USA.
Sharon LiangNorthwell Health, Great Neck, New York, USA.
Tawfiqul BhuiyaNorthwell Health, Great Neck, New York, USA.
Mary KeoghGenomics and Human Genetics, Feinstein Institute for Medical Research, Manhasset, New York, USA.
Houman KhaliliGenomics and Human Genetics, Feinstein Institute for Medical Research, Manhasset, New York, USA.
Cassandra PondGenomics and Human Genetics, Feinstein Institute for Medical Research, Manhasset, New York, USA.
Anthony LiewGenomics and Human Genetics, Feinstein Institute for Medical Research, Manhasset, New York, USA.
Andrew ShihGenomics and Human Genetics, Feinstein Institute for Medical Research, Manhasset, New York, USA.
Peter K GregersenGenomics and Human Genetics, Feinstein Institute for Medical Research, Manhasset, New York, USA.
Annette T LeeGenomics and Human Genetics, Feinstein Institute for Medical Research, Manhasset, New York, USA.
Feinstein Institute for Medical Research · USNorthwell Health · USHofstra University · USSUNY Downstate Health Sciences University · USYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs have been established as key regulators of tumor gene expression and as prime biomarker candidates for clinical phenotypes in epithelial ovarian cancer (EOC). We analyzed the coexpression and regulatory structure of microRNAs and their co-localized gene targets in primary tumor tissue of 20 patients with advanced EOC in order to construct a regulatory signature for clinical prognosis. We performed an integrative analysis to identify two prognostic microRNA/mRNA coexpression modules, each enriched for consistent biological functions. One module, enriched for malignancy-related functions, was found to be upregulated in malignant versus benign samples. The second module, enriched for immune-related functions, was strongly correlated with imputed intratumoral immune infiltrates of T cells, natural killer cells, cytotoxic lymphocytes, and macrophages. We validated the prognostic relevance of the immunological module microRNAs in the publicly available The Cancer Genome Atlas data set. These findings provide novel functional roles for microRNAs in the progression of advanced EOC and possible prognostic signatures for survival.

Indexed as

Gene Expression ProfilingGene Expression Regulation, NeoplasticAdultAgedAged, 80 and overCarcinoma, Ovarian EpithelialDemographyFemaleHumansKiller Cells, NaturalMacrophagesMicroRNAsMiddle AgedNeoplasms, Glandular and EpithelialNeoplasm StagingOvarian NeoplasmsMicroRNAsRNA, MessengerBiological MarkersBiostatisticsCancerClinical ResearchOvarian Neoplasms

Identifiers

PMID28716985
PMCPMC5847100
OpenAlexW2734654479

What OpenQuestion holds

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LicenceCC BY-NC
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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.