Evidence map›Paper›PMID 28634901›Full record

ArticleCellular oncology (Dordrecht, Netherlands)2017

Changes in plasma miR-9, miR-16, miR-205 and miR-486 levels after non-small cell lung cancer resection.

Maria Sromek, Maciej Glogowski, Magdalena Chechlinska, Mariusz Kulinczak, Lukasz Szafron, Klara Zakrzewska, Joanna Owczarek, Piotr Wisniewski, Robert Wlodarczyk, Lukasz Talarek and 2 more

Abstract read
In one paragraph

Article in Cellular oncology (Dordrecht, Netherlands), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

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

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  12. Noncoding RNome as Enabling Biomarkers for Precision Health.International journal of molecular sciences · 2022
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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.

Maria SromekDepartment of Immunology, Maria Sklodowska-Curie Institute - Oncology Centre, Roentgen 5, 02-781, Warsaw, Poland.
Maciej GlogowskiDepartment of Lung Cancer and Chest Tumors, Maria Sklodowska-Curie Institute - Oncology Centre, Roentgen 5, 02-781, Warsaw, Poland.
Magdalena ChechlinskaDepartment of Immunology, Maria Sklodowska-Curie Institute - Oncology Centre, Roentgen 5, 02-781, Warsaw, Poland.
Mariusz KulinczakDepartment of Immunology, Maria Sklodowska-Curie Institute - Oncology Centre, Roentgen 5, 02-781, Warsaw, Poland.
Lukasz SzafronDepartment of Pathology and Laboratory Diagnostics, Maria Sklodowska-Curie Institute - Oncology Centre, Roentgen 5, 02-781, Warsaw, Poland.
Klara ZakrzewskaDepartment of Pathology and Laboratory Diagnostics, Maria Sklodowska-Curie Institute - Oncology Centre, Roentgen 5, 02-781, Warsaw, Poland.
Joanna OwczarekDepartment of Pathology and Laboratory Diagnostics, Maria Sklodowska-Curie Institute - Oncology Centre, Roentgen 5, 02-781, Warsaw, Poland.
Piotr WisniewskiDepartment of Pathology and Laboratory Diagnostics, Maria Sklodowska-Curie Institute - Oncology Centre, Roentgen 5, 02-781, Warsaw, Poland.
Robert WlodarczykDepartment of Lung Cancer and Chest Tumors, Maria Sklodowska-Curie Institute - Oncology Centre, Roentgen 5, 02-781, Warsaw, Poland.
Lukasz TalarekDepartment of Lung Cancer and Chest Tumors, Maria Sklodowska-Curie Institute - Oncology Centre, Roentgen 5, 02-781, Warsaw, Poland.
Maciej TurskiDepartment of Lung Cancer and Chest Tumors, Maria Sklodowska-Curie Institute - Oncology Centre, Roentgen 5, 02-781, Warsaw, Poland.
Jan Konrad SiwickiDepartment of Immunology, Maria Sklodowska-Curie Institute - Oncology Centre, Roentgen 5, 02-781, Warsaw, Poland. jan.siwicki@coi.pl.ORCID http://orcid.org/0000-0002-5083-3022

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe majority of non-small cell lung cancer (NSCLC) patients presents with an advanced-stage disease and, consequently, exhibits a poor overall survival rate. We aimed to assess changes in plasma miR-9, miR-16, miR-205 and miR-486 levels and their potential as biomarkers for the diagnosis and monitoring of NSCLC patients.

methodsPlasma was collected from 50 healthy donors and from NSCLC patients before surgery (n = 61), 1 month after surgery (n = 37) and 1 year after surgery (n = 14). microRNA levels were quantified using qRT-PCR.

resultsWe found in NSCLC patients before treatment, both with squamous cell carcinoma (SQCC) and adenocarcinoma (ADC), significantly higher plasma miR-16 and miR-486 levels than in healthy individuals. Pre-treatment miR-205 concentrations were found to be significantly higher in SQCC than in ADC patients, and only SQCC patients presented significantly higher circulating miR-205 levels than healthy donors. SQCC plasma miR-9 levels were not different from normal control levels, but in ADC they were found to be significantly decreased. A combination of plasma miR-16, miR-205 and miR-486 measurements was found to discriminate NSCLC patients from healthy persons, with a specificity of 95% and a sensitivity of 80%. Following tumor resection, we found that the miR-9 and miR-205 levels significantly decreased, even below the normal level, whereas the increased miR-486 level persisted up to one year after surgery, and the miR-16 level decreased to normal. After tumor resection, none of the miR levels tested was found to relate to recurrence.

conclusionsOur data indicate that miR-9, miR-16, miR-205 and miR-486 may serve as NSCLC biomarkers. The observed cancer-related pre- and post-operative changes in their plasma levels may not only reflect the presence of a primary cancer, but also of a systemic response to cancer.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, Non-Small-Cell LungDiagnosis, DifferentialFemaleGene Expression Regulation, NeoplasticHumansLung NeoplasmsMaleMicroRNAsMiddle AgedTreatment OutcomeBiomarkers, TumorMicroRNAsMIR205, humanMIRN16 microRNA, humanMIRN486 microRNA, humanMIRN92 microRNA, humanCancer biomarkerCirculating microRNANon-small cell lung carcinoma

Identifiers

PMID28634901
PMCPMC13001572

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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.