Evidence map›Paper›PMID 40248723›Full record

ArticleTranslational lung cancer research2025

Persistent and novel changes in plasma microRNA profiles in patients with non-small cell lung cancer following tumour resection.

Maria Sromek, Maciej Głogowski, Magdalena Chechlińska, Mariusz Kulińczak, Michalina Zajdel, Natalia Żeber-Lubecka, Aneta Bałabas, Łukasz M Szafron, Maria Kulecka, Jan K Siwicki

Abstract read
In one paragraph

Article in Translational lung cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

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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

3 citing papers in PubMed.

  1. Review
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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

10 authors.

Maria SromekDepartment of Cancer Biology, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID https://orcid.org/0000-0001-8636-5542
Maciej GłogowskiDepartment of Lung Cancer and Chest Tumors, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID https://orcid.org/0000-0002-0850-0566
Magdalena ChechlińskaDepartment of Cancer Biology, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID https://orcid.org/0000-0001-6139-1234
Mariusz KulińczakDepartment of Cancer Biology, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID https://orcid.org/0000-0002-2517-0116
Michalina ZajdelDepartment of Cancer Biology, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID https://orcid.org/0000-0003-1868-6402
Natalia Żeber-LubeckaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID https://orcid.org/0000-0003-4036-3191
Aneta BałabasDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID https://orcid.org/0000-0003-0228-7650
Łukasz M SzafronDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID https://orcid.org/0000-0003-1670-0274
Maria KuleckaDepartment of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID https://orcid.org/0000-0002-9830-8892
Jan K SiwickiDepartment of Cancer Biology, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID https://orcid.org/0000-0002-5083-3022

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Non-small cell lung cancer (NSCLC) accounts for 80% of lung cancers, the leading cause of cancer mortality. microRNAs (miRNA, miR) have emerged as important components of carcinogenesis and promising biomarkers. We aimed to analyse global plasma miRs in NSCLC patients before and at least one year after tumour resection. Methods: Plasma was collected from the peripheral blood of 24 donors without cancer and of NSCLC patients before surgery (n=36) and at least 1 year after surgery (n=12). Next-generation sequencing (NGS)-based miR profiling was performed. Patients were followed-up for 4 to 12 years after surgery to assess disease recurrence. Results: Untreated NSCLC patients exhibited significant changes in plasma miR levels compared to cancer-free donors (48 up- and 17 down-regulated miRs). miR profiles in patients with adenocarcinoma (ADC) (n=18) and squamous cell carcinoma (SCC) significantly differed (16 and 86 miRs up-, and 15 and 16 miRs down-regulated, respectively). A subset of pre-surgery deregulated miRs was found to be associated with recurrence (49 miRs). Six miRs were shown to have independent prognostic value. After tumour resection, some pre-surgery miR alterations returned to control levels (18 miRs), some others persisted (27 miRs), while also novel plasma miR changes emerged (75 miRs) in patients with no clinical evidence of recurrence. Conclusions: Untreated NSCLC patients present deregulated plasma miRs, some of which may have a potential of prognostic markers. After tumour excision plasma miR profiles change, some miR levels normalise, some changes persist and novel miR changes are observed despite no clinical symptoms of recurrence. Plasma miR profiles in NSCLC patients may suggest systemic abnormalities predisposing to lung cancer and/or reflect a systemic response to pre-cancer/dormant cancer cells.

Indexed as

circulating microRNANon-small cell lung cancer (NSCLC)systemictumour resection

Identifiers

PMID40248723
PMCPMC12000959

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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.