Evidence map›Paper›PMID 38073374›Full record

ArticleCancer biomarkers : section A of Disease markers2024

Circulating miR-10b, soluble urokinase-type plasminogen activator receptor, and plasminogen activator inhibitor-1 as predictors of non-small cell lung cancer progression and treatment response.

Lyana Setiawan, Rahajuningsih Setiabudy, Siti Boedina Kresno, Noorwati Sutandyo, Elisna Syahruddin, Frederica Jovianti, Siti Nadliroh, Sofia Mubarika, Rianto Setiabudy, Nurjati C Siregar

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Article in Cancer biomarkers : section A of Disease markers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

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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 at 3 institutions in 1 country.

Lyana SetiawanDepartment of Clinical Pathology, Dharmais National Cancer Center, Jakarta, Indonesia.
Rahajuningsih SetiabudyDepartment of Clinical Pathology, Faculty of Medicine, University of Indonesia, Jakarta, Indonesia.
Siti Boedina KresnoDepartment of Clinical Pathology, Dharmais National Cancer Center, Jakarta, Indonesia.
Noorwati SutandyoDepartment of Hematology and Medical Oncology, Dharmais National Cancer Center, Jakarta, Indonesia.
Elisna SyahruddinDepartment of Pulmonology, Faculty of Medicine, University of Indonesia/Persahabatan General Hospital, Jakarta, Indonesia.
Frederica JoviantiDharmais National Cancer Center, Jakarta, Indonesia.
Siti NadlirohDharmais National Cancer Center, Jakarta, Indonesia.
Sofia MubarikaDepartment of Histology, Faculty of Medicine, Gadjah Mada University, Yogyakarta, Indonesia.
Rianto SetiabudyDepartment of Pharmacology, Faculty of Medicine, University of Indonesia, Jakarta, Indonesia.
Nurjati C SiregarDepartment of Anatomical Pathology, Faculty of Medicine, University of Indonesia/Cipto Mangunkusumo Hospital, Jakarta, Indonesia.
Dharmais Cancer Hospital · IDUniversity of Indonesia · IDUniversitas Gadjah Mada · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite advances in lung cancer treatment, most lung cancers are diagnosed at an advanced stage. Expression of microRNA10b (miR-10b) and fibrinolytic activity, as reflected by soluble urokinase-type plasminogen activator receptor (suPAR) and plasminogen activator inhibitor 1 (PAI-1), are promising biomarker candidates.

objectiveTo assess the expression of miR-10b, and serum levels of suPAR and PAI-1 in advanced stage non-small cell lung cancer (NSCLC) patients, and their correlation with progression, treatment response and prognosis.

methodsThe present prospective cohort and survival study was conducted at Dharmais National Cancer Hospital and included advanced stage NSCLC patients diagnosed between March 2015 and September 2016. Expression of miR-10b was quantified using qRT-PCR. Levels of suPAR and PAI-1 were assayed using ELISA. Treatment response was evaluated using the RECIST 1.1 criteria. Patients were followed up until death or at least 1 year after treatment.

resultsAmong the 40 patients enrolled, 25 completed at least four cycles of chemotherapy and 15 patients died during treatment. Absolute miR-10b expression ⩾ 592,145 copies/μL or miR-10b fold change ⩾ 0.066 were protective for progressive disease and poor treatment response, whereas suPAR levels ⩾ 4,237 pg/mL was a risk factor for progressive disease and poor response. PAI-1 levels > 4.6 ng/mL was a protective factor for poor response. Multivariate analysis revealed suPAR as an independent risk factor for progression (ORa⁢d⁢j, 13.265; 95% confidence intervals (CI), 2.26577.701; P= 0.006) and poor response (ORa⁢d⁢j, 15.609; 95% CI, 2.221-109.704; P= 0.006), whereas PAI-1 was an independent protective factor of poor response (ORa⁢d⁢j, 0.127; 95% CI, 0.019-0.843; P= 0.033).

conclusionsSince miR-10b cannot be used as an independent risk factor for NSCLC progression and treatment response, we developed a model to predict progression using suPAR levels and treatment response using suPAR and PAI-1 levels. Further studies are needed to validate this model.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsMicroRNAsHumansPlasminogen Activator Inhibitor 1Prospective StudiesReceptors, Urokinase Plasminogen ActivatorMicroRNAsMIRN10 microRNA, humanPlasminogen Activator Inhibitor 1PLAUR protein, humanReceptors, Urokinase Plasminogen ActivatorSERPINE1 protein, humanmiR-10bnon-small cell lung cancerplasminogen activator inhibitor 1 (PAI-1)soluble urokinase-type plasminogen activator receptor (suPAR)

Identifiers

PMID38073374
PMCPMC11002724
OpenAlexW4389399942

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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.