Evidence map›Paper›PMID 34075699›Full record

ArticleMolecular oncology2021

MicroRNA expression profiling with a droplet digital PCR assay enables molecular diagnosis and prognosis of cancers of unknown primary.

Noemi Laprovitera, Mattia Riefolo, Elisa Porcellini, Giorgio Durante, Ingrid Garajova, Francesco Vasuri, Ariane Aigelsreiter, Nadia Dandachi, Giuseppe Benvenuto, Federico Agostinis and 8 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
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  6. MicroRNAs in neurodegenerative diseases: from molecular mechanisms to clinical biomarkers, detection methods and therapeutic strategies-advances and challenges.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
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  11. Synergic activity of FGFR2 and MEK inhibitors in the treatment of FGFR2-amplified cancers of unknown primary.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
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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

18 authors at 8 institutions in 3 countries.

Noemi LaproviteraDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Italy.ORCID 0000-0002-2737-4665
Mattia RiefoloDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Italy.
Elisa PorcelliniDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Italy.
Giorgio DuranteDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Italy.
Ingrid GarajovaMedical Oncology Unit, University Hospital of Parma, Italy.
Francesco VasuriPathology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Italy.
Ariane AigelsreiterDiagnostic and Research Institute of Pathology, Medical University of Graz, Austria.
Nadia DandachiDivision of Oncology, Medical University of Graz, Austria.ORCID 0000-0001-9093-0743
Giuseppe BenvenutoDepartment of Biology, University of Padua, Italy.
Federico AgostinisDepartment of Biology, University of Padua, Italy.
Silvia SabbioniDepartment of Life Sciences and Biotechnologies, University of Ferrara, Italy.
Ioana Berindan NeagoeResearch Center for Functional Genomics, Biomedicine and Translational Medicine, "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Chiara RomualdiDepartment of Biology, University of Padua, Italy.
Andrea ArdizzoniDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Italy.
Davide TrerèDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Italy.
Martin PichlerDivision of Oncology, Medical University of Graz, Austria.
Antonietta D'ErricoDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Italy.
Manuela FerracinDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Italy.ORCID 0000-0002-1595-6887
Azienda USL di Bologna · ITUniversity of Bologna · ITUniversity of Padua · ITUniversity of Ferrara · ITUniversity of Graz · ATIuliu Hațieganu University of Medicine and Pharmacy · ROMedical University of Graz · ATUniversity of Parma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastasis is responsible for the majority of cancer-related deaths. Particularly, challenging is the management of metastatic cancer of unknown primary site (CUP), whose tissue of origin (TOO) remains undetermined even after extensive investigations and whose therapy is rather unspecific and poorly effective. Molecular approaches to identify the most probable TOO of CUPs can overcome some of these issues. In this study, we applied a predetermined set of 89 microRNAs (miRNAs) to infer the TOO of 53 metastatic cancers of unknown or uncertain origin. The miRNA expression was assessed with droplet digital PCR in 159 samples, including primary tumors from 17 tumor classes (reference set) and metastases of known and unknown origin (test set). We combined two different statistical models for class prediction to obtain the most probable TOOs: the nearest shrunken centroids approach of Prediction Analysis of Microarrays (PAMR) and the least absolute shrinkage and selection operator (LASSO) models. The molecular test was successful for all formalin-fixed paraffin-embedded samples and provided a TOO identification within 1 week from the biopsy procedure. The most frequently predicted origins were gastrointestinal, pancreas, breast, lung, and bile duct. The assay was applied also to multiple metastases from the same CUP, collected from different metastatic sites: The predictions showed a strong agreement, intrinsically validating our assay. The final CUPs' TOO prediction was compared with the clinicopathological hypothesis of primary site. Moreover, a panel of 13 miRNAs proved to have prognostic value and be associated with overall survival in CUP patients. Our study demonstrated that miRNA expression profiling in CUP samples could be employed as diagnostic and prognostic test. Our molecular analysis can be performed on request, concomitantly with standard diagnostic workup and in association with genetic profiling, to offer valuable indications about the possible primary site, thereby supporting treatment decisions.

Indexed as

MicroRNAsNeoplasms, Unknown PrimaryGene Expression ProfilingGene Expression Regulation, NeoplasticHumansPolymerase Chain ReactionMicroRNAscancer of unknown primarydroplet digital PCRmetastasismicroRNAsmolecular diagnostics

Identifiers

PMID34075699
PMCPMC8486570
OpenAlexW3165383988

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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.