Evidence map›Paper›PMID 29278877›Full record

ArticleCancer biomarkers : section A of Disease markers2018

Deregulation of sialidases in human normal and tumor tissues.

Matilde Forcella, Alessandra Mozzi, Federico M Stefanini, Alice Riva, Samantha Epistolio, Francesca Molinari, Elisabetta Merlo, Eugenio Monti, Paola Fusi, Milo Frattini

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Degradation System: Sialidase.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
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  6. Review
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  12. Targeting Aberrant Sialylation to Treat Cancer.Medicines (Basel, Switzerland) · 2019
    Article
  13. Article
  14. Exploration of the Sialic Acid World.Advances in carbohydrate chemistry and biochemistry · 2018
    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

10 authors at 4 institutions in 2 countries.

Matilde ForcellaDepartment of Biotechnologies and Biosciences, University of Milano-Bicocca, Milan, Italy.
Alessandra MozziDepartment of Biotechnologies and Biosciences, University of Milano-Bicocca, Milan, Italy.
Federico M StefaniniDepartment of Statistics, Computer Science, Applications, University of Florence, Florence, Italy.
Alice RivaInstitute of Pathology, Locarno, Switzerland.
Samantha EpistolioInstitute of Pathology, Locarno, Switzerland.
Francesca MolinariInstitute of Pathology, Locarno, Switzerland.
Elisabetta MerloInstitute of Pathology, Locarno, Switzerland.
Eugenio MontiDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Paola FusiDepartment of Biotechnologies and Biosciences, University of Milano-Bicocca, Milan, Italy.
Milo FrattiniInstitute of Pathology, Locarno, Switzerland.
Istituto Cantonale di Patologia · CHUniversity of Milano-Bicocca · ITUniversity of Brescia · ITUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAberrant sialylation is a characteristic feature associated with cancer. The four types of mammalian sialidases identified to date have been shown to behave in different manners during carcinogenesis. While NEU1, NEU2 and NEU4 have been observed to oppose malignant phenotypes, the membrane-bound sialidase NEU3 was revealed to promote cancer progression.

objectivesWith the aim of improving the knowledge about sialidases deregulation in various cancer types, we investigated the amount of NEU1, NEU3 and NEU4 transcripts in paired normal and tumor tissues from 170 patients with 11 cancer types.

methodsmRNA was extracted from patients' tissue specimens and retrotranscribed into cDNA, which was quantified by Real-Time PCR.

resultsWe found NEU1 and NEU3 to be up regulated, while NEU4 was down regulated in most cancer types. In particular, colorectal cancer tissues showed the highest increase in NEU3 expression. Both NEU1 and NEU3 showed a strong up-regulation in ovarian cancer.

conclusionsOur data show that human sialidases are expressed at different levels in healthy tissues and are strongly deregulated in tumors. Moreover, sialidases expression in our European cohort showed significant differences from Asian populations. Some of these peculiar features open potential applications of sialidases in cancer diagnosis and therapy.

Indexed as

Gene Expression Regulation, NeoplasticAgedAged, 80 and overCase-Control StudiesFemaleHumansMaleMiddle AgedMultigene FamilyNeoplasmsNeuraminidaseProtein IsoformsNeuraminidaseProtein Isoformscancer progressiondiagnosis and therapysialidase expressionSialome

Identifiers

PMID29278877
PMCPMC13078297
OpenAlexW2779394557

What OpenQuestion holds

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Registered trials

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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.