Evidence map›Paper›PMID 32978808›Full record

ArticleHepatology (Baltimore, Md.)2021

DCLK1, a Putative Stem Cell Marker in Human Cholangiocarcinoma.

Lorenzo Nevi, Sabina Di Matteo, Guido Carpino, Ilaria Grazia Zizzari, Safarikia Samira, Valeria Ambrosino, Daniele Costantini, Diletta Overi, Antonella Giancotti, Marco Monti and 17 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 44 citations in OpenAlex.

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  14. Kelch-like proteins in the gastrointestinal tumors.Acta pharmacologica Sinica · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 8 institutions in 3 countries.

Lorenzo Nevi *Department of Biosciences, University of Milan, Milan, Italy.ORCID 0000-0003-0924-2551
Sabina Di Matteo *Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.ORCID 0000-0002-2586-7159
Guido CarpinoDepartment of Movement, Human and Health Sciences, University of Rome "Foro Italico", Rome, Italy.ORCID 0000-0001-8570-2519
Ilaria Grazia ZizzariDepartment of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
Safarikia SamiraDepartment of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
Valeria AmbrosinoDepartment of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
Daniele CostantiniDepartment of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
Diletta OveriDepartment of Anatomical, Histological, Forensic Medicine and Orthopedics Sciences, Sapienza University of Rome, Rome, Italy.ORCID 0000-0003-3561-8903
Antonella GiancottiDepartment of Maternal and Child Health and Urologic Sciences, Umberto I Hospital, Sapienza University of Rome, Rome, Italy.
Marco MontiDepartment of Maternal and Child Health and Urologic Sciences, Umberto I Hospital, Sapienza University of Rome, Rome, Italy.
Daniela BoscoDepartment of Pathological Anatomy and Cytodiagnostic, Sapienza University of Rome, Rome, Italy.
Valerio De PeppoHepatobiliary and Pancreatic Surgery IRCCS, Regina Elena National Cancer Institute, Rome, Italy.
Andrea OddiHepatobiliary and Pancreatic Surgery IRCCS, Regina Elena National Cancer Institute, Rome, Italy.
Agostino Maria De RoseSurgery, Hepatobiliary Unit, Catholic University of the Sacred Heart School of Medicine and Surgery, Rome, Italy.
Fabio MelandroDepartment of General Surgery and Organ Transplantation, Sapienza University of Rome, Rome, Italy.
Maria Consiglia BragazziDepartment of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Rome, Italy.
Jessica FaccioliDepartment of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Rome, Italy.
Sara MassironiDivision of Gastroenterology and Center for Autoimmune Liver Diseases, Department of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy.
Gian Luca GraziHepatobiliary and Pancreatic Surgery IRCCS, Regina Elena National Cancer Institute, Rome, Italy.
Pierluigi Benedetti PaniciDepartment of Maternal and Child Health and Urologic Sciences, Umberto I Hospital, Sapienza University of Rome, Rome, Italy.
Paquale Bartomeo BerlocoDepartment of General Surgery and Organ Transplantation, Sapienza University of Rome, Rome, Italy.
Felice GiulianteSurgery, Hepatobiliary Unit, Catholic University of the Sacred Heart School of Medicine and Surgery, Rome, Italy.
Vincenzo CardinaleDepartment of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Rome, Italy.
Pietro InvernizziDivision of Gastroenterology and Center for Autoimmune Liver Diseases, Department of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy.ORCID 0000-0003-3262-1998
Giuseppina CarettiDepartment of Biosciences, University of Milan, Milan, Italy.
Eugenio GaudioDepartment of Anatomical, Histological, Forensic Medicine and Orthopedics Sciences, Sapienza University of Rome, Rome, Italy.
Domenico AlvaroDepartment of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
Sapienza University of Rome · ITNational Cancer Institute · MYPoliclinico Umberto I · ITAzienda Ospedaliera San Gerardo · ITUniversità Cattolica del Sacro Cuore · ITUniversity of Milan · ITBambino Gesù Children's Hospital · ITForo Italico University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsCholangiocarcinoma (CCA) is a very aggressive cancer showing the presence of high cancer stem cells (CSCs). Doublecortin-like kinase1 (DCLK1) has been demonstrated as a CSC marker in different gastroenterological solid tumors. Our aim was to evaluate in vitro the expression and the biological function of DCLK1 in intrahepatic CCA (iCCA) and perihilar CCA (pCCA). APPROACH AND

resultsSpecimens surgically resected of human CCA were enzymatically digested, submitted to immunosorting for specific CSC markers (LGR5 [leucine-rich repeat-containing G protein-coupled receptor], CD [clusters of differentiation] 90, EpCAM [epithelial cell adhesion molecule], CD133, and CD13), and primary cell cultures were prepared. DCLK1 expression was analyzed in CCA cell cultures by real-time quantitative PCR, western blot, and immunofluorescence. Functional studies have been performed by evaluating the effects of selective DCLK1 inhibitor (LRRK2-IN-1) on cell proliferation (MTS [3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium] assay, cell population doubling time), apoptosis, and colony formation capacity. DCLK1 was investigated in situ by immunohistochemistry and real-time quantitative PCR. DCLK1 serum concentration was analyzed by enzyme-linked immunosorbent assay. We describe DCLK1 in CCA with an increased gene and protein DCLK1 expression in pCCA

conclusionsDCLK1 characterizes a specific CSC subpopulation of iCCA

Indexed as

Bile Duct NeoplasmsBiomarkers, TumorCell Line, TumorCell ProliferationCholangiocarcinomaDoublecortin-Like KinasesGene Expression Regulation, NeoplasticHumansIntracellular Signaling Peptides and ProteinsNeoplastic Stem CellsProtein Serine-Threonine KinasesReceptors, G-Protein-CoupledBiomarkers, TumorDCLK1 protein, humanDoublecortin-Like KinasesIntracellular Signaling Peptides and ProteinsLGR5 protein, humanProtein Serine-Threonine KinasesReceptors, G-Protein-Coupled

Identifiers

PMID32978808
PMCPMC8243252
OpenAlexW3088664811

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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.