Evidence map›Paper›PMID 36035756›Full record

ArticleMolecular therapy. Nucleic acids2022

miR-199a-3p increases the anti-tumor activity of palbociclib in liver cancer models.

Elisa Callegari, Paola Guerriero, Cristian Bassi, Lucilla D'Abundo, Antonio Frassoldati, Edi Simoni, Laura Astolfi, Enrico Maria Silini, Silvia Sabbioni, Massimo Negrini

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2022. 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 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
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  4. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Elisa CallegariDepartment of Translational Medicine, University of Ferrara, Via Luigi Borsari, 44121 Ferrara, Italy.
Paola GuerrieroDepartment of Translational Medicine, University of Ferrara, Via Luigi Borsari, 44121 Ferrara, Italy.
Cristian BassiDepartment of Translational Medicine, University of Ferrara, Via Luigi Borsari, 44121 Ferrara, Italy.
Lucilla D'AbundoDepartment of Translational Medicine, University of Ferrara, Via Luigi Borsari, 44121 Ferrara, Italy.
Antonio FrassoldatiDepartment of Translational Medicine, University of Ferrara, Via Luigi Borsari, 44121 Ferrara, Italy.
Edi SimoniBioacoustics Research Laboratory, Department of Neurosciences, University of Padua, 35129 Padua, Italy.
Laura AstolfiBioacoustics Research Laboratory, Department of Neurosciences, University of Padua, 35129 Padua, Italy.
Enrico Maria SiliniSection of Anatomy and Pathology, University Hospital of Parma, 43121 Parma, Italy.
Silvia SabbioniLaboratorio Per Le Tecnologie Delle Terapie Avanzate (LTTA), Department of Translational Medicine, University of Ferrara, 44121 Ferrara, Italy.
Massimo NegriniDepartment of Translational Medicine, University of Ferrara, Via Luigi Borsari, 44121 Ferrara, Italy.
University of Ferrara · ITUniversity of Padua · ITUniversity of Parma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Palbociclib is in early-stage clinical testing in advanced hepatocellular carcinoma (HCC). Here, we investigated whether the anti-tumor activity of palbociclib, which prevents the CDK4/6-mediated phosphorylation of RB1 but simultaneously activates AKT signaling, could be improved by its combination with a PI3K/AKT/mTOR inhibitor in liver cancer models. The selective pan-AKT inhibitor, MK-2206, or the microRNA-199a-3p were tested in combination with palbociclib in HCC cell lines and in the TG221 HCC transgenic mouse model. The combination palbociclib/MK-2206 was highly effective, but too toxic to be tolerated by mice. Conversely, the combination miR-199a-3p mimics/palbociclib not only induced a complete or partial regression of tumor lesions, but was also well tolerated. After 3 weeks of treatment, the combination produced a significant reduction in number and size of tumor nodules in comparison with palbociclib or miR-199a-3p mimics used as single agents. Moreover, we also reported the efficacy of this combination against sorafenib-resistant cells

Indexed as

anti-tumor therapyHCCmir-199a-3pMK-2206Oligonucleotides: Therapies and Applicationspalbociclibsorafenib resistance

Identifiers

PMID36035756
PMCPMC9395755
OpenAlexW4286255934

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.