Evidence map›Paper›PMID 29282901›Full record

ArticleCancer medicine2018

AKT3 drives adenoid cystic carcinoma development in salivary glands.

Katalin Zboray, Julian Mohrherr, Patricia Stiedl, Klemens Pranz, Laura Wandruszka, Beatrice Grabner, Robert Eferl, Richard Moriggl, Dagmar Stoiber, Kazuhito Sakamoto and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 19 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

14 authors at 5 institutions in 2 countries.

Katalin ZborayLudwig Boltzmann Institute for Cancer Research (LBI-CR), Vienna, Austria.
Julian MohrherrLudwig Boltzmann Institute for Cancer Research (LBI-CR), Vienna, Austria.
Patricia StiedlLudwig Boltzmann Institute for Cancer Research (LBI-CR), Vienna, Austria.
Klemens PranzLudwig Boltzmann Institute for Cancer Research (LBI-CR), Vienna, Austria.
Laura WandruszkaLudwig Boltzmann Institute for Cancer Research (LBI-CR), Vienna, Austria.
Beatrice GrabnerLudwig Boltzmann Institute for Cancer Research (LBI-CR), Vienna, Austria.
Robert EferlInstitute of Cancer Research, Medical University of Vienna, Comprehensive Cancer Center (CCC), Vienna, Austria.ORCID 0000-0002-6074-7144
Richard MorigglLudwig Boltzmann Institute for Cancer Research (LBI-CR), Vienna, Austria.
Dagmar StoiberLudwig Boltzmann Institute for Cancer Research (LBI-CR), Vienna, Austria.
Kazuhito SakamotoEppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska.
Kay-Uwe WagnerEppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska.
Helmut PopperInstitute of Pathology, Research Unit Molecular Lung and Pleura Pathology, Medical University of Graz, Graz, 8036, Austria.
Emilio CasanovaLudwig Boltzmann Institute for Cancer Research (LBI-CR), Vienna, Austria.ORCID 0000-0001-7992-5361
Herwig P MollDepartment of Physiology, Center of Physiology and Pharmacology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-6438-9068
Ludwig Boltzmann Institute for Cancer Research · ATComprehensive Cancer Center Vienna · ATNebraska Medical Center · USMedical University of Graz · ATUniversity of Veterinary Medicine Vienna · AT

Funding

Growth-Regulatory Signaling Networks in Breast CancerR01CA117930 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WAGNER, KAY-UWE · 2006 to 2016
$2.5M
NCI NIH HHS R01 CA117930
6 · The paper itself

Abstract

Salivary gland cancer is an aggressive and painful cancer, but a rare tumor type accounting for only ~0.5% of cancer cases. Tumors of the salivary gland exhibit heterogeneous histologic and genetic features and they are subdivided into different subtypes, with adenoid cystic carcinomas (ACC) being one of the most abundant. Treatment of ACC patients is afflicted by high recurrence rates, the high potential of the tumors to metastasize, as well as the poor response of ACC to chemotherapy. A prerequisite for the development of targeted therapies is insightful genetic information for driver core cancer pathways. Here, we developed a transgenic mouse model toward establishment of a preclinical model. There is currently no available mouse model for adenoid cystic carcinomas as a rare disease entity to serve as a test system to block salivary gland tumors with targeted therapy. Based on tumor genomic data of ACC patients, a key role for the activation of the PI3K-AKT-mTOR pathway was suggested in tumors of secretory glands. Therefore, we investigated the role of Akt3 expression in tumorigenesis and report that Akt3 overexpression results in ACC of salivary glands with 100% penetrance, while abrogation of transgenic Akt3 expression could revert the phenotype. In summary, our findings validate a novel mouse model to study ACC and highlight the druggable potential of AKT3 in the treatment of salivary gland patients.

Indexed as

AnimalsAnti-Bacterial AgentsCarcinoma, Adenoid CysticDoxycyclineHumansMiceMice, TransgenicPrognosisProto-Oncogene Proteins c-aktSalivary Gland NeoplasmsAnti-Bacterial AgentsDoxycyclineProto-Oncogene Proteins c-aktAdenoid cystic carcinomaAKT3MMTV-tTA mouse modeloncogene addictionsalivary gland cancer

Identifiers

PMID29282901
PMCPMC5806106
OpenAlexW2780555702

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.