Evidence map›Paper›PMID 35184157›Full record

ArticleOncogene2022

TSPAN6 is a suppressor of Ras-driven cancer.

Patrick O Humbert, Tamara Zoranovic Pryjda, Blanka Pranjic, Andrew Farrell, Kohei Fujikura, Ricardo de Matos Simoes, Rezaul Karim, Ivona Kozieradzki, Shane J F Cronin, G Gregory Neely and 4 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Oncogene, 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 4 countries.

Patrick O HumbertDepartment of Biochemistry & Genetics, School of Molecular Sciences, La Trobe University, Bundoora, VIC, 3086, Australia. P.Humbert@latrobe.edu.au.ORCID http://orcid.org/0000-0002-1366-6691
Tamara Zoranovic Pryjda *Institute of Molecular Biotechnology of the Austrian Academy of Science, Dr. Bohrgasse 3, 1030, Vienna, Austria.ORCID http://orcid.org/0000-0002-5369-6385
Blanka Pranjic *Institute of Molecular Biotechnology of the Austrian Academy of Science, Dr. Bohrgasse 3, 1030, Vienna, Austria.
Andrew FarrellDepartment of Biochemistry & Genetics, School of Molecular Sciences, La Trobe University, Bundoora, VIC, 3086, Australia.
Kohei FujikuraDepartment of Medical Genetics, Life Sciences Institute, University of British Columbia, Vancouver, BC, Canada.
Ricardo de Matos SimoesCenter for Integrative Bioinformatics Vienna, Max F. Perusetz Laboratories, Dr.-Bohr-Gasse 9/6, A-1030, Vienna, Austria.
Rezaul KarimInstitute of Molecular Biotechnology of the Austrian Academy of Science, Dr. Bohrgasse 3, 1030, Vienna, Austria.
Ivona KozieradzkiInstitute of Molecular Biotechnology of the Austrian Academy of Science, Dr. Bohrgasse 3, 1030, Vienna, Austria.
Shane J F CroninInstitute of Molecular Biotechnology of the Austrian Academy of Science, Dr. Bohrgasse 3, 1030, Vienna, Austria.
G Gregory NeelyInstitute of Molecular Biotechnology of the Austrian Academy of Science, Dr. Bohrgasse 3, 1030, Vienna, Austria.ORCID http://orcid.org/0000-0002-1957-9732
Thomas F MeyerMax Planck Institute for Infection Biology, Charite Platz 1, 10117, Berlin, Germany.ORCID http://orcid.org/0000-0002-6120-8679
Astrid HagelkruysInstitute of Molecular Biotechnology of the Austrian Academy of Science, Dr. Bohrgasse 3, 1030, Vienna, Austria.ORCID http://orcid.org/0000-0003-3015-4038
Helena E RichardsonDepartment of Biochemistry & Genetics, School of Molecular Sciences, La Trobe University, Bundoora, VIC, 3086, Australia. H.Richardson@latrobe.edu.au.ORCID http://orcid.org/0000-0003-3852-4953
Josef M PenningerInstitute of Molecular Biotechnology of the Austrian Academy of Science, Dr. Bohrgasse 3, 1030, Vienna, Austria. josef.penninger@ubc.ca.ORCID http://orcid.org/0000-0002-8194-3777
Institute of Molecular Biotechnology · ATLa Trobe University · AUAustrian Academy of Sciences · ATChristian-Albrechts-Universität zu Kiel · DEMax Perutz Labs · ATUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oncogenic mutations in the small GTPase RAS contribute to ~30% of human cancers. In a Drosophila genetic screen, we identified novel and evolutionary conserved cancer genes that affect Ras-driven tumorigenesis and metastasis in Drosophila including confirmation of the tetraspanin Tsp29Fb. However, it was not known whether the mammalian Tsp29Fb orthologue, TSPAN6, has any role in RAS-driven human epithelial tumors. Here we show that TSPAN6 suppressed tumor growth and metastatic dissemination of human RAS activating mutant pancreatic cancer xenografts. Whole-body knockout as well as tumor cell autonomous inactivation using floxed alleles of Tspan6 in mice enhanced Kras

Indexed as

OncogenesPancreatic NeoplasmsTetraspaninsAnimalsCarcinogenesisCell Line, TumorCell Transformation, NeoplasticGenes, rasHumansMammalsMiceMutationProto-Oncogene Proteins p21(ras)Proto-Oncogene Proteins p21(ras)TetraspaninsTSPAN6 protein, human

Identifiers

PMID35184157
PMCPMC8975741
OpenAlexW4213055357

What OpenQuestion holds

Textmetadata
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.