Evidence map›Paper›PMID 36722641›Full record

ArticleEMBO molecular medicine2023

Mutated axon guidance gene PLXNB2 sustains growth and invasiveness of stem cells isolated from cancers of unknown primary.

Serena Brundu, Virginia Napolitano, Giulia Franzolin, Ettore Lo Cascio, Roberta Mastrantonio, Gabriele Sardo, Eliano Cascardi, Federica Verginelli, Sergio Sarnataro, Gennaro Gambardella and 6 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Multi-stage mechanisms of tumor metastasis and therapeutic strategies.Signal transduction and targeted therapy · 2024
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  3. Article
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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

16 authors at 4 institutions in 1 country.

Serena Brundu *Candiolo Cancer Institute, FPO-IRCCS, Turin, Italy.ORCID 0000-0003-4468-7492
Virginia Napolitano *Department of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0002-3869-519X
Giulia Franzolin *Candiolo Cancer Institute, FPO-IRCCS, Turin, Italy.ORCID 0000-0002-5271-1977
Ettore Lo CascioDepartment of Biotechnological Sciences and Intensive Care, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0003-2597-5624
Roberta MastrantonioDepartment of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0002-1764-457X
Gabriele SardoCandiolo Cancer Institute, FPO-IRCCS, Turin, Italy.
Eliano CascardiCandiolo Cancer Institute, FPO-IRCCS, Turin, Italy.ORCID 0000-0003-1287-4285
Federica VerginelliCandiolo Cancer Institute, FPO-IRCCS, Turin, Italy.ORCID 0000-0002-8762-8815
Sergio SarnataroTelethon Institute of Genetic and Medicine, Pozzuoli, Italy.ORCID 0000-0002-6001-9892
Gennaro GambardellaTelethon Institute of Genetic and Medicine, Pozzuoli, Italy.ORCID 0000-0001-7517-1347
Alberto PisacaneCandiolo Cancer Institute, FPO-IRCCS, Turin, Italy.
Alessandro ArcovitoDepartment of Biotechnological Sciences and Intensive Care, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0002-8384-4844
Carla BoccaccioCandiolo Cancer Institute, FPO-IRCCS, Turin, Italy.ORCID 0000-0003-2620-9083
Paolo M ComoglioIFOM, FIRC Institute of Molecular Oncology, Milan, Italy.ORCID 0000-0002-7056-5328
Enrico Giraudo *Candiolo Cancer Institute, FPO-IRCCS, Turin, Italy.ORCID 0000-0003-4128-4786
Luca Tamagnone *Department of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0002-2884-7946
Candiolo Cancer Institute · ITUniversità Cattolica del Sacro Cuore · ITTelethon Institute Of Genetics And Medicine · ITIFOM · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genetic changes sustaining the development of cancers of unknown primary (CUP) remain elusive. The whole-exome genomic profiling of 14 rigorously selected CUP samples did not reveal specific recurring mutation in known driver genes. However, by comparing the mutational landscape of CUPs with that of most other human tumor types, it emerged a consistent enrichment of changes in genes belonging to the axon guidance KEGG pathway. In particular, G842C mutation of PlexinB2 (PlxnB2) was predicted to be activating. Indeed, knocking down the mutated, but not the wild-type, PlxnB2 in CUP stem cells resulted in the impairment of self-renewal and proliferation in culture, as well as tumorigenic capacity in mice. Conversely, the genetic transfer of G842C-PlxnB2 was sufficient to promote CUP stem cell proliferation and tumorigenesis in mice. Notably, G842C-PlxnB2 expression in CUP cells was associated with basal EGFR phosphorylation, and EGFR blockade impaired the viability of CUP cells reliant on the mutated receptor. Moreover, the mutated PlxnB2 elicited CUP cell invasiveness, blocked by EGFR inhibitor treatment. In sum, we found that a novel activating mutation of the axon guidance gene PLXNB2 sustains proliferative autonomy and confers invasive properties to stem cells isolated from cancers of unknown primary, in EGFR-dependent manner.

Indexed as

Neoplasms, Unknown PrimaryNeoplastic Stem CellsNerve Tissue ProteinsAnimalsAxon GuidanceErbB ReceptorsHumansMiceMutationNeoplasm Recurrence, LocalErbB ReceptorsNerve Tissue ProteinsPLXNB2 protein, humanPlxnb2 protein, mouseCUPEGFRexomemutationPlexin

Identifiers

PMID36722641
PMCPMC9994481
OpenAlexW4318754369

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.