Evidence map›Paper›PMID 29576613›Full record

ArticleOncogene2018

HOXB7 overexpression in lung cancer is a hallmark of acquired stem-like phenotype.

Simona Monterisi, Pietro Lo Riso, Karin Russo, Giovanni Bertalot, Manuela Vecchi, Giuseppe Testa, Pier Paolo Di Fiore, Fabrizio Bianchi

Abstract read
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In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 43 citations in OpenAlex.

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  15. The vascular nature of lung-resident mesenchymal stem cells.Stem cells translational medicine · 2021
    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

8 authors at 5 institutions in 1 country.

Simona MonterisiMolecular Medicine Program, European Institute of Oncology, 20141, Milan, Italy.
Pietro Lo RisoDepartment of Experimental Oncology, European Institute of Oncology, 20141, Milan, Italy.
Karin RussoIFOM, The FIRC Institute for Molecular Oncology Foundation, 20139, Milan, Italy.
Giovanni BertalotMolecular Medicine Program, European Institute of Oncology, 20141, Milan, Italy.
Manuela VecchiIFOM, The FIRC Institute for Molecular Oncology Foundation, 20139, Milan, Italy.
Giuseppe TestaDepartment of Experimental Oncology, European Institute of Oncology, 20141, Milan, Italy.
Pier Paolo Di FioreMolecular Medicine Program, European Institute of Oncology, 20141, Milan, Italy.ORCID http://orcid.org/0000-0002-2252-0950
Fabrizio BianchiMolecular Medicine Program, European Institute of Oncology, 20141, Milan, Italy. f.bianchi@operapadrepio.it.ORCID http://orcid.org/0000-0001-7412-8638
European Institute of Oncology · ITIFOM · ITUniversity of Milan · ITCasa Sollievo della Sofferenza · ITHumanitas University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HOXB7 is a homeodomain (HOX) transcription factor involved in regional body patterning of invertebrates and vertebrates. We previously identified HOXB7 within a ten-gene prognostic signature for lung adenocarcinoma, where increased expression of HOXB7 was associated with poor prognosis. This raises the question of how HOXB7 overexpression can influence the metastatic behavior of lung adenocarcinoma. Here, we analyzed publicly available microarray and RNA-seq lung cancer expression datasets and found that HOXB7-overexpressing tumors are enriched in gene signatures characterizing adult and embryonic stem cells (SC), and induced pluripotent stem cells (iPSC). Experimentally, we found that HOXB7 upregulates several canonical SC/iPSC markers and sustains the expansion of a subpopulation of cells with SC characteristics, through modulation of LIN28B, an emerging cancer gene and pluripotency factor, which we discovered to be a direct target of HOXB7. We validated this new circuit by showing that HOXB7 enhances reprogramming to iPSC with comparable efficiency to LIN28B or its target c-MYC, which is a canonical reprogramming factor.

Indexed as

Adenocarcinoma of LungCell Line, TumorCell MovementCell ProliferationEmbryonic Stem CellsGene Expression ProfilingGene Expression Regulation, NeoplasticHEK293 CellsHomeodomain ProteinsHumansInduced Pluripotent Stem CellsLung NeoplasmsNeoplastic Stem CellsProto-Oncogene Proteins c-mycRNA-Binding ProteinsRNA InterferenceHomeodomain ProteinsHOXB7 protein, humanLIN28B protein, humanMYC protein, humanProto-Oncogene Proteins c-mycRNA-Binding ProteinsRNA, Small Interfering

Identifiers

PMID29576613
OpenAlexW2794280940

What OpenQuestion holds

Textmetadata
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.