Evidence map›Paper›PMID 31878932›Full record

ReviewCell communication and signaling : CCS2019

Hedgehog/GLI signaling in tumor immunity - new therapeutic opportunities and clinical implications.

Sandra Grund-Gröschke, Georg Stockmaier, Fritz Aberger

Open access · goldAbstract readReview
In one paragraph

Review in Cell communication and signaling : CCS, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

44 citing papers in PubMed, 76 citations in OpenAlex.

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  12. Current Status of Hedgehog Signaling Inhibitors.Current topics in medicinal chemistry · 2024
    Review
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  17. The Role of Hedgehog Signaling in the Melanoma Tumor Bone Microenvironment.International journal of molecular sciences · 2023
    Article
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  20. Emerging Roles of Hedgehog Signaling in Cancer Immunity.International journal of molecular sciences · 2023
    Review
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

3 authors at 1 institution in 1 country.

Sandra Grund-GröschkeDepartment of Biosciences, Cancer Cluster Salzburg, University of Salzburg, Hellbrunner Strasse, 34, 5020, Salzburg, Austria.
Georg StockmaierDepartment of Biosciences, Cancer Cluster Salzburg, University of Salzburg, Hellbrunner Strasse, 34, 5020, Salzburg, Austria.
Fritz AbergerDepartment of Biosciences, Cancer Cluster Salzburg, University of Salzburg, Hellbrunner Strasse, 34, 5020, Salzburg, Austria. fritz.aberger@sbg.ac.at.ORCID 0000-0003-2009-6305
University of Salzburg · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Uncontrolled activation of the Hedgehog/Glioma-associated oncogene (HH/GLI) pathway is a potent oncogenic driver signal promoting numerous cancer hallmarks such as proliferation, survival, angiogenesis, metastasis and metabolic rewiring. Several HH pathway inhibitors have already been approved for medical therapy of advanced and metastatic basal cell carcinoma and acute myeloid leukemia with partially impressive therapeutic activity. However, de novo and acquired resistance as well as severe side effects and unexplained lack of therapeutic efficacy are major challenges that urgently call for improved treatment options with more durable responses. The recent breakthroughs in cancer immunotherapy have changed our current understanding of targeted therapy and opened up promising therapeutic opportunities including combinations of selective cancer pathway and immune checkpoint inhibitors. Although HH/GLI signaling has been intensely studied with respect to the classical hallmarks of cancer, its role in the modulation of the anti-tumoral immune response has only become evident in recent studies. These have uncovered HH/GLI regulated immunosuppressive mechanisms such as enhanced regulatory T-cell formation and production of immunosuppressive cytokines. In light of these exciting novel data on oncogenic HH/GLI signaling in immune cross-talk and modulation, we summarize and connect in this review the existing knowledge from different HH-related cancers and chronic inflammatory diseases. This is to provide a basis for the investigation and evaluation of novel treatments combining immunotherapeutic strategies with approved as well as next-generation HH/GLI inhibitors. Further, we also critically discuss recent studies demonstrating a possible negative impact of current HH/GLI pathway inhibitors on the anti-tumoral immune response, which may explain some of the disappointing results of several oncological trials with anti-HH drugs. Additional file 1Video abstract. (9500 kb).

Indexed as

Signal TransductionAnimalsAntineoplastic AgentsCarcinomaHedgehog ProteinsHumansImmunotherapyLeukemia, Myeloid, AcuteZinc Finger Protein GLI1Antineoplastic AgentsHedgehog ProteinsZinc Finger Protein GLI1Cancer immunotherapyChronic inflammationCombination therapyImmune checkpoint inhibitorsImmune evasionImmunosuppressionOncogenic Hedgehog/GLI signalingTumor microenvironment

Identifiers

PMID31878932
PMCPMC6933925
OpenAlexW2998415228

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.