Evidence map›Paper›PMID 33670268›Full record

ReviewInternational journal of molecular sciences2021

Targeting Akt in Hepatocellular Carcinoma and Its Tumor Microenvironment.

Mariam Mroweh, Gaël Roth, Thomas Decaens, Patrice N Marche, Hervé Lerat, Zuzana Macek Jílková

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

6 authors at 1 institution in 2 countries.

Mariam MrowehInstitute for Advanced Biosciences, Research Center Inserm U 1209/CNRS 5309, 38700 La Tronche, France.
Gaël RothInstitute for Advanced Biosciences, Research Center Inserm U 1209/CNRS 5309, 38700 La Tronche, France.ORCID 0000-0001-5822-4320
Thomas DecaensInstitute for Advanced Biosciences, Research Center Inserm U 1209/CNRS 5309, 38700 La Tronche, France.ORCID 0000-0003-0928-0048
Patrice N MarcheInstitute for Advanced Biosciences, Research Center Inserm U 1209/CNRS 5309, 38700 La Tronche, France.ORCID 0000-0002-8930-9340
Hervé LeratInstitute for Advanced Biosciences, Research Center Inserm U 1209/CNRS 5309, 38700 La Tronche, France.ORCID 0000-0002-8505-378X
Zuzana Macek JílkováInstitute for Advanced Biosciences, Research Center Inserm U 1209/CNRS 5309, 38700 La Tronche, France.ORCID 0000-0002-2553-5971
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is one of the most common causes of cancer-related deaths worldwide, and its incidence is rising. HCC develops almost exclusively on the background of chronic liver inflammation, which can be caused by chronic alcohol consumption, viral hepatitis, or an unhealthy diet. The key role of chronic inflammation in the process of hepatocarcinogenesis, including in the deregulation of innate and adaptive immune responses, has been demonstrated. The inhibition of Akt (also known as Protein Kinase B) directly affects cancer cells, but this therapeutic strategy also exhibits indirect anti-tumor activity mediated by the modulation of the tumor microenvironment, as demonstrated by using Akt inhibitors AZD5363, MK-2206, or ARQ 092. Moreover, the isoforms of Akt converge and diverge in their designated roles, but the currently available Akt inhibitors fail to display an isoform specificity. Thus, selective Akt inhibition needs to be better explored in the context of HCC and its possible combination with immunotherapy. This review presents a compact overview of the current knowledge concerning the role of Akt in HCC and the effect of Akt inhibition on the HCC and liver tumor microenvironment.

Indexed as

Drug Delivery SystemsTumor MicroenvironmentAminopyridinesCarcinoma, HepatocellularHeterocyclic Compounds, 3-RingHumansImidazolesLiver NeoplasmsProtein Kinase InhibitorsProto-Oncogene Proteins c-aktPyrimidinesPyrrolesAminopyridinescapivasertibHeterocyclic Compounds, 3-RingImidazolesMiransertibMK 2206Protein Kinase InhibitorsProto-Oncogene Proteins c-aktPyrimidinesPyrrolesAKTHCCimmune cellstumor microenvironment

Identifiers

PMID33670268
PMCPMC7917860
OpenAlexW3128231101

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.