Evidence map›Paper›PMID 35008212›Full record

ReviewCancers2021

Cell Death in Hepatocellular Carcinoma: Pathogenesis and Therapeutic Opportunities.

Ester García-Pras, Anabel Fernández-Iglesias, Jordi Gracia-Sancho, Sofía Pérez-Del-Pulgar

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

42 citing papers in PubMed, 58 citations in OpenAlex.

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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

4 authors at 3 institutions in 2 countries.

Ester García-PrasLiver Unit, Hospital Clínic, University of Barcelona, IDIBAPS, CIBERHED, 08036 Barcelona, Spain.ORCID 0000-0002-2920-2306
Anabel Fernández-IglesiasLiver Vascular Biology Research Group, IDIBAPS, CIBEREHD, 08036 Barcelona, Spain.ORCID 0000-0003-2364-6675
Jordi Gracia-SanchoLiver Vascular Biology Research Group, IDIBAPS, CIBEREHD, 08036 Barcelona, Spain.ORCID 0000-0001-7736-4089
Sofía Pérez-Del-PulgarLiver Unit, Hospital Clínic, University of Barcelona, IDIBAPS, CIBERHED, 08036 Barcelona, Spain.ORCID 0000-0002-9890-300X
Hospital Clínic de Barcelona · ESCentro de Investigación Biomédica en Red · ESUniversity of Bern · CH

Funding

Instituto de Salud Carlos III PI19/00036Instituto de Salud Carlos III PI20/00220Secretaria d'Universitats i Recerca del Departament d'Economia i Coneixement 2017-SGR-1753Secretaria d'Universitats i Recerca del Departament d'Economia i Coneixement 2017-SGR-517
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the most prevalent primary liver cancer and the third leading cause of cancer death worldwide. Closely associated with liver inflammation and fibrosis, hepatocyte cell death is a common trigger for acute and chronic liver disease arising from different etiologies, including viral hepatitis, alcohol abuse, and fatty liver. In this review, we discuss the contribution of different types of cell death, including apoptosis, necroptosis, pyroptosis, or autophagy, to the progression of liver disease and the development of HCC. Interestingly, inflammasomes have recently emerged as pivotal innate sensors with a highly pathogenic role in various liver diseases. In this regard, an increased inflammatory response would act as a key element promoting a pro-oncogenic microenvironment that may result not only in tumor growth, but also in the formation of a premetastatic niche. Importantly, nonparenchymal hepatic cells, such as liver sinusoidal endothelial cells, hepatic stellate cells, and hepatic macrophages, play an important role in establishing the tumor microenvironment, stimulating tumorigenesis by paracrine communication through cytokines and/or angiocrine factors. Finally, we update the potential therapeutic options to inhibit tumorigenesis, and we propose different mechanisms to consider in the tumor microenvironment field for HCC resolution.

Indexed as

nonparenchymal cellsprogrammed cell deathstromal componenttumor microenvironment

Identifiers

PMID35008212
PMCPMC8750350
OpenAlexW4200324164

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.