Evidence map›Paper›PMID 35453784›Full record

ReviewBiology2022

Target Therapy for Hepatocellular Carcinoma: Beyond Receptor Tyrosine Kinase Inhibitors and Immune Checkpoint Inhibitors.

Hyunjung Park, Hyerin Park, Jiyeon Baek, Hyuk Moon, Simon Weonsang Ro

Open access · goldAbstract readReview
In one paragraph

Review in Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 14 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

5 authors at 1 institution in 1 country.

Hyunjung ParkDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si 17104, Korea.
Hyerin ParkDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si 17104, Korea.
Jiyeon BaekDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si 17104, Korea.
Hyuk MoonDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si 17104, Korea.ORCID 0000-0002-6252-2571
Simon Weonsang RoDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si 17104, Korea.ORCID 0000-0003-2187-3698
Kyung Hee University · KR

Funding

National Research Foundation of Korea 2019R1A2C2009518
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a major health concern worldwide, and its incidence is increasing steadily. To date, receptor tyrosine kinases (RTKs) are the most favored molecular targets for the treatment of HCC, followed by immune checkpoint regulators such as PD-1, PD-L1, and CTLA-4. With less than desirable clinical outcomes from RTK inhibitors as well as immune checkpoint inhibitors (ICI) so far, novel molecular target therapies have been proposed for HCC. In this review, we will introduce diverse molecular signaling pathways that are aberrantly activated in HCC, focusing on YAP/TAZ, Hedgehog, and Wnt/β-catenin signaling pathways, and discuss potential therapeutic strategies targeting the signaling pathways in HCC.

Indexed as

animal modelsHedgehoghepatocellular carcinomatarget therapyWnt/β-cateninYAP/TAZ

Identifiers

PMID35453784
PMCPMC9027240
OpenAlexW4223435091

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.