Evidence map›Paper›PMID 36557813›Full record

ArticleMolecules (Basel, Switzerland)2022

AHNAK Contributes to Hepatocellular Carcinoma Growth by Interacting with IGF-1R.

Kang Li, Ke Song, Yuli Hou, Yuan Tian, Huijuan Wang, Libo Sun, Ang Li, Yonghong Zhang

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

7 citing papers in PubMed, 7 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

8 authors at 2 institutions in 1 country.

Kang LiBiomedical Information Center, Beijing You'An Hospital, Capital Medical University, Beijing 100069, China.
Ke SongDepartment of Histology and Embryology, School of Basic Medical Sciences, Capital Medical University, Beijing 100069, China.
Yuli HouDepartment of Clinical Laboratory, Xuanwu Hospital, National Clinical Research Center for Geriatric Diseases, Capital Medical University, Beijing 100053, China.
Yuan TianBeijing Institute of Hepatology, Beijing You'An Hospital, Capital Medical University, Beijing 100069, China.
Huijuan WangBeijing Institute of Hepatology, Beijing You'An Hospital, Capital Medical University, Beijing 100069, China.
Libo SunDepartment of Hepatobiliary Surgery, Beijing You'An Hospital, Capital Medical University, Beijing 100069, China.
Ang LiBiomedical Information Center, Beijing You'An Hospital, Capital Medical University, Beijing 100069, China.
Yonghong ZhangBiomedical Information Center, Beijing You'An Hospital, Capital Medical University, Beijing 100069, China.
Beijing YouAn Hospital · CNCapital Medical University · CN

Funding

Beijing Key Laboratory BZ0373Beijing Municipal Science & Technology Commission Z171100001017078Beijing You'An Hospital BJYAHKF2021003,YNKTQN2021007Capital's Funds of Health Improvement and Research CFH2020-1-2182National Key Research and Development Project 2020YFE0202400Sail Plan" from Beijing Hospital Authority XMLX201711
6 · The paper itself

Abstract

Neuroblast differentiation-associated protein AHNAK, a large structural scaffold protein, remains mysterious in biological processes. AHNAK plays a suppressive or progressive role in different types of cancers. To investigate the role of the AHNAK in hepatocellular carcinoma (HCC), cell viability assays were performed to determine the cell proliferation of the stable AHNAK-knockdown HepG2 cell line; co-immunoprecipitation (Co-IP) and liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) were performed on HCC and matched paracancerous (MPC) tissues. The Metascape platform was used for enrichment analyses; the "ComplexHeatmap" package was applied for cluster analyses and visualization. Co-IP, Western botting and immunofluorescence double staining were performed to assess the interactions between AHNAK and insulin-like growth factor 1 receptor (IGF-1R). AHNAK silencing reduced the viability of HepG2 cells; the interactome in HCC and MPC tissues enriched 204 pathways and processes, which partially reflected the signature of HCC field cancerization. AHNAK could co-localize and interact with IGF-1R. These results suggested that the AHNAK complex contributes to HCC growth, potentially by interacting with IGF-1R.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsCell Line, TumorCell ProliferationChromatography, LiquidHumansMembrane ProteinsNeoplasm ProteinsSignal TransductionTandem Mass SpectrometryAHNAK protein, humanMembrane ProteinsNeoplasm Proteinsfield cancerizationhepatocellular carcinoma (HCC)insulin-like growth factor 1 receptor (IGF-1R)interactomeneuroblast differentiation-associated protein AHNAK

Identifiers

PMID36557813
PMCPMC9782793
OpenAlexW4311859198

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.