Evidence map›Paper›PMID 31915594›Full record

ArticleAnalytical cellular pathology (Amsterdam)2019

The Effect of Protein FAM172A on Proliferation in HepG2 Cells and Investigation of the Possible Molecular Mechanism.

Hong Zhao, Yujie Wang, Yufeng Liu, Xiaohua Hao, Hongshan Wei, Wen Xie

Open access · goldAbstract read
In one paragraph

Article in Analytical cellular pathology (Amsterdam), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 51% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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 2 institutions in 1 country.

Hong ZhaoLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Yujie WangDepartment of Infectious Diseases, Peking University International Hospital, Beijing 102206, China.ORCID https://orcid.org/0000-0001-5785-0581
Yufeng LiuLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Xiaohua HaoInstitute of Infectious Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Hongshan WeiInstitute of Infectious Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.ORCID https://orcid.org/0000-0001-8893-653X
Wen XieLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.ORCID https://orcid.org/0000-0002-7314-8175
Capital Medical University · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn our previous study, we found that the FAM172A recombinant protein could promote proliferation of L02 cells. However, the underlying mechanisms are still unknown. The present study was aimed at investigating the effect of FAM172A on proliferation of HepG2 cells and exploring the possible molecular mechanisms and its role in hepatocellular carcinoma (HCC).

methodsCell proliferation was measured by MTT assay. Western blot test was carried out to investigate the mechanism. Rabbit antibodies against FAM172A and membrane proteins isolated from lysate of HepG2 cell were coprecipitated and the resultant precipitates were analyzed by mass spectrum.

resultsThe MTT assay showed that recombinant protein FAM172A isoform 1 (FAM172A-1) could induce HepG2 cell proliferation at the concentration of 10-100 ng/mL, while protein FAM172A isoform 3 (FAM172A-3) was at the concentration of 80-100 ng/mL. Western blot demonstrated that both FAM172A-1 and FAM172A-3 could activate the mitogen-activated protein kinase/extracellular signal-regulated protein kinase (MAPK/ERK) pathway and the phosphatidylinositol 3-kinase/threonine-protein kinase (PI3K/Akt) pathway. Mass spectrum analysis suggested that there were some membrane proteins interacting with FAM172A. Several candidate interacting proteins might mediate proliferation signals induced by FAM172A recombinant protein, including seven membrane proteins.

conclusionIn conclusion, FAM172A recombinant protein could induce proliferation of HepG2 cells, in which the MAPK/ERK and PI3K/Akt signaling pathways might be involved. The role of FAM172A in HepG2 cell proliferation also indicated its possible involvement in HCC. The receptor of FAM172A on cells still needs to be exploited.

Indexed as

Carcinoma, HepatocellularCell ProliferationExtracellular Signal-Regulated MAP KinasesHep G2 CellsHumansLiver NeoplasmsMass SpectrometryMembrane ProteinsPhosphatidylinositol 3-KinasesProtein IsoformsProteinsRecombinant ProteinsSignal TransductionARB2A protein, humanExtracellular Signal-Regulated MAP KinasesMembrane ProteinsPhosphatidylinositol 3-KinasesProtein IsoformsProteinsRecombinant Proteins

Identifiers

PMID31915594
PMCPMC6930761
OpenAlexW2994823552

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LicenceCC BY
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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.