Evidence map›Paper›PMID 29208003›Full record

ArticleJournal of experimental & clinical cancer research : CR2017

FOXA1 inhibits hepatocellular carcinoma progression by suppressing PIK3R1 expression in male patients.

Shujiao He, Junyi Zhang, Wan Zhang, Fengsheng Chen, Rongcheng Luo

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

31 citing papers in PubMed, 49 citations in OpenAlex.

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  20. Investigation of Anti-Liver Cancer Activity of the Herbal Drug FDY003 Using Network Pharmacology.Evidence-based complementary and alternative medicine : eCAM · 2022
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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 2 institutions in 1 country.

Shujiao HeCancer Center, Southern Medical University, Guangzhou, Guangdong, 510315, China.
Junyi ZhangCancer Center, Southern Medical University, Guangzhou, Guangdong, 510315, China.
Wan ZhangCancer Center, Southern Medical University, Guangzhou, Guangdong, 510315, China.
Fengsheng ChenCancer Center, Southern Medical University, Guangzhou, Guangdong, 510315, China. fsc0126@163.com.
Rongcheng LuoCancer Center, Southern Medical University, Guangzhou, Guangdong, 510315, China. luorc02@vip.163.com.
Southern Medical University · CNTCM-Intigrated Cancer Center of Southern Medical University · CN

Funding

National Natural Science Foundation of China 81502378Natural Science Foundation of Guangdong Province 2016A030313533Research Foundation for the Returned Overseas Chinese Scholars of Southern Medical University LX2016N008Science and Technology Foundation of Guangzhou 201604020009Technology Planning Project of Guangdong Province 2016ZC0056
6 · The paper itself

Abstract

backgroundForkhead box A1 (FOXA1) expression is associated with various types of tumors; however, the function and underlying mechanism of FOXA1 in the development of hepatocellular carcinoma (HCC) remains obscure.

methodsHere, we investigated the role of FOXA1 in the development of HCC by applying gene function gain and loss analysis to HepG2 and Hep3B cell lines, and comparing outcomes with those of clinical HCC samples.

resultsPhosphoinositide-3-kinase regulatory subunit 1 (PIK3R1), which encodes protein PI3Kp85 (p85), was identified as a FOXA1 target gene. Analyses of the mechanism and function revealed that FOXA1 suppresses hepatocellular carcinoma cell viability and motility by inhibiting PI3K/Akt signaling through direct inhibition of PIK3R1 transcription. Moreover, in clinical samples from male HCC patients, FOXA1 expression was much lower, whereas PI3Kp85 levels were much higher in tumor than in non-tumor tissues. Elevated PI3Kp85 is an unfavorable factor in HCC.

conclusionsAs a tumor suppressor, FOXA1 targets PIK3R1 directly to inhibit PI3K/Akt signaling pathway, thus exerting a negative regulatory effect on proliferation, migration, and invasion of HCC in male patients.

Indexed as

Phosphoinositide-3 Kinase InhibitorsCarcinoma, HepatocellularCell Line, TumorClass Ia Phosphatidylinositol 3-KinaseDisease ProgressionHepatocyte Nuclear Factor 3-alphaHep G2 CellsHumansLiver NeoplasmsMalePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionTransfectionClass Ia Phosphatidylinositol 3-KinaseFOXA1 protein, humanHepatocyte Nuclear Factor 3-alphaPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsPIK3R1 protein, humanProto-Oncogene Proteins c-aktFOXA1Hepatocellular carcinomaPI3K/AktPIK3R1/PI3Kp85

Identifiers

PMID29208003
PMCPMC5718070
OpenAlexW2775414517

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.