Evidence map›Paper›PMID 30589500›Full record

ArticleJournal of cellular and molecular medicine2018

HMQ-T-B10 induces human liver cell apoptosis by competitively targeting EphrinB2 and regulating its pathway.

Bingling Dai, Xianpeng Shi, Nan Ma, Weina Ma, Yanmin Zhang, Tianfeng Yang, Jie Zhang, Langchong He

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  7. Review
  8. Anthracycline chemicals with anthracyclinone structure exert antitumor effects by inhibiting angiogenesis and lymphangiogenesis in a xenografted gastric tumor model.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2023
    Article
  9. Review
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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 1 institution in 1 country.

Bingling DaiSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, China.ORCID 0000-0002-5625-2579
Xianpeng ShiSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, China.
Nan MaSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, China.
Weina MaSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, China.
Yanmin ZhangSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, China.
Tianfeng YangSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, China.
Jie ZhangSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, China.
Langchong HeSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, China.
Xi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a highly prevalent cancer worldwide and it is necessary to discover and develop novel preventive strategies and therapeutic approaches for HCC. Herein, we report that EphrinB2 expression is correlated with liver cancer progression. Moreover, by using phosphorylated proteomics array, we reveal a pro-apoptosis protein whose phosphorylation and activation levels are up-regulated upon EphrinB2 knockdown. These results suggest that EphrinB2 may act as an anti-apoptotic protein in liver cancer cells. We also explored the therapeutic potential of HMQ-T-B10 (B10), which was designed and synthesized in our laboratory, for HCC and its underlying mechanisms in vitro and in vivo. Our data demonstrate that B10 could bind EphrinB2 and show inhibitory activity on human liver cancer cells. Moreover, induction of human liver cancer cell apoptosis by B10 could be augmented upon EphrinB2 knockdown. B10 inhibited HCC cell growth and induced HCC cell apoptosis by repressing the EphrinB2 and VEGFR2 signalling pathway. Growth of xenograft tumours derived from Hep3B in nude mice was also significantly inhibited by B10. Collectively, these findings highlight the potential molecular mechanisms of B10 and its potential as an effective antitumour agent for HCC.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCarcinoma, HepatocellularCell ProliferationEphrin-B2Gene Expression Regulation, NeoplasticHep G2 CellsHumansLiverLiver NeoplasmsMicePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionVascular Endothelial Growth Factor Receptor-2Antineoplastic AgentsEFNB2 protein, humanEphrin-B2KDR protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktVascular Endothelial Growth Factor Receptor-2apoptosisEphrinB2HMQ‐T‐B10liver cancer cell

Identifiers

PMID30589500
PMCPMC6201340
OpenAlexW2892095304

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.