Evidence map›Paper›PMID 29532226›Full record

ArticleMolecular and cellular biochemistry2018

A novel matrine derivative WM622 inhibits hepatocellular carcinoma by inhibiting PI3K/AKT signaling pathways.

Xiao Sun, Xiao-Bin Zhuo, Yi-Ping Hu, Xuan Zheng, Qing-Jie Zhao

Abstract read
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In one paragraph

Article in Molecular and cellular biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  9. SALL4 Oncogenic Function in Cancers: Mechanisms and Therapeutic Relevance.International journal of molecular sciences · 2022
    Review
  10. Article
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  15. Anti-Tumor Activities of Bioactive Phytochemicals inCancer management and research · 2020
    Review
  16. [Matrine suppresses stemness of hepatocellular carcinoma cells by regulating β-catenin signaling pathway].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2019
    Article
  17. 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

5 authors at 2 institutions in 1 country.

Xiao SunDepartment of Cell Biology, Second Military Medical University, Shanghai, 200433, People's Republic of China.
Xiao-Bin ZhuoDepartment of Organic Chemistry, Second Military Medical University, Shanghai, 200433, People's Republic of China.
Yi-Ping HuDepartment of Cell Biology, Second Military Medical University, Shanghai, 200433, People's Republic of China.
Xuan ZhengClinical Nutrition Department, Changhai Hospital, Second Military Medical University, Shanghai, 200433, People's Republic of China. zhengxuandc@126.com.
Qing-Jie ZhaoDepartment of Organic Chemistry, Second Military Medical University, Shanghai, 200433, People's Republic of China. qjzhao@smmu.edu.cn.
Second Military Medical University · CNChanghai Hospital · CN

Funding

National Natural Science Foundation of China 21502225National Natural Science Foundation of China 30872120/H2603The Shanghai Pujiang Talent program 17PJD042
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is among the most common lethal cancers of the digestive system with poor prognosis rates and ineffective therapeutic options. Matrine, a traditional Chinese medicine found in the roots of sophora species, has been used in the clinical treatment of liver fibrosis, chronic hepatitis B and other diseases. We have synthesized a matrine derivatives named WM622 (C26H35ON3S2) with a significant inhibitory effect on transplanted tumors in vivo. The half inhibitory concentration (IC50) of WM622 is 34 µM, which is much lower than matrine. WM622 inhibited the proliferation and promoted apoptosis of hepatocellular carcinoma cells significantly, and the cell cycle was blocked in G0/G1 phase. The protein phosphorylation levels of EGFR, AKT, PI3K and GSK3β (p-EGFR, p-AKT, p-PI3K, and p-GSK3β) were also decreased by WM622 treatment dose dependently. In tumor-bearing mice, WM622 could reduce the tumor volumes. In conclusion, the study demonstrated that WM622 could inhibit the proliferation of the hepatocellular carcinoma both in vivo and in vitro by inducing apoptosis, blocking cell cycle in G0/G1 phase and inhibiting the PI3K/AKT signal pathways.

Indexed as

AlkaloidsQuinolizinesAnimalsCarcinoma, HepatocellularCell Line, TumorG1 Phase Cell Cycle CheckpointsHumansLiver NeoplasmsMaleMatrinesMiceMice, Inbred BALB CMice, NudePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktResting Phase, Cell CycleAlkaloidsMatrinesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktQuinolizinesAKTHepatocellular carcinomaMatrine derivativePI3K

Identifiers

PMID29532226
OpenAlexW2791240642

What OpenQuestion holds

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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.