Evidence map›Paper›PMID 31007696›Full record

ArticleJournal of research in medical sciences : the official journal of Isfahan University of Medical Sciences2019

Inhibition of hepatocellular carcinoma cell proliferation, migration, and invasion by a disintegrin and metalloproteinase-17 inhibitor TNF484.

Changhong Xia, Dongsheng Zhang, Yanmei Li, Jie Chen, Haibo Zhou, Long Nie, Yanyan Sun, Siyan Guo, Jianbiao Cao, Fangzheng Zhou and 1 more

Abstract read
In one paragraph

Article in Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

11 authors.

Changhong XiaDepartment of Ultrasound, Chinese People's Liberation Army General Hospital, Beijing, China.
Dongsheng ZhangDepartment of Oncology, Suizhou Hospital, Hubei University of Medicine, Suizhou, China.
Yanmei LiDepartment of Oncology, Suizhou Hospital, Hubei University of Medicine, Suizhou, China.
Jie ChenDepartment of Oncology, Suizhou Hospital, Hubei University of Medicine, Suizhou, China.
Haibo ZhouDepartment of Oncology, Suizhou Hospital, Hubei University of Medicine, Suizhou, China.
Long NieDepartment of Oncology, Suizhou Hospital, Hubei University of Medicine, Suizhou, China.
Yanyan SunDepartment of Oncology, Suizhou Hospital, Hubei University of Medicine, Suizhou, China.
Siyan GuoDepartment of Oncology, Suizhou Hospital, Hubei University of Medicine, Suizhou, China.
Jianbiao CaoDepartment of Liver Disease, Army General Hospital of PLA, Beijing, China.
Fangzheng ZhouDepartment of Oncology, Suizhou Hospital, Hubei University of Medicine, Suizhou, China.
Junlai LiDepartment of Ultrasound, Chinese People's Liberation Army General Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of this study was to test the effect of TNF484 on cell proliferation, migration, and invasion of hepatocellular carcinoma (HCC) cells. MATERIALS AND

methodsVarious doses (0, 1, 10, 50, and 100 nM) of TNF484 were applied to the HepG2 and Bel7402 cells, and cell proliferation was measured by using 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyl tetrazolium bromide assay after 72 h. Cell migration rate was measured using the xCELLigence system, and the cell invasion ability was examined by the three-dimensional spheroid BME cell invasion assay. The expression level of ADAM17 was also measured with RT-PCR.

resultsWith the treatment of TNF484, the cell proliferation of HepG2 and Bel7402 cells was inhibited in a dose-dependent manner. Moreover, under TNF484 treatment, the cell migration rate as well as cell invasion ability of the HepG2 and Bel7402 cells were suppressed.

conclusionTNF484 could inhibit the cell proliferation, migration, and invasion of some HCC cell lines, making it a potential therapeutic option for liver cancer treatment.

Indexed as

ADAM17hepatocellular carcinomaTNF484

Identifiers

PMID31007696
PMCPMC6450222

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.