Evidence map›Paper›PMID 29731901›Full record

ArticleOncology letters2018

Tetrandrine suppresses adhesion, migration and invasion of human colon cancer SW620 cells via inhibition of nuclear factor-κB, matrix metalloproteinase-2 and matrix metalloproteinase-9 signaling pathways.

Ta-Kuo Juan, Kuo-Ching Liu, Chao-Lin Kuo, Mei-Due Yang, Yung-Lin Chu, Jiun-Long Yang, Ping-Ping Wu, Yi-Ping Huang, Kuang-Chi Lai, Jing-Gung Chung

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 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
2.5field-weighted citation impact, top 11% 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, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Tetrandrine Suppresses Human Brain Glioblastoma GBM 8401/Molecules (Basel, Switzerland) · 2021
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

10 authors at 1 institution in 1 country.

Ta-Kuo JuanDepartment of Biological Science and Technology, China Medical University, Taichung 404, Taiwan, R.O.C.
Kuo-Ching LiuDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 404, Taiwan, R.O.C.
Chao-Lin KuoChinese Medicine Resources, China Medical University, Taichung 404, Taiwan, R.O.C.
Mei-Due YangDepartment of Surgery, China Medical University Hospital, Taichung 404, Taiwan, R.O.C.
Yung-Lin ChuInternational Master's Degree Program in Food Science, International College, National Pingtung University of Science and Technology, Pingtung 912, Taiwan, R.O.C.
Jiun-Long YangDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 404, Taiwan, R.O.C.
Ping-Ping WuSchool of Pharmacy, China Medical University, Taichung 404, Taiwan, R.O.C.
Yi-Ping HuangDepartment of Physiology, China Medical University, Taichung 404, Taiwan, R.O.C.
Kuang-Chi LaiSchool of Medicine, China Medical University, Taichung 404, Taiwan, R.O.C.
Jing-Gung ChungDepartment of Biological Science and Technology, China Medical University, Taichung 404, Taiwan, R.O.C.
China Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tetrandrine (TET) exhibits biological activities, including anticancer activity. In Chinese medicine, TET has been used to treat hypertensive and arrhythmic conditions and has been demonstrated to induce cytotoxic effects on human cancer cell lines. However, to the best of the author's knowledge, no previous studies have revealed that TET affects cell metastasis in SW620 human colon cancer cells. The present study demonstrated that TET decreased the cell number and inhibited cell adhesion and mobility of SW620 cells. Furthermore, a wound healing assay was performed to demonstrate that TET suppressed cell movement, and Transwell chamber assays were used to reveal that TET suppressed the cell migration and invasion of SW620 cells. Western blotting demonstrated that TET significantly reduced protein expression levels of SOS Ras/Rac guanine nucleotide exchange factor 1, phosphatidylinositol 3-kinase, growth factor receptor bound protein 2, phosphorylated (p)-c Jun N-terminal kinase 1/2, p-p38, p38, 14-3-3, Rho A, β-catenin, nuclear factor-κB p65, signal transducer and activator of transcription-1 and cyclooxygenase-2, in comparison with untreated SW620 cells. Overall, the results of the present study suggested that TET may be used as a novel anti-metastasis agent for the treatment of human colon cancer in the future.

Indexed as

invasionmatrix metalloproteinase-2matrix metalloproteinase-9migrationnuclear factor-κB p65SW620 human colon cancer cellstetrandrine

Identifiers

PMID29731901
PMCPMC5921181
OpenAlexW2791722377

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.