Evidence map›Paper›PMID 31823303›Full record

ArticleJournal of physiology and biochemistry2020

Arginine deprivation inhibits pancreatic cancer cell migration, invasion and EMT via the down regulation of Snail, Slug, Twist, and MMP1/9.

Huan Wang, Qing-Fang Li, H Y Chow, S C Choi, Yun-Chung Leung

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of physiology and biochemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 52 citations in OpenAlex.

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  14. Discovery and Targeting of a Noncanonical Mechanism of Sarcoma Resistance to ADI-PEG20 Mediated by the Microenvironment.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
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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 2 countries.

Huan WangDepartment of Cancer Center, General Hospital of PLA, Beijing, 100853, People's Republic of China.
Qing-Fang LiDepartment of Cancer Center, General Hospital of PLA, Beijing, 100853, People's Republic of China.
H Y ChowDepartment of Applied Biology and Chemical Technology and Lo Ka Chung Centre for Natural Anti-Cancer Drug Development, Hong Kong Polytechnic University, 11 Yuk Choi Road, Hung Hom, Kowloon, Hong Kong, China.
S C ChoiDepartment of Applied Biology and Chemical Technology and Lo Ka Chung Centre for Natural Anti-Cancer Drug Development, Hong Kong Polytechnic University, 11 Yuk Choi Road, Hung Hom, Kowloon, Hong Kong, China.
Yun-Chung LeungDepartment of Applied Biology and Chemical Technology and Lo Ka Chung Centre for Natural Anti-Cancer Drug Development, Hong Kong Polytechnic University, 11 Yuk Choi Road, Hung Hom, Kowloon, Hong Kong, China. bctleung@polyu.edu.hk.ORCID http://orcid.org/0000-0001-7753-6522
Hong Kong Polytechnic University · HKChinese PLA General Hospital · CN

Funding

Beijing Nova Program Z171100001117112Hong Kong Scholars Program G-YZ14Lo Ka Chung Charity fund 1-BB62Niche Areas Fund 1-BB63Translational Medicine Program of Chinese PLA General Hospital 2017TM-022Youth Talents Promotion Project 17-JCJQ-QT-030
6 · The paper itself

Abstract

Arginine deprivation is currently being evaluated for its efficacy and safety in clinical trials aimed at combating tumors. However, the cellular signaling and molecular changes in response to such deprivation have not been systematically deciphered. Here, we evaluate the effect of arginine deprivation on human pancreatic cancer cells, with respect to their migratory and invasive potentials and their ability to undergo epithelial-mesenchymal transition (EMT). The transcription factors Snail, Slug, and Twist are regulators of EMT, as indicated by the suppression of E-cadherin and other epithelial markers and adhesion molecules. Our data indicated that arginine starvation inhibited the migration and impaired the adhesion and invasion of the pancreatic cancer cells, decreased Snail, Slug, and Twist expression, and increased E-cadherin expression without altering the expression of vimentin. It is well known that matrix metalloproteinases (MMPs) are important for the events that underlie tumor dissemination. Arginine starvation inhibited the expression of MMP-1 and MMP-9. Furthermore, the PI3K/Akt pathway was altered when the pancreatic cancer cells underwent arginine deprivation as exhibited by the decreased Akt phosphorylation. Thus, these data reveal that arginine deprivation has the potential to decrease the metastatic ability of pancreatic cancer cells.

Indexed as

Cell MovementEpithelial-Mesenchymal TransitionAnimalsAntigens, CDArginineCadherinsCarcinoma, Pancreatic DuctalCell Line, TumorDown-RegulationHumansMatrix Metalloproteinase 1Matrix Metalloproteinase 9MiceMice, SCIDNeoplasm InvasivenessNuclear ProteinsAntigens, CDArginineCadherinsCDH1 protein, humanMatrix Metalloproteinase 1Matrix Metalloproteinase 9MMP1 protein, humanMMP9 protein, humanNuclear ProteinsProto-Oncogene Proteins c-aktSNAI1 protein, humanSnail Family Transcription FactorsTWIST1 protein, humanTwist-Related Protein 1Arginine deprivationEMTinvasionmigrationpancreatic cancer cells

Identifiers

PMID31823303
OpenAlexW2994928211

What OpenQuestion holds

Textmetadata
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.