Evidence map›Paper›PMID 26830149›Full record

ArticleScientific reports2016

Nifuroxazide exerts potent anti-tumor and anti-metastasis activity in melanoma.

Yongxia Zhu, Tinghong Ye, Xi Yu, Qian Lei, Fangfang Yang, Yong Xia, Xuejiao Song, Li Liu, Hongxia Deng, Tiantao Gao and 9 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 71 citations in OpenAlex.

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  17. Frontiers in cell and developmental biology · 2019
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 3 institutions in 2 countries.

Yongxia ZhuState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Tinghong YeState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Xi YuCollege of agricultural and life sciences, University of Wisconsin-Madison, Madison, WI53706, USA.
Qian LeiState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Fangfang YangState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Yong XiaState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Xuejiao SongState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Li LiuState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Hongxia DengState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Tiantao GaoState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Cuiting PengState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Weiqiong ZuoState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Ying XiongDepartment of Pharmacy, Xinqiao Hospital, Third Military Medical University, Chongqing, 404100, China.
Lidan ZhangState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Ningyu WangState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Lifeng ZhaoState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Yongmei XieState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Luoting YuState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Yuquan WeiState Key Laboratory of Biotherapy/ Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, Sichuan, China.
Sichuan University · CNArmy Medical University · CNUniversity of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanoma is a highly malignant neoplasm of melanocytes with considerable metastatic potential and drug resistance, explaining the need for new candidates that inhibit tumor growth and metastasis. The signal transducer and activator of the transcription 3 (Stat3) signaling pathway plays an important role in melanoma and has been validated as promising anticancer target for melanoma therapy. In this study, nifuroxazide, an antidiarrheal agent identified as an inhibitor of Stat3, was evaluated for its anti-melanoma activity in vitro and in vivo. It had potent anti-proliferative activity against various melanoma cell lines and could induce G2/M phase arrest and cell apoptosis. Moreover, nifuroxazide markedly impaired melanoma cell migration and invasion by down-regulating phosphorylated-Src, phosphorylated-FAK, and expression of matrix metalloproteinase (MMP) -2, MMP-9 and vimentin. It also significantly inhibited tumor growth without obvious side effects in the A375-bearing mice model by inducing apoptosis and reducing cell proliferation and metastasis. Notably, nifuroxazide significantly inhibited pulmonary metastases, which might be associated with the decrease of myeloid-derived suppressor cells (MDSCs). These findings suggested that nifuroxazide might be a potential agent for inhibiting the growth and metastasis of melanoma.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell Line, TumorCell MovementCell ProliferationCell SurvivalDisease Models, AnimalG2 Phase Cell Cycle CheckpointsHumansHydroxybenzoatesMelanomaMelanoma, ExperimentalMitochondriaNeoplasm MetastasisNitrofuransAntineoplastic AgentsHydroxybenzoatesnifuroxazideNitrofurans

Identifiers

PMID26830149
PMCPMC4735744
OpenAlexW2413114447

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.