Evidence map›Paper›PMID 28492540›Full record

ArticleCell death & disease2017

NMI inhibits cancer stem cell traits by downregulating hTERT in breast cancer.

Xu Feng, Xiangdong Xu, Xiangsheng Xiao, Kun Zou, Wendan Yu, Jiali Wu, Ranran Tang, Yue Gao, Jiaojiao Hao, Xinrui Zhao and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

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  14. Expression of LGR5 in oral squamous cell carcinoma and its correlation to vasculogenic mimicry.International journal of clinical and experimental pathology · 2017
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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

16 authors at 5 institutions in 1 country.

Xu FengInstitute of Cancer Stem Cell & The First Affiliated Hospital, Dalian Medical University, Dalian, China.
Xiangdong XuDepartment of Thyroid & Breast Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xiangsheng XiaoSun Yat-sen University Cancer Center, State Key Laboratory of Oncology, Collaborative Innovation Center of Cancer Medicine, Guangzhou, China.
Kun ZouInstitute of Cancer Stem Cell & The First Affiliated Hospital, Dalian Medical University, Dalian, China.
Wendan YuInstitute of Cancer Stem Cell & The First Affiliated Hospital, Dalian Medical University, Dalian, China.
Jiali WuSun Yat-sen University Cancer Center, State Key Laboratory of Oncology, Collaborative Innovation Center of Cancer Medicine, Guangzhou, China.
Ranran TangInstitute of Cancer Stem Cell & The First Affiliated Hospital, Dalian Medical University, Dalian, China.
Yue GaoInstitute of Cancer Stem Cell & The First Affiliated Hospital, Dalian Medical University, Dalian, China.
Jiaojiao HaoInstitute of Cancer Stem Cell & The First Affiliated Hospital, Dalian Medical University, Dalian, China.
Xinrui ZhaoInstitute of Cancer Stem Cell & The First Affiliated Hospital, Dalian Medical University, Dalian, China.
Yina LiaoInstitute of Cancer Stem Cell & The First Affiliated Hospital, Dalian Medical University, Dalian, China.
Yiming ChenInstitute of Cancer Stem Cell & The First Affiliated Hospital, Dalian Medical University, Dalian, China.
Wenlin HuangSun Yat-sen University Cancer Center, State Key Laboratory of Oncology, Collaborative Innovation Center of Cancer Medicine, Guangzhou, China.
Wei GuoInstitute of Cancer Stem Cell & The First Affiliated Hospital, Dalian Medical University, Dalian, China.
Lan KangInstitute of Cancer Stem Cell & The First Affiliated Hospital, Dalian Medical University, Dalian, China.
Wuguo DengSun Yat-sen University Cancer Center, State Key Laboratory of Oncology, Collaborative Innovation Center of Cancer Medicine, Guangzhou, China.
Dalian Medical University · CNFirst Affiliated Hospital of Dalian Medical University · CNSun Yat-sen University Cancer Center · CNSun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

N-myc and STAT interactor (NMI) has been proved to bind to different transcription factors to regulate a variety of signaling mechanisms including DNA damage, cell cycle and epithelial-mesenchymal transition. However, the role of NMI in the regulation of cancer stem cells (CSCs) remains poorly understood. In this study, we investigated the regulation of NMI on CSCs traits in breast cancer and uncovered the underlying molecular mechanisms. We found that NMI was lowly expressed in breast cancer stem cells (BCSCs)-enriched populations. Knockdown of NMI promoted CSCs traits while its overexpression inhibited CSCs traits, including the expression of CSC-related markers, the number of CD44

Indexed as

Down-RegulationGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticBreast NeoplasmsFemaleHumansIntracellular Signaling Peptides and ProteinsMCF-7 CellsNeoplastic Stem CellsTelomeraseIntracellular Signaling Peptides and ProteinsNMI protein, humanTelomeraseTERT protein, human

Identifiers

PMID28492540
PMCPMC5520720
OpenAlexW2613056879

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.