Evidence map›Paper›PMID 30141114›Full record

ArticlePathology oncology research : POR2019

Non-Coding RNA Pvt1 Promotes Cancer Stem Cell-Like Traits in Nasopharyngeal Cancer via Inhibiting miR-1207.

Meng Cui, Yu Chang, Qi-Gen Fang, Wei Du, Jun-Fu Wu, Ji-Heng Wang, Shan-Ting Liu, Su-Xia Luo

Abstract read
PubMed Publisher
In one paragraph

Article in Pathology oncology research : POR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

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  7. lncRNA PVT1: a novel oncogene in multiple cancers.Cellular & molecular biology letters · 2022
    Review
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  13. Cancer stem cells: a major culprit of intra-tumor heterogeneity.American journal of cancer research · 2021
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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

8 authors at 2 institutions in 1 country.

Meng CuiDepartment of Head & Neck and Thyroid, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, 450008, People's Republic of China.
Yu ChangDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450008, People's Republic of China.
Qi-Gen FangDepartment of Head & Neck and Thyroid, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, 450008, People's Republic of China.
Wei DuDepartment of Head & Neck and Thyroid, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, 450008, People's Republic of China.
Jun-Fu WuDepartment of Head & Neck and Thyroid, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, 450008, People's Republic of China.
Ji-Heng WangDepartment of Head & Neck and Thyroid, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, 450008, People's Republic of China.
Shan-Ting LiuDepartment of Head & Neck and Thyroid, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, 450008, People's Republic of China.
Su-Xia LuoDepartment of Medical Oncology, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, 450008, People's Republic of China. luosuxia8275@sina.com.
Zhengzhou University · CNFirst Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nasopharyngeal carcinoma (NPC) is a kind of head-neck malignant tumor. lncRNA-PVT1 can promote the proliferation of carcinoma cells, and induce cells to have stem cell-like potentials. However, the function of PVT1 in NPC cells is not clear. The expressions of lncRNA-PVT1 and the expressions of the stem cell markers in NPC tissues or cell lines were investigated by qRT-PCR or western blot. The cell proliferation, and the ability of NPC cells to form spherical, clonal colonies were investigated by MTT assay, colony formation assay, and tumor-sphere formation assay. Cancer stem cells surface markers were detected by flow cytometry and western blot. PI3K/AKT signal activation in NPC cells was determined by western blot. PVT1 was significantly up-regulated in both NPC tissues and cell lines and associated with poor prognosis. PVT1 knockdown reduced NPC cells viability, clonogenicity, the cell surface CD44+/CD24- stem phenotype, and the expressions of the stem cell markers in NPC cells, including Oct4, c-Myc, SOX2, and ALDH. Furthermore, PVT1 negatively regulates the expression levels of miR-1207 in NPC cells and spheres cells, which is critical for NPC stemness. Knockdown of miR-1207 promoted stem phenotype and the expressions of the stem cell markers in NPC cells. Moreover, phosphor-PI3K (p-PI3K) and phosphor-AKT (p-AKT) were found to be down-regulated after PVT1 siRNAs transfection in NPC cells. And miR-1207 inhibitor transfection reversed the all the effects brought by PVT1 knockdown. Pvt1 promotes cancer stem cell-like properties in NPC cells via inhibiting miR-1207 and activating the PI3K/AKT signal pathway.

Indexed as

Gene Expression Regulation, NeoplasticApoptosisBiomarkers, TumorCell ProliferationHumansMicroRNAsNasopharyngeal NeoplasmsNeoplastic Stem CellsPhenotypePrognosisRNA, Long NoncodingSurvival RateTumor Cells, CulturedBiomarkers, TumorMicroRNAsMIRN1207 microRNA, humanPVT1 long-non-coding RNA, humanRNA, Long NoncodingmiR-1207Nasopharyngeal carcinomaPI3K/AKTPVT1Tumor stem cell

Identifiers

PMID30141114
OpenAlexW2888415345

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.