Evidence map›Paper›PMID 28168162›Full record

ArticleAnalytical cellular pathology (Amsterdam)2017

Long Noncoding RNA MIR4697HG Promotes Cell Growth and Metastasis in Human Ovarian Cancer.

Li-Qian Zhang, Su-Qing Yang, Ying Wang, Qiao Fang, Xian-Jun Chen, Hong-Sheng Lu, Ling-Ping Zhao

Open access · goldAbstract read
In one paragraph

Article in Analytical cellular pathology (Amsterdam), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. [Knockdown of long non-coding RNABeijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2022
    Article
  3. Article
  4. Review
  5. Article
  6. ERK/MAPK signalling pathway and tumorigenesis.Experimental and therapeutic medicine · 2020
    Review
  7. Long intergenic noncoding RNA LINC00284 knockdown reduces angiogenesis in ovarian cancer cellsFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. 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

7 authors at 1 institution in 1 country.

Li-Qian ZhangGynecology Department, Taizhou Central Hospital, Zhejiang 318000, China.
Su-Qing YangGynecology Department, Taizhou Central Hospital, Zhejiang 318000, China.
Ying WangGynecology Department, Taizhou Central Hospital, Zhejiang 318000, China.
Qiao FangGynecology Department, Taizhou Central Hospital, Zhejiang 318000, China.
Xian-Jun ChenClinical Laboratory, Taizhou Central Hospital, Zhejiang 318000, China.
Hong-Sheng LuPathology Department, Taizhou Central Hospital, Zhejiang 318000, China.
Ling-Ping ZhaoGynecology Department, Taizhou Central Hospital, Zhejiang 318000, China.ORCID 0000-0002-0573-8026
Taizhou Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer is one of the three most common gynecological malignant tumors worldwide. The prognosis of patients suffering from this malignancy remains poor because of limited therapeutic strategies. Herein, we investigated the role of a long noncoding RNA named MIR4697 host gene (MIR4697HG) in the cell growth and metastasis of ovarian cancer. Results showed that the transcriptional level of MIR4697HG in cancerous tissues increased twofold compared with that in adjacent noncancerous tissues. MIR4697HG was differentially expressed in ovarian cancer cell lines, with the highest levels in OVCAR3 and SKOV3 cells. MIR4697HG knockdown by specific shRNA significantly inhibited cell proliferation and colony formation in both OVCAR3 and SKOC3 cells. Consistently, in a xenograft model of ovarian cancer, MIR4697HG depletion also significantly restricted tumor volumes and weights. Furthermore, MIR4697HG knockdown inhibited cell migration and invasion capacities. Invasion ability was inhibited by 58% in SKOV3 cells and 40% in OVCAR3 cells, and migration ability was inhibited by 73% in SKOV3 cells and 62% in OVCAR3 cells after MIR4697HG knockdown. MIR4697HG knockdown also caused a decrease in matrix metalloprotease-9, phosphorylated ERK, and phosphorylated AKT. These data suggested that MIR4697HG promoted ovarian cancer growth and metastasis. The aggressive role of MIR4697HG in ovarian cancer may be related to the ERK and AKT signaling pathways.

Indexed as

AnimalsCell Line, TumorCell MovementCell ProliferationFemaleGene Knockdown TechniquesHeterograftsHumansMAP Kinase Signaling SystemMatrix Metalloproteinase 9MiceMice, NudeNeoplasm InvasivenessNeoplasm MetastasisOvarian NeoplasmsProto-Oncogene Proteins c-aktMatrix Metalloproteinase 9MMP9 protein, humanProto-Oncogene Proteins c-aktRNA, Long NoncodingRNA, Neoplasm

Identifiers

PMID28168162
PMCPMC5259593
OpenAlexW2571047848

What OpenQuestion holds

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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.