Evidence map›Paper›PMID 32931357›Full record

ArticleCell cycle (Georgetown, Tex.)2020

Elevated microRNA-7 inhibits proliferation and tumor angiogenesis and promotes apoptosis of gastric cancer cells via repression of Raf-1.

Jing Lin, Zewa Liu, Shasha Liao, E Li, Xiaohua Wu, Wanting Zeng

RetractedOpen access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  7. Downregulation of miR‑7 and miR‑153 is involved inInternational journal of oncology · 2023
    Article
  8. Article
  9. Review
  10. Host miRNAs-microbiota interactions in gastric cancer.Journal of translational medicine · 2022
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Jing LinOncology Department, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.
Zewa LiuOncology Department, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.
Shasha LiaoOncology Department, Shantou Longhu People's Hospital , Shantou, Guangdong, China.
E LiOncology Department, Shantou Longhu People's Hospital , Shantou, Guangdong, China.
Xiaohua WuOncology Department, Shantou Longhu People's Hospital , Shantou, Guangdong, China.
Wanting ZengMSci Applied Medical Science, Division of Medicine, University College London, London, WC1E 6BT, United Kingdom.
First Affiliated Hospital of Shantou University Medical College · CNYue Bei People's Hospital · CNShantou University · CNUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSince the essential involvement of microRNAs (miRNAs) in the development and progression of GC, the study was for the exploration of the value of microRNA-7 (miR-7) in the evaluation of neoadjuvant chemotherapy for gastric cancer (GC) and its effects on apoptosis, proliferation and angiogenesis of GC.

methodsmiR-7 expression in serum of GC patients before and after neoadjuvant chemotherapy were detected to explore its role in neoadjuvant chemotherapy of GC. The GC cells were transfected with miR-7 mimics/inhibitors, or siRNA-Raf-1 to figure out their roles in proliferation, migration, invasion, cycle distribution and apoptosis. Tumor xenograft was conducted to test tumor growth. Microvessel density (MVD) in tumors was tested by immunohistochemical staining.

resultsmiR-7 expression in serum of GC patients was lower than that of healthy controls while it was elevated after neoadjuvant chemotherapy. Moreover, higher miR-7 expression was exhibited in chemotherapy-effective patients rather than chemotherapy-ineffective patients (

conclusionOur study highlights that elevated miR-27a indicates the good efficacy of neoadjuvant chemotherapy in GC and miR-7 targets Raf-1 to suppress tumor development and angiogenesis of GC cells.

Indexed as

ApoptosisCell ProliferationNeovascularization, PathologicAdultAgedAnimalsCase-Control StudiesCell Line, TumorCell MovementChemotherapy, AdjuvantFemaleGene Expression Regulation, NeoplasticHumansMaleMice, Inbred BALB CMice, NudeMicroRNAsMIRN7-1 microRNA, humanProto-Oncogene Proteins c-rafRaf1 protein, humanapoptosisgastric cancerinvasionMicroRNA-7migrationneoadjuvant chemotherapyproliferationRaf-1

Identifiers

PMID32931357
PMCPMC7553585
OpenAlexW3087502936

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.