Evidence map›Paper›PMID 32527205›Full record

ArticleTechnology in cancer research & treatment

MicroRNA-96-5p Facilitates the Viability, Migration, and Invasion and Suppresses the Apoptosis of Cervical Cancer Cells byNegatively Modulating SFRP4.

Huiling Zhang, Ruxin Chen, Jinyan Shao

RetractedAbstract readRetracted Publication
In one paragraph

Article in Technology in cancer research & treatment. 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 It has been retracted, and should not be counted.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 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Mechanisms of GPM6A in Malignant Tumors.Cancer reports (Hoboken, N.J.) · 2025
    Review
  7. Article
  8. Frontiers in molecular neuroscience · 2024
    Article
  9. Article
  10. MicroRNA-96: A therapeutic and diagnostic tumor marker.Iranian journal of basic medical sciences · 2022
    Review
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Huiling ZhangDepartment of Clinical Laboratory, Huai'an Maternity and Child Health Hospital, Qingjiangpu District, Huaian City, Jiangsu Province, China.
Ruxin ChenDepartment of Obstetrics and Gynecology, Jinan Maternal and Child Health Hospital, Jinan City, Shandong Province, China.
Jinyan ShaoDepartment of Obstetrics and Gynecology, Laishan Branch of Yantai Yuhuangding Hospital, Laishan District, Yantai City, Shandong Province, China.ORCID 0000-0001-5291-2835

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe current study was intended to research the functional role and regulatory mechanism of microRNA-96-5p in the progression of cervical cancer.

methodsMicroRNA-96-5p expression in cervical cancer tissues was assessed by quantitative real-time polymerase chain reaction. The association between microRNA-96-5p expression and clinicopathological features of patients with cervical cancer was analyzed. MTT, flow cytometry, wound healing, and transwell assay were performed to evaluate the viability, apoptosis, migration, and invasion of Hela and SiHa cells. Targetscan, dual-luciferase reporter gene assay, and RNA pull-down analysis were constructed to evaluate the target relationship between microRNA-96-5p and secreted frizzled-related protein 4.

resultsMicroRNA-96-5p was overexpressed in cervical cancer tissues, and microRNA-96-5p expression was markedly associated with the clinical stage and lymph node metastasis of patients with cervical cancer. Overexpressed microRNA-96-5p facilitated the viability, migration, invasion, and inhibited the apoptosis of Hela and SiHa cells, whereas suppression of microRNA-96-5p exerted the opposite trend. Secreted frizzled-related protein 4 was proved to be a target of microRNA-96-5p. Silencing of secreted frizzled-related protein 4 eliminated the anti-tumor effect of microRNA-96-5p on cervical cancer cells.

conclusionsMicroRNA-96-5p facilitated the viability, migration, and invasion and inhibited the apoptosis of cervical cancer cells via negatively regulating secreted frizzled-related protein 4.

Indexed as

Gene Expression Regulation, NeoplasticAdenocarcinomaApoptosisBiomarkers, TumorCarcinoma, Squamous CellCell MovementCell ProliferationFemaleHumansMicroRNAsMiddle AgedNeoplasm InvasivenessPrognosisProto-Oncogene ProteinsSecreted Frizzled-Related ProteinsTumor Cells, CulturedBiomarkers, TumorMicroRNAsMIRN96 microRNA, humanProto-Oncogene ProteinsSecreted Frizzled-Related ProteinsSFRP4 protein, humancervical cancermigrationmiR-96-5pproliferationSFRP4

Identifiers

PMID32527205
PMCPMC7294480

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Registered trials

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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.