Evidence map›Paper›PMID 33185588›Full record

ArticleCancer biomarkers : section A of Disease markers2021

Identification of MYLIP gene and miRNA-802 involved in the growth and metastasis of cervical cancer cells.

Ming Ni, Qin Yan, Hui Xue, Yanfang Du, Shuangdan Zhao, Zhiming Zhao

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 24% 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, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Tumor Necrosis Factor-Mediators of inflammation · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Dysfunction of miR-802 in tumors.Journal of clinical laboratory analysis · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. A novel lncRNA-mRNA-miRNA signature predicts recurrence and disease-free survival in cervical cancer.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2021
    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

6 authors at 4 institutions in 1 country.

Ming NiGynecological Department, Wuhan Hanyang Hospital, Wuhan, Hubei, China.
Qin YanDepartment of Oncology, Chengdu Fifth People's Hospital, Chengdu, Sichuan, China.
Hui XueDepartment of Gynecology, The Qingdao Hiser Hospital, Qingdao, Shandong, China.
Yanfang DuDepartment of Obstetrics and Gynecology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Shuangdan ZhaoDepartment of Obstetrics and Gynecology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Zhiming ZhaoDepartment of Reproductive Medicine, the Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Second Hospital of Hebei Medical University · CNChengdu Fifth People's Hospital · CNQingdao Municipal Hospital · CNWuhan Hankou Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe dysregulation of microRNA-802 (miR-802) has crucial roles in cancer progression. Nevertheless, the bio-function of miR-802 in cervical cancer remains unclear.

objectiveHence, we illuminated the potential roles of miR-802 in cervical cancer cell growth, migration, and invasion.

methodsThe levels of miR-802 and myosin regulatory light chain interacting protein (MYLIP) were measured using qRT-PCR assay. The potential effects of miRNA-802 on cervical cancer cell proliferation and metastatic phenotypes were determined using CCK-8, colony formation, wound healing and Transwell invasion assays. MYLIP was validated as a downstream target gene of miRNA-802 using bioinformatics analysis tool and luciferase report gene assay. The impact of miR-802 on the growth of cervical cancer cell in vivo was analyzed using xenograft model. The expression of MYLIP was measured by western blotting and immunohistochemistry (IHC).

resultsMiRNA-802 was distinctly down-regulated in cervical cancer cells as well as clinical cervical cancer samples. Upregulation of miRNA-802 significantly inhibited the growth and aggressiveness of cervical cancer cell. Additional, MYLIP was a functional target of miR-802. MYLIP was ovrerexpressed in cervical cancer and MYLIP level was negatively associated with the level of miR-802. Overexpression of MYLIP eliminated the inhibitory effects of miR-802 on growth and metastatic-related traits of cervical cancer cell. In vivo, miR-802 also markedly reduced the tumor growth of cervical cancer cell and decreased the expression of MYLIP.

conclusionsMiR-802 inhibits the growth and metastatic-related phenotypes of cervical cancer cell through targeting MYLIP.

Indexed as

Cell Culture TechniquesFemaleHumansMicroRNAsMiddle AgedNeoplasm MetastasisTransfectionUbiquitin-Protein LigasesUterine Cervical NeoplasmsMicroRNAsMIRN802 microRNA, humanMYLIP protein, humanUbiquitin-Protein LigasesCervical cancerinvasionmetastasismiR-802MYLIP

Identifiers

PMID33185588
PMCPMC12499971
OpenAlexW3101154522

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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.