Evidence map›Paper›PMID 33210473›Full record

ArticleCancer medicine2021

MiR-362 suppresses cervical cancer progression via directly targeting BAP31 and activating TGFβ/Smad pathway.

Shuya Yang, Yuanjie Sun, Dongbo Jiang, Jing Wang, Erle Dang, Zichao Li, Jiayi Zhou, Yuchen Lu, Jingqi Shi, Liang Tao and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

24 citing papers in PubMed, 35 citations in OpenAlex.

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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

14 authors at 2 institutions in 1 country.

Shuya YangDepartment of Immunology, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.
Yuanjie SunDepartment of Immunology, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.
Dongbo JiangDepartment of Immunology, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.
Jing WangDepartment of Immunology, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.
Erle DangDepartment of Dermatology, Xijing Hospital, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.
Zichao LiSchool of Basic Medicine, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.
Jiayi ZhouSchool of Basic Medicine, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.
Yuchen LuSchool of Basic Medicine, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.
Jingqi ShiDepartment of Immunology, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.
Liang TaoDepartment of Immunology, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.
Jun WangDepartment of Medical Microbiology and Parasitology, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.
Boquan JinDepartment of Immunology, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.
Lianhe ZhengDepartment of Orthopedics, Tangdu Hospital, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.
Kun YangDepartment of Immunology, The Fourth Military Medical University, Xi'an, Shaanxi, People's Republic of China.ORCID 0000-0003-0305-6256
Air Force Medical University · CNXijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BAP31 (B-cell receptor-associated protein 31) is an important regulator of intracellular signal transduction and highly expressed in several cancer tissues or testicular tissues. Our previous study had revealed that elevated BAP31 plays a crucial role in the progress and metastasis of cervical cancer. Even so, the precise mechanism of abnormal BAP31 elevation in cervical cancer has not been fully elucidated. We revealed that the expression of BAP31 was mainly regulated by microRNA-362 (miR-362), which was markedly downregulated in cervical cancer tissues and negatively correlated with clinical tumor staging. Overexpression of miR-362 inhibited cervical cancer cell proliferation and increased the proportion of apoptotic cells. Furthermore, miR-362 reduced the tumor sizes and prolonged mice survival time in xenograft nude mice model. Finally, we demonstrated that the BAP31/SPTBN1 complex regulated tumor progression through the Smad 2/3 pathway under the control of miR-362. Collectively, our findings demonstrated that miR-362 could work as an anti-oncomiR that inhibits proliferation and promotes apoptosis in cervical cancer cells via BAP31 and TGFβ/Smad pathway. Overexpression of miR-362 might be a potential therapeutic strategy for cervical cancer.

Indexed as

AnimalsApoptosisCell ProliferationDisease ProgressionFemaleGene Expression Regulation, NeoplasticHeLa CellsHumansMembrane ProteinsMiceMice, NudeMicroRNAsSignal TransductionSmad2 ProteinSmad3 ProteinTransforming Growth Factor betaBCAP31 protein, humanMembrane ProteinsMicroRNAsMIRN362 microRNA, humanSmad2 ProteinSMAD2 protein, humanSmad3 ProteinSMAD3 protein, humanTransforming Growth Factor betaanti-oncomiRBAP31cervical cancermiR-362TGFβ/Smad pathway

Identifiers

PMID33210473
PMCPMC7826455
OpenAlexW3100634768

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.