Evidence map›Paper›PMID 37907650›Full record

ArticleDiscover oncology2023

Down-regulation of DPP4 by TGFβ1/miR29a-3p inhibited proliferation and promoted migration of ovarian cancer cells.

Chong Liu, Zhao-Wei Gao, Ying-Qi Liu, Lan Yang, Xia-Nan Wu, Ke Dong, Xiao-Ming Zhu

Open access · goldAbstract read
In one paragraph

Article in Discover oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 7 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

7 authors at 3 institutions in 1 country.

Chong Liu *Department of Clinical Diagnosis, Tangdu Hospital, Air Force Military Medical University, Xinsi Road, Xi'an, 710038, China.
Zhao-Wei Gao *Department of Clinical Diagnosis, Tangdu Hospital, Air Force Military Medical University, Xinsi Road, Xi'an, 710038, China.
Ying-Qi LiuSchool of Basic Medical Sciences, Air Force Medical University, No. 4 Company, Xi'an, China.
Lan YangDepartment of Clinical Diagnosis, Tangdu Hospital, Air Force Military Medical University, Xinsi Road, Xi'an, 710038, China.
Xia-Nan WuDepartment of Clinical Diagnosis, Tangdu Hospital, Air Force Military Medical University, Xinsi Road, Xi'an, 710038, China.
Ke DongDepartment of Clinical Diagnosis, Tangdu Hospital, Air Force Military Medical University, Xinsi Road, Xi'an, 710038, China. tdjyk3@fmmu.edu.cn.ORCID http://orcid.org/0000-0002-5734-2373
Xiao-Ming ZhuDepartment of Obstetrics and Gynecology, Hainan Branch of PLA General Hospital, Jianglin Road, Sanya, 572022, China. xiaomingzhu1981@hotmail.com.ORCID http://orcid.org/0000-0002-7005-0455
Tang Du Hospital · CNAir Force Engineering University · CNHainan 301 Hospital · CN

Funding

the key RD projects of shanxi province NO.2021SF-005the Scientist Fund of Air Force Medical University NO.2022XC054
6 · The paper itself

Abstract

objectiveTo explore the DPP4 expression changes and functions in ovarian cancer (OV), as well as the regulation mechanism for DDP4.

methodsGEPIA2, GSE18520, GSE26712 and UALCAN were used to analyze differences in DPP4 expression between OV tumors and control tissues. Serum DPP4 levels were measured by ELISA. The prognostic values of DPP4 were evaluated using a Kaplan-Meier (KM) plotter. Small interfering RNA was used for DPP4 knockdown in OVCAR-3 and SKOV-3 cells. CCK-8 and scratch healing assays were used to determine the cells' proliferation and migration abilities. Flow cytometry (FCM) was used to detect the cell cycle and apoptosis. A dual-luciferase assay was designed to confirm the regulatory effect of miR-29a-3p on DPP4.

resultsThe expressions of DPP4 mRNA and protein were decreased in OV tumor tissues. Serum DPP4 levels decreased in OV patients. KM plotter analysis showed correlation between high DPP4 expression and a poor prognosis in OV patients. By targeting knockdown of DPP4, we found that OVCAR-3 and SKOV-3 cells' proliferation was inhibited, while cell's migration ability was significantly promoted. FCM analysis showed that DPP4 knockdown induced a decrease in the S phase. Furthermore, DPP4 was shown to be downregulated by miR-29a-3p and TGFβ1 in OVCAR-3 cells, and miR-29a-3p expression was upregulated by TGFβ1. The effects of miR-29a-3p and TGFβ1 on OVCAR-3 cells' biological behaviors were consistent with DPP4 knockdown.

conclusionDPP4 was downregulated in OV patients. DPP4 knockdown significantly inhibited OVCAR-3 and SKOV-3 cell proliferation and promoted cell migration. DDP4 can be downregulated by TGFβ1 through the upregulation of miR-29a-3p in OV cells.

Indexed as

DPP4MigrationmiR-29a-3pOvarian cancerProliferation

Identifiers

PMID37907650
PMCPMC10618141
OpenAlexW4388070218

What OpenQuestion holds

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LicenceCC BY
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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.