Evidence map›Paper›PMID 28386361›Full record

ArticleAmerican journal of translational research2017

Downregulation of miR-429 contributes to the development of drug resistance in epithelial ovarian cancer by targeting ZEB1.

Jing Zou, Ling Liu, Qi Wang, Fuqiang Yin, Zhijun Yang, Wei Zhang, Li Li

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 2 syntheses or guidelines pooled it, 71 citations in OpenAlex.

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  13. Autophagy Regulation by Crosstalk between miRNAs and Ubiquitination System.International journal of molecular sciences · 2021
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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 2 institutions in 1 country.

Jing ZouDepartment of Gynecologic Oncology, Affiliated Tumor Hospital of Guangxi Medical University; Laboratory of Early Prevention and Treatment for Regional High Frequence Tumor Ministry of Education Key Laboratory Nanning 530021, Guangxi, P. R. China.
Ling LiuDepartment of Gynecologic Oncology, Affiliated Tumor Hospital of Guangxi Medical University; Laboratory of Early Prevention and Treatment for Regional High Frequence Tumor Ministry of Education Key Laboratory Nanning 530021, Guangxi, P. R. China.
Qi WangDepartment of Gynecologic Oncology, Affiliated Tumor Hospital of Guangxi Medical University; Laboratory of Early Prevention and Treatment for Regional High Frequence Tumor Ministry of Education Key Laboratory Nanning 530021, Guangxi, P. R. China.
Fuqiang YinMedical Scientific Research Centre, Guangxi Medical University Nanning 530021, Guangxi, P. R. China.
Zhijun YangDepartment of Gynecologic Oncology, Affiliated Tumor Hospital of Guangxi Medical University; Laboratory of Early Prevention and Treatment for Regional High Frequence Tumor Ministry of Education Key Laboratory Nanning 530021, Guangxi, P. R. China.
Wei ZhangDepartment of Gynecologic Oncology, Affiliated Tumor Hospital of Guangxi Medical University; Laboratory of Early Prevention and Treatment for Regional High Frequence Tumor Ministry of Education Key Laboratory Nanning 530021, Guangxi, P. R. China.
Li LiDepartment of Gynecologic Oncology, Affiliated Tumor Hospital of Guangxi Medical University; Laboratory of Early Prevention and Treatment for Regional High Frequence Tumor Ministry of Education Key Laboratory Nanning 530021, Guangxi, P. R. China.
Tumor Hospital of Guangxi Medical University · CNGuangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug resistance is an obstacle to the treatment of epithelial ovarian cancer. Recently, research has suggested that miRNAs (microRNAs) are involved in cancer development, and speculation has been made about their possible involvement in drug resistance. Thus, we attempted to identify selected miRNAs involved in the development of chemo-resistance in epithelial ovarian cancer. Using miRNA profiles of a panel of cisplatin-resistant (SKOV3/DDP) cells, we validated data using quantitative real time-PCR (QRT-PCR), and studied the effects of miR-429 on cancer cell chemo-sensitivity, using gain- and loss-of-function studies. Data show that SKOV3/DDP expressed less miR-429 compared with parental SKOV3 cells and lower miR-429 expression conferred shorter overall survival (OS) and less progression-free survival (PFS) than the patients with more miR-429 expression (P < 0.01). Upregulation of miR-429 increases cisplatin sensitivity in epithelial ovarian cancer cells. Studies have confirmed that the zinc finger E-box binding homeobox1 (ZEB1) is a direct and functional target of miR-429 and that over-expression of miR-429 reduces autophagy-related protein anti-ATG7, anti-LC3A/B (P < 0.05). Thus, overexpression of miR-429 may suppress ZEB1, and may be a potential sensitizer to cisplatin treatment that may have therapeutic implications.

Indexed as

Epithelial ovarian cancer miR-429 cisplatin resistance ZEB1

Identifiers

PMID28386361
PMCPMC5376026
OpenAlexW2975803807

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.