Evidence map›Paper›PMID 28231414›Full record

ArticleCancer science2017

MicroRNA-135a-3p as a promising biomarker and nucleic acid therapeutic agent for ovarian cancer.

Satoshi Fukagawa, Kohei Miyata, Fusanori Yotsumoto, Chihiro Kiyoshima, Sung Ouk Nam, Haruchika Anan, Takahiro Katsuda, Daisuke Miyahara, Masaharu Murata, Hiroshi Yagi and 4 more

Abstract read
In one paragraph

Article in Cancer science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

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

  1. Pooled it
  2. Review
  3. The Role of microRNA in the Prognosis and Diagnosis of Ovarian Cancer.International journal of molecular sciences · 2025
    Review
  4. Review
  5. Article
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  10. Article
  11. Review
  12. The Advances in Epigenetics for Cancer Radiotherapy.International journal of molecular sciences · 2022
    Review
  13. Article
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  17. Article
  18. Modulation of Immune Response toFrontiers in cellular and infection microbiology · 2021
    Article
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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.

Satoshi FukagawaDepartment of Obstetrics and Gynecology, Fukuoka University, Fukuoka, Japan.ORCID http://orcid.org/0000-0002-7154-1512
Kohei MiyataDepartment of Obstetrics and Gynecology, Fukuoka University, Fukuoka, Japan.
Fusanori YotsumotoDepartment of Obstetrics and Gynecology, Fukuoka University, Fukuoka, Japan.
Chihiro KiyoshimaDepartment of Obstetrics and Gynecology, Fukuoka University, Fukuoka, Japan.
Sung Ouk NamDepartment of Obstetrics and Gynecology, Fukuoka University, Fukuoka, Japan.
Haruchika AnanDepartment of Obstetrics and Gynecology, Fukuoka University, Fukuoka, Japan.
Takahiro KatsudaDepartment of Obstetrics and Gynecology, Fukuoka University, Fukuoka, Japan.
Daisuke MiyaharaDepartment of Obstetrics and Gynecology, Fukuoka University, Fukuoka, Japan.
Masaharu MurataDepartment of Obstetrics and Gynecology, Fukuoka University, Fukuoka, Japan.
Hiroshi YagiDepartment of Obstetrics and Gynecology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Kyoko ShirotaDepartment of Obstetrics and Gynecology, Fukuoka University, Fukuoka, Japan.
Shin'ichiro YasunagaCentral Research Institute for Advanced Molecular Medicine, Fukuoka University, Fukuoka, Japan.
Kiyoko KatoDepartment of Obstetrics and Gynecology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Shingo MiyamotoDepartment of Obstetrics and Gynecology, Fukuoka University, Fukuoka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer is the most lethal gynecologic malignancy. Recently, several molecularly targeted anticancer agents have been developed for ovarian cancer; however, its prognosis remains extremely poor. The development of molecularly targeted therapy, as well as companion diagnostics, is required to improve outcomes for patients with ovarian cancer. In this study, to identify microRNAs (miRNAs) involved in the progression of ovarian cancer we analyzed serum miRNAs in patients with ovarian cancer using miRNA array and quantitative RT-PCR and examined the anticancer properties of miRNA expression in ovarian cancer cells. In patients with ovarian cancer, high amount of miR-135a-3p in serum samples was significantly associated with favorable clinical prognosis. The amount of miR-135a-3p was significantly decreased in patients with ovarian cancer compared with patients with ovarian cysts or normal ovaries. In SKOV-3 and ES-2 human ovarian cancer cells, enhanced expression of miR-135a-3p induced drug sensitivity to cisplatin and paclitaxel and suppressed cell proliferation and xenograft tumor growth. These findings suggest that miR-135a-3p may be considered as a biomarker and a therapeutic agent in ovarian cancer.

Indexed as

AnimalsAntineoplastic AgentsBiomarkers, TumorCell Line, TumorCell ProliferationCisplatinFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMiceMicroRNAsMiddle AgedOvarian NeoplasmsPaclitaxelPrognosisAntineoplastic AgentsBiomarkers, TumorCisplatinMicroRNAsMIRN135 microRNA, humanPaclitaxelBiomarkermiR-135a-3pmolecular targetnucleic acid therapyovarian cancer

Identifiers

PMID28231414
PMCPMC5448652

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LicenceCC BY-NC
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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.