Evidence map›Paper›PMID 31165412›Full record

ArticleEndocrine2019

Lineage-dependent role of miR-410-3p as oncomiR in gonadotroph and corticotroph pituitary adenomas or tumor suppressor miR in somatotroph adenomas via MAPK, PTEN/AKT, and STAT3 signaling pathways.

Tomasz M Grzywa, Klaudia Klicka, Beata Rak, Dawid Mehlich, Filip Garbicz, Grzegorz Zieliński, Maria Maksymowicz, Emir Sajjad, Paweł K Włodarski

Open access · hybridAbstract read
In one paragraph

Article in Endocrine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
1.8field-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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 33 citations in OpenAlex.

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  16. Differential microRNA Expression inJournal of clinical medicine · 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

9 authors at 3 institutions in 1 country.

Tomasz M GrzywaCenter for Preclinical Research, The Department of Methodology, Medical University of Warsaw, 1B Banacha Str., 02-097, Warsaw, Poland.ORCID 0000-0002-1809-248X
Klaudia KlickaCenter for Preclinical Research, The Department of Methodology, Medical University of Warsaw, 1B Banacha Str., 02-097, Warsaw, Poland.ORCID 0000-0002-3650-5401
Beata RakCenter for Preclinical Research, The Department of Methodology, Medical University of Warsaw, 1B Banacha Str., 02-097, Warsaw, Poland. beata.rak@wum.edu.pl.ORCID 0000-0002-0289-7136
Dawid MehlichCenter for Preclinical Research, The Department of Methodology, Medical University of Warsaw, 1B Banacha Str., 02-097, Warsaw, Poland.
Filip GarbiczCenter for Preclinical Research, The Department of Methodology, Medical University of Warsaw, 1B Banacha Str., 02-097, Warsaw, Poland.ORCID 0000-0002-5548-1564
Grzegorz ZielińskiThe Department of Neurosurgery, Military Institute of Medicine, 128 Szaserów Str., 04-141, Warsaw, Poland.
Maria MaksymowiczThe Department of Pathology and Laboratory Diagnostics, M. Skłodowska-Curie Memorial Cancer Centre and Institute of Oncology, 5 Roentgena Str., 02-781, Warsaw, Poland.
Emir SajjadCenter for Preclinical Research, The Department of Histology and Embryology, Medical University of Warsaw, 1B Banacha Str., 02-097, Warsaw, Poland.
Paweł K WłodarskiCenter for Preclinical Research, The Department of Methodology, Medical University of Warsaw, 1B Banacha Str., 02-097, Warsaw, Poland.ORCID 0000-0002-0683-1791
Medical University of Warsaw · PLThe Maria Sklodowska-Curie National Research Institute of Oncology · PLWojskowy Instytut Medycyny Lotniczej · PL

Funding

Narodowe Centrum Nauki UMO-2016/23/N/NZ5/02597Warszawski Uniwersytet Medyczny 1M15/PM1/17
6 · The paper itself

Abstract

purposemiR-410-3p plays opposite roles in different cancers and may act as an oncomiR or tumor suppressor miR. The purpose of this study was to assess the role of miR-410-3p in somatotroph, gonadotroph, and corticotroph pituitary adenomas.

methodsTissue samples were obtained from 75 patients with pituitary adenoma. miR-410-3p expression was assessed using qRT-PCR performed on RNA isolated from fresh frozen samples. In vitro experiments were performed on cell lines derived from somatotroph (GH3), gonadotroph (RC-4B/C), and corticotroph (AtT-20) pituitary tumors. Cells were transfected with synthetic mimic of miR-410-3p or non-targeting scrambled-miR control. Subsequently, proliferation assays and transwell invasion assays were performed. The expression of cyclin D1, E1, and B1 in cells after transfection was determined using qRT-PCR. The activation of MAPK, PTEN/AKT and STAT3 signaling pathways were assessed using western blot.

resultsWe have found that the level of expression of miR-410-3p differs in particular types of pituitary adenomas. miR-410-3p significantly upregulates proliferation and invasiveness of RC-4B/C and AtT-20 cells, while inhibiting GH3 cells. We observed that the levels of cyclin B1 upon transfection with miR-410-3p mimic were increased in RC-4B/C and AtT-20, yet decreased in GH3 cells. We have shown that miR-410-3p promoted the activation of MAPK, PTEN/AKT, and STAT3 signaling pathways in RC-4B/C and AtT-20 cells, but suppressed their activity in GH3 cells.

conclusionsmiR-410-3p acts as an oncomiR in gonadotroph and corticotroph adenoma cells, while as a tumor suppressor miR in somatotroph adenoma cells.

Indexed as

ACTH-Secreting Pituitary AdenomaCell Line, TumorCell ProliferationCyclinsGonadotropinsGrowth Hormone-Secreting Pituitary AdenomaHumansMicroRNAsMitogen-Activated Protein KinasesNeoplasm InvasivenessOncogene Protein v-aktPituitary NeoplasmsPTEN PhosphohydrolaseSignal TransductionSTAT3 Transcription FactorCyclinsGonadotropinsMicroRNAsMIRN410 microRNA, humanMitogen-Activated Protein KinasesOncogene Protein v-aktPTEN PhosphohydrolasePTEN protein, humanSTAT3 protein, humanSTAT3 Transcription FactorInvasivenessMicroRNAmiR-410-3pPituitary adenomaProliferationPTEN

Identifiers

PMID31165412
PMCPMC6717603
OpenAlexW2948560532

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.