Evidence map›Paper›PMID 36499183›Full record

ArticleInternational journal of molecular sciences2022

miR-18a-5p Is Involved in the Developmental Origin of Prostate Cancer in Maternally Malnourished Offspring Rats: A DOHaD Approach.

Sergio Alexandre Alcantara Santos, Luiz Marcos Frediani Portela, Ana Carolina Lima Camargo, Flavia Bessi Constantino, Ketlin Thassiani Colombelli, Matheus Naia Fioretto, Renato Mattos, Bruno Evaristo de Almeida Fantinatti, Michela Alessandra Denti, Silvano Piazza and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 8 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

13 authors at 4 institutions in 4 countries.

Sergio Alexandre Alcantara SantosDepartment of Structural and Functional Biology, Institute of Biosciences, Sao Paulo State University (UNESP), Unesp Botucatu, Botucatu 18618-689, SP, Brazil.ORCID 0000-0002-1375-1634
Luiz Marcos Frediani PortelaDepartment of Structural and Functional Biology, Institute of Biosciences, Sao Paulo State University (UNESP), Unesp Botucatu, Botucatu 18618-689, SP, Brazil.
Ana Carolina Lima CamargoDepartment of Structural and Functional Biology, Institute of Biosciences, Sao Paulo State University (UNESP), Unesp Botucatu, Botucatu 18618-689, SP, Brazil.
Flavia Bessi ConstantinoDepartment of Structural and Functional Biology, Institute of Biosciences, Sao Paulo State University (UNESP), Unesp Botucatu, Botucatu 18618-689, SP, Brazil.ORCID 0000-0002-8831-325X
Ketlin Thassiani ColombelliDepartment of Structural and Functional Biology, Institute of Biosciences, Sao Paulo State University (UNESP), Unesp Botucatu, Botucatu 18618-689, SP, Brazil.
Matheus Naia FiorettoDepartment of Structural and Functional Biology, Institute of Biosciences, Sao Paulo State University (UNESP), Unesp Botucatu, Botucatu 18618-689, SP, Brazil.
Renato MattosDepartment of Structural and Functional Biology, Institute of Biosciences, Sao Paulo State University (UNESP), Unesp Botucatu, Botucatu 18618-689, SP, Brazil.
Bruno Evaristo de Almeida FantinattiDepartment of Structural and Functional Biology, Institute of Biosciences, Sao Paulo State University (UNESP), Unesp Botucatu, Botucatu 18618-689, SP, Brazil.ORCID 0000-0002-2126-3438
Michela Alessandra DentiDepartment of Cellular, Computational and Integrative Biology-CIBIO, University of Trento, 38123 Trento, Italy.ORCID 0000-0001-7203-7062
Silvano PiazzaDepartment of Cellular, Computational and Integrative Biology-CIBIO, University of Trento, 38123 Trento, Italy.ORCID 0000-0002-7156-5434
Sérgio Luis FelisbinoDepartment of Structural and Functional Biology, Institute of Biosciences, Sao Paulo State University (UNESP), Unesp Botucatu, Botucatu 18618-689, SP, Brazil.ORCID 0000-0002-6870-5192
Elena ZambranoDepartamento de Biología de la Reproducción, Instituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico City 14080, Mexico.ORCID 0000-0002-0362-9117
Luis Antonio JustulinDepartment of Structural and Functional Biology, Institute of Biosciences, Sao Paulo State University (UNESP), Unesp Botucatu, Botucatu 18618-689, SP, Brazil.ORCID 0000-0001-6142-3515
Universidade Estadual Paulista (Unesp) · BRUniversity of Trento · ITFox Chase Cancer Center · USInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MX

Funding

National Council for Scientific and Technological Development CNPq grant # 310663/ 2018- 0São Paulo Research Foundation 2017/01063-7São Paulo Research Foundation 2017/25198-9São Paulo Research Foundation 2019/03121-0
6 · The paper itself

Abstract

The Developmental Origins of Health and Disease (DOHaD) concept correlates early life exposure to stressor conditions with the increased incidence of non-communicable chronic diseases, including prostate cancer (PCa), throughout the life span. However, the molecular mechanisms involved in this process remain poorly understood. In this study, the deregulation of two miRNAs (rno-miR-18a-5p and rno-miR-345-3p) was described in the ventral prostate VP of old rats born to dams fed with a low protein diet (LPD) (6% protein in the diet) during gestational and lactational periods. Integrative analysis of the (VP) transcriptomic and proteomic data revealed changes in the expression profile of 14 identified predicted targets of these two DE miRNAs, which enriched terms related to post-translational protein modification, metabolism of proteins, protein processing in endoplasmic reticulum, phosphonate and phosphinate metabolism, the calnexin/calreticulin cycle, metabolic pathways, N-glycan trimming in the ER and the calnexin/calreticulin cycle, hedgehog ligand biogenesis, the ER-phagosome pathway, detoxification of reactive oxygen species, antigenprocessing-cross presentation, RAB geranylgeranylation, collagen formation, glutathione metabolism, the metabolism of xenobiotics by cytochrome P450, and platinum drug resistance. RT-qPCR validated the deregulation of the miR-18a-5p/P4HB (prolyl 4-hydroxylase subunit beta) network in the VP of older offspring as well as in the PNT-2 cells transfected with mimic miR-18a-5p. Functional in vitro studies revealed a potential modulation of estrogen receptor α (ESR1) by miR-18a-5p in PNT-2 cells, which was also confirmed in the VP of older offspring. An imbalance of the testosterone/estrogen ratio was also observed in the offspring rats born to dams fed with an LPD. In conclusion, deregulation of the miR-18a-5p/P4HB network can contribute to the developmental origins of prostate cancer in maternally malnourished offspring, highlighting the need for improving maternal healthcare during critical windows of vulnerability early in life.

Indexed as

MicroRNAsProstatic NeoplasmsAnimalsGene Expression ProfilingMaleProteomicsRatsTranscriptomeMicroRNAsagingDevelopmental Origins of Health and Disease (DOHaD)epigeneticsmiR-18a-5p/P4HB networkprostate cancer

Identifiers

PMID36499183
PMCPMC9739077
OpenAlexW4310375996

What OpenQuestion holds

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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.