Evidence map›Paper›PMID 28215840›Full record

ArticleGynecologic oncology2017

Cytidine deaminase Apobec3a induction in fallopian epithelium after exposure to follicular fluid.

Pavla Brachova, Nehemiah S Alvarez, Bradley J Van Voorhis, Lane K Christenson

Abstract read
In one paragraph

Article in Gynecologic oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 11 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

4 authors at 2 institutions in 1 country.

Pavla BrachovaDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160, United States. Electronic address: pbrachova@kumc.edu.
Nehemiah S AlvarezDepartment of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS 66160, United States. Electronic address: nalvarez@kumc.edu.
Bradley J Van VoorhisDepartment of Obstetrics and Gynecology, University of Iowa, Iowa City, IA 52242, United States. Electronic address: brad-van-voorhis@uiowa.edu.
Lane K ChristensonDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160, United States. Electronic address: lchristenson@kumc.edu.
University of Kansas Medical Center · USUniversity of Iowa · US

Funding

Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI NICOLE L NOLLEN · 2012 to 2026
$40.1M
Exosome / microvesicle regulation of oocyte developmental competenceR21HD082484 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI CHRISTENSON, LANE K., MCGINNIS, LYNDA K. · 2015 to 2016
$413k
Role of Follicular Fluid Exosomes on Ovarian/Fallopian CarcinogenesisF32CA200357 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BRACHOVA, PAVLA · 2016 to 2017
$118k
NCI NIH HHS F32 CA200357NCI NIH HHS P30 CA168524NICHD NIH HHS R21 HD082484
6 · The paper itself

Abstract

objectiveOvarian carcinomas that originate from fallopian epithelial cells are suggested to arise due to repeated exposure to ovulatory follicular fluid (FF). Mechanistic explanation(s) for how this occurs are unknown. Here, we sought to understand if FF exposure to fallopian epithelial cells could induce DNA damage and expression of a known family of DNA mutators, apolipoprotein B mRNA editing enzyme, catalytic polypeptide (APOBEC) cytidine deaminases.

methodsFollicular fluid and matched patient plasma samples were obtained from donors. Fallopian epithelial cells (FT33-TAg, FT189, FT190, and FT194) were cultured with FF or plasma for 24h, and cell proliferation and DNA damage were assessed. Effects of FF on Apobec gene expression were determined by qRT-PCR and western blot analyses. Fallopian epithelial cells were transfected with an APOBEC3A expression vector and DNA damage was assessed.

resultsFollicular fluid exposure increased epithelial cell proliferation as measured by three independent methods, and DNA damage accumulation as assessed using three independent measures. This effect was specific to FF, as matched patient plasma did not have the same effects. Increased expression of Apobec3a was observed in fallopian epithelial cells following exposure to 5 of 8 patient FF samples, and transient overexpression of APOBEC3A was sufficient to induce double strand DNA breaks.

conclusionsFollicular fluid can induce cell proliferation and DNA damage accumulation in cultured fallopian epithelial cells. Increased expression of APOBEC3A, a known DNA mutator, may explain the high incidence of DNA damage after FF exposure. The role of Apobec3a in ovulation-induced inflammation warrants further investigation.

Indexed as

AdultCell ProliferationCytidine DeaminaseDNA Breaks, Double-StrandedEnzyme InductionEpithelial CellsFallopian TubesFemaleFollicular FluidGene ExpressionHumansOvarian NeoplasmsProteinsRNA, MessengerYoung AdultAPOBEC3A protein, humanCytidine DeaminaseProteinsRNA, MessengerApobecDNA damageFallopian tubeFollicular fluidOvarian cancerOvulation

Identifiers

PMID28215840
PMCPMC5447478
OpenAlexW2588105995

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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.