Evidence map›Paper›PMID 29857829›Full record

ArticleTissue & cell2018

Correlation of clinical data with fallopian tube specimen immune cells and tissue culture capacity.

Satish Kumar Ramraj, Katie M Smith, Naveena B Janakiram, Coralee Toal, Ankita Raman, Doris Mangiaracina Benbrook

Abstract read
In one paragraph

Article in Tissue & cell, 2018. 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
–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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
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

6 authors.

Satish Kumar RamrajGynecologic Oncology, Stephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE 10th St, BRC1270, Oklahoma City, OK, 73104, United States.
Katie M SmithDepartment of Obstetrics and Gynecology, University of Oklahoma Health Sciences Center, 800 Stanton L Young Blvd Suite 2400, Oklahoma City, OK, 73104, United States.
Naveena B JanakiramDepartment of Hematologic Oncology, University of Oklahoma Health Sciences Center, 975 NE 10th St, BRC, 1205, Oklahoma City, OK, 73104, United States.
Coralee ToalUniversity of Oklahoma Medical School, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 73104, United States.
Ankita RamanDepartment of OBGYN, University of Nevada, Las Vegas, NV, 89102, United States.
Doris Mangiaracina BenbrookGynecologic Oncology, Stephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE 10th St, BRC1270, Oklahoma City, OK, 73104, United States; Department of Obstetrics and Gynecology, University of Oklahoma Health Sciences Center, 800 Stanton L Young Blvd Suite 2400, Oklahoma City, OK, 73104, United States. Electronic address: Doris-Benbrook@ouhsc.edu.

Funding

Tissue Pathology Shared ResourceP30CA225520 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Michael S. Businelle · 2018 to 2026
$27.1M
Ovarian Cancer ChemopreventionR01CA196200 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI BENBROOK, DORIS MANGIARACINA · 2015 to 2019
$2.5M
NCI NIH HHS P30 CA225520NCI NIH HHS R01 CA196200
6 · The paper itself

Abstract

Human fallopian tube fimbria secretory epithelial cells (hFTSECs) are considered an origin of ovarian cancer and methods for their culture from fallopian tube specimens have been reported. Our objective was to determine whether characteristics of the donors or surgeries were associated with the capacities of fimbria specimens to generate hFTSEC cultures or their immune profiles. There were no surgical complications attributable to fallopian tube removal. Attempts to establish primary hFTSEC cultures were successful in 37 of 55 specimens (67%). Success rates did not differ significantly between specimens grouped by patient or surgery characteristics. Established cultures could be revived after cryopreservation and none became contaminated with microorganisms. Two cultures evaluated for long term growth senesced between passages 10 and 15. M1 macrophages were the predominant cell type, while all other immune cells were present at much lower percentages. IL-10 and TGF-β exhibited opposing trends with M1 and M2 macrophages. Plasma IL-10 levels exhibited significant positive correlation with patient age. In conclusion, fallopian tube fimbria specimens exhibit a pro-inflammatory phenotype and can be used to provide a source of hFTSECs that can be cultured for a limited time regardless of the donor patient age or race, or the type of surgery performed.

Indexed as

AdultAgedCarcinoma, Ovarian EpithelialCell Culture TechniquesCell Line, TumorEpithelial CellsFallopian TubesFemaleHumansMiddle AgedNeoplasms, Glandular and EpithelialOvarian NeoplasmsSalpingectomySpecimen HandlingCytokinesFallopian tube fimbriaHuman fallopian tube secretory epithelial cell culturesInfiltrating immune cellsSalpingectomy

Identifiers

PMID29857829
PMCPMC5986091

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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.