Evidence map›Paper›PMID 33008590›Full record

ArticleBiochemical and biophysical research communications2020

Characterisation of progestins used in hormonal contraception and progesterone via the progesterone receptor.

Kim Enfield, Meghan Cartwright, Renate Louw-du Toit, Chanel Avenant, Donita Africander, Janet P Hapgood

Abstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2020. 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
–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

6 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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.

Kim EnfieldDepartment of Molecular and Cell Biology, University of Cape Town, Private Bag X3, Rondebosch, Cape Town, 7700, South Africa. Electronic address: enfkim001@myuct.ac.za.
Meghan CartwrightDepartment of Biochemistry, Stellenbosch University, Private Bag X1, Matieland, 7602, South Africa. Electronic address: meghanc@sun.ac.za.
Renate Louw-du ToitDepartment of Biochemistry, Stellenbosch University, Private Bag X1, Matieland, 7602, South Africa. Electronic address: renate@sun.ac.za.
Chanel AvenantDepartment of Molecular and Cell Biology, University of Cape Town, Private Bag X3, Rondebosch, Cape Town, 7700, South Africa. Electronic address: avncha002@gmail.com.
Donita AfricanderDepartment of Biochemistry, Stellenbosch University, Private Bag X1, Matieland, 7602, South Africa. Electronic address: drho@sun.ac.za.
Janet P HapgoodDepartment of Molecular and Cell Biology, University of Cape Town, Private Bag X3, Rondebosch, Cape Town, 7700, South Africa; Institute of Infectious Disease and Molecular Medicine, University of Cape Town, South Africa. Electronic address: janet.hapgood@uct.ac.za.

Funding

Combination treatment for protection against HIV1 and pregnancyR01HD083026 · NICHD · UNIVERSITY OF CAPE TOWN · PI HAPGOOD, JANET PATRICIA, HEL, ZDENEK · 2015 to 2019
$2.5M
NICHD NIH HHS R01 HD083026
6 · The paper itself

Abstract

Different progestogens are widely used in hormonal therapy and mediate their therapeutic actions via the progesterone receptor (PR). Little published data exist on their relative efficacies and potencies via the PR, while those available may be confounded by off-target receptors, different methodologies and model systems. We performed dose-response analysis to investigate the efficacies and potencies for transcription of progesterone and several progestins widely used in contraception via the B isoform of human PR (PR-B). We compared responses using three different cell lines and two different transient transfection conditions. Results show that in vitro biological responses via PR-B for the select progestogens can vary significantly in biocharacter, rank order and absolute values for efficacies and potencies, depending on the cell line and transfection condition. Progestogen rank orders for published relative binding affinities are mostly different to those for relative efficacies and potencies. These in vitro differences suggest that rank orders and absolute values of the efficacies and potencies of the progestogens are likely to vary in vivo in a cell-specific and progestogen-specific manner, and cannot easily be extrapolated from in vitro data, as is usually the practice. While obtaining such data in vivo is not possible, these in vitro data show proof of concept for likely significant cell- and progestogen-specific PR-B effects.

Indexed as

AnimalsCell Line, TumorChlorocebus aethiopsContraceptive Agents, HormonalCOS CellsHumansProgesteroneProgestinsReceptors, ProgesteroneTranscription, GeneticTransfectionContraceptive Agents, HormonalProgesteroneprogesterone receptor BProgestinsReceptors, ProgesteroneDose-responseEfficacyPotencyProgesteroneProgesterone receptorProgestins

Identifiers

PMID33008590
PMCPMC8129485

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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.