Evidence map›Paper›PMID 25535830›Full record

ArticleEndocrinology2015

PK11195 effect on steroidogenesis is not mediated through the translocator protein (TSPO).

Lan N Tu, Amy H Zhao, Douglas M Stocco, Vimal Selvaraj

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
  2. STAR/STARD1: A mitochondrial intermembrane space cholesterol shuttle degraded through mitophagy.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  15. Cellular sources of TSPO expression in healthy and diseased brain.European journal of nuclear medicine and molecular imaging · 2021
    Review
  16. Article
  17. Article
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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 3 institutions in 1 country.

Lan N TuDepartment of Animal Science, College of Agriculture and Life Sciences (L.N.T., A.H.Z., V.S.), Cornell University, Ithaca, New York 14853; and Department of Cell Biology and Biochemistry, School of Medicine (D.M.S.), Texas Tech University Health Sciences Center, Lubbock, Texas 79430.
Amy H Zhao
Douglas M Stocco
Vimal Selvaraj
New York State College of Agriculture & Life Sciences · USCornell University · USTexas Tech University Health Sciences Center · US

Funding

MITOCHONDRIAL PROTEINS AND LEYDIG CELL STEROIDOGENESISR37HD017481 · NICHD · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI STOCCO, DOUGLAS M · 1996 to 2005
$1.9M
MITOCHONDRIAL PROTEINS AND LEYDIG CELL STEROIDOGENESISR01HD017481 · NICHD · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI STOCCO, DOUGLAS M · 1985 to 2011
$1.5M
NICHD NIH HHS HD-17481NICHD NIH HHS R01 HD017481NICHD NIH HHS R37 HD017481
6 · The paper itself

Abstract

Translocator protein (TSPO) is a mitochondrial outer membrane protein of unknown function with high physiological expression in steroidogenic cells. Using TSPO gene-deleted mice, we recently demonstrated that TSPO function is not essential for steroidogenesis. The first link between TSPO and steroidogenesis was established in studies showing modest increases in progesterone production by adrenocortical and Leydig tumor cell lines after treatment with PK11195. To reconcile discrepancies between physiological and pharmacological interpretations of TSPO function, we generated TSPO-knockout MA-10 mouse Leydig tumor cells (MA-10:TspoΔ/Δ) and examined their steroidogenic potential after exposure to either dibutyryl-cAMP or PK11195. Progesterone production in MA-10:TspoΔ/Δ after dibutyryl-cAMP was not different from control MA-10:Tspo+/+ cells, confirming that TSPO function is not essential for steroidogenesis. Interestingly, when treated with increasing concentrations of PK11195, both control MA-10:Tspo+/+ cells and MA-10:TspoΔ/Δ cells responded in a similar dose-dependent manner showing increases in progesterone production. These results show that the pharmacological effect of PK11195 on steroidogenesis is not mediated through TSPO.

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorClustered Regularly Interspaced Short Palindromic RepeatsDose-Response Relationship, DrugGene DeletionIsoquinolinesLeydig Cell TumorMiceReceptors, GABAAntineoplastic AgentsBzrp protein, mouseIsoquinolinesPK 11195Receptors, GABA

Identifiers

PMID25535830
PMCPMC4330312
OpenAlexW1990064835

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.