Evidence map›Paper›PMID 27819058›Full record

ArticleACS sensors2016

Insulin promoter-driven Gaussia luciferase-based insulin secretion biosensor assay for discovery of β-cell glucose-sensing pathways.

Michael A Kalwat, Chonlarat Wichaidit, Alejandra Y Nava Garcia, Melissa K McCoy, Kathleen McGlynn, In Hyun Hwang, John B MacMillan, Bruce A Posner, Melanie H Cobb

Abstract read
In one paragraph

Article in ACS sensors, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  13. Article
  14. Small-molecule discovery in the pancreatic beta cell.Current opinion in chemical biology · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. High-Throughput Screening for Insulin Secretion Modulators.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  19. Emerging biosensors in detection of natural products.Synthetic and systems biotechnology · 2020
    Review
  20. Article
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

9 authors at 3 institutions in 1 country.

Michael A KalwatDepartment of Phamacology, UT Southwestern Medical Center, Dallas, TX 75235, USA.
Chonlarat WichaiditDepartment of Phamacology, UT Southwestern Medical Center, Dallas, TX 75235, USA.
Alejandra Y Nava GarciaDepartment of Phamacology, UT Southwestern Medical Center, Dallas, TX 75235, USA.
Melissa K McCoyDepartment of Biochemistry, UT Southwestern Medical Center, Dallas, TX 75235, USA.
Kathleen McGlynnDepartment of Phamacology, UT Southwestern Medical Center, Dallas, TX 75235, USA.
In Hyun HwangDepartment of Biochemistry, UT Southwestern Medical Center, Dallas, TX 75235, USA.
John B MacMillanDepartment of Biochemistry, UT Southwestern Medical Center, Dallas, TX 75235, USA.
Bruce A PosnerDepartment of Biochemistry, UT Southwestern Medical Center, Dallas, TX 75235, USA.
Melanie H CobbDepartment of Phamacology, UT Southwestern Medical Center, Dallas, TX 75235, USA.
The University of Texas Southwestern Medical Center · USSouthwestern Medical CenterSouthwestern Medical Center · US

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Sandi Leigh Pruitt · 2010 to 2026
$53.7M
Urgent Covid-19 Revision to the Center for High-Throughput Functional Annotation of Natural ProductsU41AT008718 · NCCIH · UT SOUTHWESTERN MEDICAL CENTER · PI CECH, NADJA B, LININGTON, ROGER G · 2015 to 2024
$10.1M
MAP Kinse in Islet FunctionR01DK055310 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI COBB, MELANIE H. · 1998 to 2014
$3.4M
Role of isoxazole compounds in beta cell differentiation and functionF32DK100113 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI KALWAT, MICHAEL ANDREW · 2013 to 2016
$161k
NCCIH NIH HHS U41 AT008718NCI NIH HHS P30 CA142543NIDDK NIH HHS F32 DK100113NIDDK NIH HHS R01 DK055310
6 · The paper itself

Abstract

High throughput screening of insulin secretion is intractable with current methods. We developed a secreted insulin-luciferase system (Ins-GLuc) in β cells that is rapid, inexpensive, and amenable to 96- and 384-well formats. We treated stable Ins-GLuc-expressing MIN6 cells overnight with 6298 marine natural product fractions. The cells were then washed to remove media and chemicals, followed by stimulation with glucose in the diazoxide paradigm. These conditions allowed the discovery of many insulin secretion suppressors and potentiators. The mechanisms of action of these natural products must be long-lasting given the continuance of secretory phenotypes in the absence of chemical treatment. We anticipate that these natural products and their target pathways will lead to a greater understanding of glucose-stimulated insulin secretion.

Indexed as

Gaussiahigh-throughput screeninginsulinpancreatic islet beta cell marine natural products.

Identifiers

PMID27819058
PMCPMC5089812
OpenAlexW2530758423

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.