Evidence map›Paper›PMID 19192212›Full record

ArticlePigment cell & melanoma research2009

Mitf dosage as a primary determinant of melanocyte survival after ultraviolet irradiation.

Thomas J Hornyak, Shunlin Jiang, Esther A Guzmán, Beth N Scissors, Chinisada Tuchinda, Hongbin He, James D Neville, Faith M Strickland

Open access · greenAbstract read
In one paragraph

Article in Pigment cell & melanoma research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 34 citations in OpenAlex.

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  10. Isolating primary melanocyte-like cells from the mouse heart.Journal of visualized experiments : JoVE · 2014
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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

8 authors at 2 institutions in 1 country.

Thomas J HornyakDermatology Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, USA.
Shunlin Jiang
Esther A Guzmán
Beth N Scissors
Chinisada Tuchinda
Hongbin He
James D Neville
Faith M Strickland
Henry Ford Health System · USCenter for Cancer Research · US

Funding

Ras Signalling in Human MelanomaZ01BC010565 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HORNYAK, THOMAS J · 2004 to 2008
$1.1M
Transcriptional Regulation of Melanocyte DevelopmentR01AR047951 · NIAMS · HENRY FORD HEALTH SYSTEM · PI STRICKLAND, FAITH M · 2001 to 2004
$969k
Regulation of Melanocyte Development and DifferentiationZIABC010479 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HORNYAK, THOMAS J · 2009 to 2012
$289k
Regulation of Melanocyte Development and DifferentiationZ01BC010479 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HORNYAK, THOMAS J · 2003 to 2008
$223k
LINEAGE DETERMINATION IN NEURAL CREST DEVELOPMENTK08AR001992 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI HORNYAK, THOMAS J · 1996 to 2000
$115k
Intramural NIH HHS Z01 BC010479Intramural NIH HHS Z01 BC010565NIAMS NIH HHS K08 AR01992NIAMS NIH HHS R01 AR047951NIAMS NIH HHS R01-AR47951
6 · The paper itself

Abstract

Microphthalmia-associated transcription factor (Mitf) is essential for melanocyte development and function and regulates anti-apoptotic Bcl2 expression. We hypothesized that cellular deficiency of Mitf can influence melanocyte survival in response to ultraviolet (UV) radiation. Primary melanocyte cultures were prepared from neonatal wild-type mice and congenic animals heterozygous for Mitf mutations Mitf (mi-vga9/+) and Mitf(Mi-wh/+) and exposed to UV irradiation. Wild-type melanocytes were more resistant to UV-induced apoptosis than melanocytes partially deficient in Mitf activity, as determined by relative levels of intracellular melanin and relative activation of Mitf target genes Tyr, Tyrp1, Dct, and Cdk2. Comparative experiments with wild-type cells and congenic albino melanocytes demonstrated that these differences are not due to differences in melanin content, implicating Mitf as a primary determinant of UV-dependent melanocyte survival. Mitf activity correlated directly with resistance to UV-induced apoptosis in melanocytes. Mitf was important not only for regulating the expression of anti-apoptotic Bcl-2 following UV irradiation, but also the expression of the pro-apoptotic BH3-only Bad protein and activation of the extrinsic apoptotic pathway. Hence, Mitf is a multifaceted regulator of UV-induced apoptosis in melanocytes.

Indexed as

Gene DosageMicrophthalmia-Associated Transcription FactorUltraviolet RaysAnimalsApoptosisCells, CulturedGene Expression RegulationHair ColorMelaninsMelanocytesMiceMice, Inbred C57BLMutationMelaninsMicrophthalmia-Associated Transcription Factor

Identifiers

PMID19192212
PMCPMC6980044
OpenAlexW2124173513

What OpenQuestion holds

Textmetadata
LicenceTDM
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.