Increased PHGDH expression promotes aberrant melanin accumulation

Abstract Background Copy number gain of the D-3-phosphoglycerate dehydrogenase (PHGDH) gene, which encodes the first enzyme in serine biosynthesis, is found in some human cancers including a subset of melanomas. Methods In order to study the effect of increased PHGDH expression in tissues in vivo, w...

Full description

Bibliographic Details
Main Authors: Katherine R. Mattaini, Mark R. Sullivan, Allison N. Lau, Brian P. Fiske, Roderick T. Bronson, Matthew G. Vander Heiden
Format: Article
Language:English
Published: BMC 2019-07-01
Series:BMC Cancer
Online Access:http://link.springer.com/article/10.1186/s12885-019-5933-5
_version_ 1819049193089531904
author Katherine R. Mattaini
Mark R. Sullivan
Allison N. Lau
Brian P. Fiske
Roderick T. Bronson
Matthew G. Vander Heiden
author_facet Katherine R. Mattaini
Mark R. Sullivan
Allison N. Lau
Brian P. Fiske
Roderick T. Bronson
Matthew G. Vander Heiden
author_sort Katherine R. Mattaini
collection DOAJ
description Abstract Background Copy number gain of the D-3-phosphoglycerate dehydrogenase (PHGDH) gene, which encodes the first enzyme in serine biosynthesis, is found in some human cancers including a subset of melanomas. Methods In order to study the effect of increased PHGDH expression in tissues in vivo, we generated mice harboring a PHGDH tetO allele that allows tissue-specific, doxycycline-inducible PHGDH expression, and we analyzed the phenotype of mice with a ubiquitous increase in PHGDH expression. Results Tissues and cells derived from PHGDH tetO mice exhibit increased serine biosynthesis. Histological examination of skin tissue from PHGDH tetO mice reveals the presence of melanin granules in early anagen hair follicles, despite the fact that melanin synthesis is closely coupled to the hair follicle cycle and does not normally begin until later in the cycle. This phenotype occurs in the absence of any global change in hair follicle cycle timing. The aberrant presence of melanin early in the hair follicle cycle following PHGDH expression is also accompanied by increased melanocyte abundance in early anagen skin. Conclusions These data suggest increased PHGDH expression impacts normal melanocyte biology, but PHGDH expression alone is not sufficient to cause cancer.
first_indexed 2024-12-21T11:28:15Z
format Article
id doaj.art-3c3135e5d5674410bb51cf7b8aa97abe
institution Directory Open Access Journal
issn 1471-2407
language English
last_indexed 2024-12-21T11:28:15Z
publishDate 2019-07-01
publisher BMC
record_format Article
series BMC Cancer
spelling doaj.art-3c3135e5d5674410bb51cf7b8aa97abe2022-12-21T19:05:37ZengBMCBMC Cancer1471-24072019-07-0119111110.1186/s12885-019-5933-5Increased PHGDH expression promotes aberrant melanin accumulationKatherine R. Mattaini0Mark R. Sullivan1Allison N. Lau2Brian P. Fiske3Roderick T. Bronson4Matthew G. Vander Heiden5Koch Institute for Integrative Cancer ResearchKoch Institute for Integrative Cancer ResearchKoch Institute for Integrative Cancer ResearchKoch Institute for Integrative Cancer ResearchRodent Histopathology Core, Harvard Medical School, BostonKoch Institute for Integrative Cancer ResearchAbstract Background Copy number gain of the D-3-phosphoglycerate dehydrogenase (PHGDH) gene, which encodes the first enzyme in serine biosynthesis, is found in some human cancers including a subset of melanomas. Methods In order to study the effect of increased PHGDH expression in tissues in vivo, we generated mice harboring a PHGDH tetO allele that allows tissue-specific, doxycycline-inducible PHGDH expression, and we analyzed the phenotype of mice with a ubiquitous increase in PHGDH expression. Results Tissues and cells derived from PHGDH tetO mice exhibit increased serine biosynthesis. Histological examination of skin tissue from PHGDH tetO mice reveals the presence of melanin granules in early anagen hair follicles, despite the fact that melanin synthesis is closely coupled to the hair follicle cycle and does not normally begin until later in the cycle. This phenotype occurs in the absence of any global change in hair follicle cycle timing. The aberrant presence of melanin early in the hair follicle cycle following PHGDH expression is also accompanied by increased melanocyte abundance in early anagen skin. Conclusions These data suggest increased PHGDH expression impacts normal melanocyte biology, but PHGDH expression alone is not sufficient to cause cancer.http://link.springer.com/article/10.1186/s12885-019-5933-5
spellingShingle Katherine R. Mattaini
Mark R. Sullivan
Allison N. Lau
Brian P. Fiske
Roderick T. Bronson
Matthew G. Vander Heiden
Increased PHGDH expression promotes aberrant melanin accumulation
BMC Cancer
title Increased PHGDH expression promotes aberrant melanin accumulation
title_full Increased PHGDH expression promotes aberrant melanin accumulation
title_fullStr Increased PHGDH expression promotes aberrant melanin accumulation
title_full_unstemmed Increased PHGDH expression promotes aberrant melanin accumulation
title_short Increased PHGDH expression promotes aberrant melanin accumulation
title_sort increased phgdh expression promotes aberrant melanin accumulation
url http://link.springer.com/article/10.1186/s12885-019-5933-5
work_keys_str_mv AT katherinermattaini increasedphgdhexpressionpromotesaberrantmelaninaccumulation
AT markrsullivan increasedphgdhexpressionpromotesaberrantmelaninaccumulation
AT allisonnlau increasedphgdhexpressionpromotesaberrantmelaninaccumulation
AT brianpfiske increasedphgdhexpressionpromotesaberrantmelaninaccumulation
AT rodericktbronson increasedphgdhexpressionpromotesaberrantmelaninaccumulation
AT matthewgvanderheiden increasedphgdhexpressionpromotesaberrantmelaninaccumulation