Metabolomics reveals that dietary xenoestrogens alter cellular metabolism induced by palbociclib/letrozole combination cancer therapy

Recently, the palbociclib/letrozole combination therapy was granted accelerated US FDA approval for the treatment of estrogen receptor (ER)-positive breast cancer. Since the underlying metabolic effects of these drugs are yet unknown, we investigated their synergism at the metabolome level in MCF-7...

Full description

Saved in:
Bibliographic Details
Main Authors: Warth, Benedikt, Raffeiner, Philipp, Granados, Ana, Huan, Tao, Fang, Mingliang, Forsberg, Erica M., Benton, H. Paul, Goetz, Laura, Johnson, Caroline H., Siuzdak, Gary
Other Authors: School of Civil and Environmental Engineering
Format: Article
Language:English
Published: 2020
Subjects:
Online Access:https://hdl.handle.net/10356/139116
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-139116
record_format dspace
spelling sg-ntu-dr.10356-1391162020-05-15T08:34:14Z Metabolomics reveals that dietary xenoestrogens alter cellular metabolism induced by palbociclib/letrozole combination cancer therapy Warth, Benedikt Raffeiner, Philipp Granados, Ana Huan, Tao Fang, Mingliang Forsberg, Erica M. Benton, H. Paul Goetz, Laura Johnson, Caroline H. Siuzdak, Gary School of Civil and Environmental Engineering Science::Biological sciences Combinatory Chemotherapy Ibrance Recently, the palbociclib/letrozole combination therapy was granted accelerated US FDA approval for the treatment of estrogen receptor (ER)-positive breast cancer. Since the underlying metabolic effects of these drugs are yet unknown, we investigated their synergism at the metabolome level in MCF-7 cells. As xenoestrogens interact with the ER, we additionally aimed at deciphering the impact of the phytoestrogen genistein and the estrogenic mycotoxin zearalenone. A global metabolomics approach was applied to unravel metabolite and pathway modifications. The results clearly showed that the combined effects of palbociclib and letrozole on cellular metabolism were far more pronounced than that of each agent alone and potently influenced by xenoestrogens. This behavior was confirmed in proliferation experiments and functional assays. Specifically, amino acids and central carbon metabolites were attenuated, while higher abundances were observed for fatty acids and most nucleic acid-related metabolites. Interestingly, exposure to model xenoestrogens appeared to counteract these effects. 2020-05-15T08:34:14Z 2020-05-15T08:34:14Z 2018 Journal Article Warth, B., Raffeiner, P., Granados, A., Huan, T., Fang, M., Forsberg, E. M., . . . Siuzdak, G. (2018). Metabolomics reveals that dietary xenoestrogens alter cellular metabolism induced by palbociclib/letrozole combination cancer therapy. Cell Chemical Biology, 25(3), 291-300. doi:10.1016/j.chembiol.2017.12.010 2451-9456 https://hdl.handle.net/10356/139116 10.1016/j.chembiol.2017.12.010 29337187 2-s2.0-85040322941 3 25 291 300 en Cell Chemical Biology © 2017 Elsevier Ltd. All rights reserved.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic Science::Biological sciences
Combinatory Chemotherapy
Ibrance
spellingShingle Science::Biological sciences
Combinatory Chemotherapy
Ibrance
Warth, Benedikt
Raffeiner, Philipp
Granados, Ana
Huan, Tao
Fang, Mingliang
Forsberg, Erica M.
Benton, H. Paul
Goetz, Laura
Johnson, Caroline H.
Siuzdak, Gary
Metabolomics reveals that dietary xenoestrogens alter cellular metabolism induced by palbociclib/letrozole combination cancer therapy
description Recently, the palbociclib/letrozole combination therapy was granted accelerated US FDA approval for the treatment of estrogen receptor (ER)-positive breast cancer. Since the underlying metabolic effects of these drugs are yet unknown, we investigated their synergism at the metabolome level in MCF-7 cells. As xenoestrogens interact with the ER, we additionally aimed at deciphering the impact of the phytoestrogen genistein and the estrogenic mycotoxin zearalenone. A global metabolomics approach was applied to unravel metabolite and pathway modifications. The results clearly showed that the combined effects of palbociclib and letrozole on cellular metabolism were far more pronounced than that of each agent alone and potently influenced by xenoestrogens. This behavior was confirmed in proliferation experiments and functional assays. Specifically, amino acids and central carbon metabolites were attenuated, while higher abundances were observed for fatty acids and most nucleic acid-related metabolites. Interestingly, exposure to model xenoestrogens appeared to counteract these effects.
author2 School of Civil and Environmental Engineering
author_facet School of Civil and Environmental Engineering
Warth, Benedikt
Raffeiner, Philipp
Granados, Ana
Huan, Tao
Fang, Mingliang
Forsberg, Erica M.
Benton, H. Paul
Goetz, Laura
Johnson, Caroline H.
Siuzdak, Gary
format Article
author Warth, Benedikt
Raffeiner, Philipp
Granados, Ana
Huan, Tao
Fang, Mingliang
Forsberg, Erica M.
Benton, H. Paul
Goetz, Laura
Johnson, Caroline H.
Siuzdak, Gary
author_sort Warth, Benedikt
title Metabolomics reveals that dietary xenoestrogens alter cellular metabolism induced by palbociclib/letrozole combination cancer therapy
title_short Metabolomics reveals that dietary xenoestrogens alter cellular metabolism induced by palbociclib/letrozole combination cancer therapy
title_full Metabolomics reveals that dietary xenoestrogens alter cellular metabolism induced by palbociclib/letrozole combination cancer therapy
title_fullStr Metabolomics reveals that dietary xenoestrogens alter cellular metabolism induced by palbociclib/letrozole combination cancer therapy
title_full_unstemmed Metabolomics reveals that dietary xenoestrogens alter cellular metabolism induced by palbociclib/letrozole combination cancer therapy
title_sort metabolomics reveals that dietary xenoestrogens alter cellular metabolism induced by palbociclib/letrozole combination cancer therapy
publishDate 2020
url https://hdl.handle.net/10356/139116
_version_ 1681056995241623552