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Subtype-specific circadian clock dysregulation modulates breast cancer biology, invasiveness, and prognosis

Studies in shift workers and model organisms link circadian disruption to breast cancer. However, molecular rhythms in non-cancerous and cancerous human breast tissues are largely unknown. We reconstructed rhythms informatically, integrating locally collected, time-stamped biopsies with public datas...

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Autores principales: Hammarlund, Jan A, Li, Shi-Yang, Wu, Gang, Lian, Jia-wen, Howell, Sacha J, Clarke, Rob, Adamson, Antony, Gonçalves, Cátia F., Hogenesch, John B, Meng, Qing-Jun, Anafi, Ron C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245642/
https://www.ncbi.nlm.nih.gov/pubmed/37293090
http://dx.doi.org/10.1101/2023.05.17.540386
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author Hammarlund, Jan A
Li, Shi-Yang
Wu, Gang
Lian, Jia-wen
Howell, Sacha J
Clarke, Rob
Adamson, Antony
Gonçalves, Cátia F.
Hogenesch, John B
Meng, Qing-Jun
Anafi, Ron C
author_facet Hammarlund, Jan A
Li, Shi-Yang
Wu, Gang
Lian, Jia-wen
Howell, Sacha J
Clarke, Rob
Adamson, Antony
Gonçalves, Cátia F.
Hogenesch, John B
Meng, Qing-Jun
Anafi, Ron C
author_sort Hammarlund, Jan A
collection PubMed
description Studies in shift workers and model organisms link circadian disruption to breast cancer. However, molecular rhythms in non-cancerous and cancerous human breast tissues are largely unknown. We reconstructed rhythms informatically, integrating locally collected, time-stamped biopsies with public datasets. For non-cancerous tissue, the inferred order of core-circadian genes matches established physiology. Inflammatory, epithelial-mesenchymal transition (EMT), and estrogen responsiveness pathways show circadian modulation. Among tumors, clock correlation analysis demonstrates subtype-specific changes in circadian organization. Luminal A organoids and informatic ordering of Luminal A samples exhibit continued, albeit disrupted rhythms. However, CYCLOPS magnitude, a measure of global rhythm strength, varied widely among Luminal A samples. Cycling of EMT pathway genes was markedly increased in high-magnitude Luminal A tumors. Patients with high-magnitude tumors had reduced 5-year survival. Correspondingly, 3D Luminal A cultures show reduced invasion following molecular clock disruption. This study links subtype-specific circadian disruption in breast cancer to EMT, metastatic potential, and prognosis.
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spelling pubmed-102456422023-06-08 Subtype-specific circadian clock dysregulation modulates breast cancer biology, invasiveness, and prognosis Hammarlund, Jan A Li, Shi-Yang Wu, Gang Lian, Jia-wen Howell, Sacha J Clarke, Rob Adamson, Antony Gonçalves, Cátia F. Hogenesch, John B Meng, Qing-Jun Anafi, Ron C bioRxiv Article Studies in shift workers and model organisms link circadian disruption to breast cancer. However, molecular rhythms in non-cancerous and cancerous human breast tissues are largely unknown. We reconstructed rhythms informatically, integrating locally collected, time-stamped biopsies with public datasets. For non-cancerous tissue, the inferred order of core-circadian genes matches established physiology. Inflammatory, epithelial-mesenchymal transition (EMT), and estrogen responsiveness pathways show circadian modulation. Among tumors, clock correlation analysis demonstrates subtype-specific changes in circadian organization. Luminal A organoids and informatic ordering of Luminal A samples exhibit continued, albeit disrupted rhythms. However, CYCLOPS magnitude, a measure of global rhythm strength, varied widely among Luminal A samples. Cycling of EMT pathway genes was markedly increased in high-magnitude Luminal A tumors. Patients with high-magnitude tumors had reduced 5-year survival. Correspondingly, 3D Luminal A cultures show reduced invasion following molecular clock disruption. This study links subtype-specific circadian disruption in breast cancer to EMT, metastatic potential, and prognosis. Cold Spring Harbor Laboratory 2023-05-19 /pmc/articles/PMC10245642/ /pubmed/37293090 http://dx.doi.org/10.1101/2023.05.17.540386 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Hammarlund, Jan A
Li, Shi-Yang
Wu, Gang
Lian, Jia-wen
Howell, Sacha J
Clarke, Rob
Adamson, Antony
Gonçalves, Cátia F.
Hogenesch, John B
Meng, Qing-Jun
Anafi, Ron C
Subtype-specific circadian clock dysregulation modulates breast cancer biology, invasiveness, and prognosis
title Subtype-specific circadian clock dysregulation modulates breast cancer biology, invasiveness, and prognosis
title_full Subtype-specific circadian clock dysregulation modulates breast cancer biology, invasiveness, and prognosis
title_fullStr Subtype-specific circadian clock dysregulation modulates breast cancer biology, invasiveness, and prognosis
title_full_unstemmed Subtype-specific circadian clock dysregulation modulates breast cancer biology, invasiveness, and prognosis
title_short Subtype-specific circadian clock dysregulation modulates breast cancer biology, invasiveness, and prognosis
title_sort subtype-specific circadian clock dysregulation modulates breast cancer biology, invasiveness, and prognosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245642/
https://www.ncbi.nlm.nih.gov/pubmed/37293090
http://dx.doi.org/10.1101/2023.05.17.540386
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