Metabolic Dysregulation Controls Endocrine Therapy–Resistant Cancer Recurrence and Metastasis
Author(s) -
Malachi A. Blundon,
Subhamoy Dasgupta
Publication year - 2019
Publication title -
endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.674
H-Index - 257
eISSN - 1945-7170
pISSN - 0013-7227
DOI - 10.1210/en.2019-00097
Subject(s) - metastasis , endocrine system , crosstalk , cancer , transcription factor , biology , prostate cancer , bioinformatics , cancer research , nuclear receptor , tumor progression , medicine , endocrinology , gene , hormone , genetics , physics , optics
Cancer recurrence and metastasis involves many biological interactions, such as genetic, transcription, environmental, endocrine signaling, and metabolism. These interactions add a complex understanding of cancer recurrence and metastatic progression, delaying the advancement in therapeutic opportunities. We highlight the recent advances on the molecular complexities of endocrine-related cancers, focusing on breast and prostate cancer, and briefly review how endocrine signaling and metabolic programs can influence transcriptional complexes for metastasis competence. Nuclear receptors and transcriptional coregulators function as molecular nodes for the crosstalk between endocrine signaling and metabolism that alter downstream gene expression important for tumor progression and metastasis. This exciting regulatory axis may provide insights to the development of cancer therapeutics important for these desensitized endocrine-dependent cancers.
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