A study of the androgen mediated transcriptome and AR interactome in AI resistant breast cancer
thesisposted on 27.01.2021, 09:49 authored by Rachel Bleach
Aromatase inhibitors (AI) are the vanguard treatment for hormone receptor positive, postmenopausal breast cancer, however, acquired resistance occurs in up to 40% of patients. AI therapies, by their mechanism of action, create a predominantly androgenic steroid environment. In this study, a multi-omic approach was undertaken to elucidate the role of the androgen receptor (AR) in AI resistant breast cancer. Evidence from this study suggests that cancer cells adapt to utilise the adrenal prohormone, androstenedione and/or its metabolites, to promote resistance and survival in AI resistance. AR protein levels are associated with better disease-free survival in a breast cancer tissue microarray (TMA), however, in an AI treated cohort this does not hold. This research has found AR
transcriptional activity, and serum levels of the steroid, androstenedione, to be elevated in patients who recur on AI therapy. RNA sequencing of AI resistant cells (LetR) identified an AR mediated gene signature arising from
the altered steroid environment associated with AI therapy resistance. This gene signature is associated with cells that have adapted to utilise androstenedione and/or its metabolites as demonstrated by transcriptional attenuation when cells are re-exposed to estradiol. LetR cell growth is AR dependent as a reduction in viability is observed with the anti-AR therapy enzalutamide. Furthermore, enzalutamide abrogates colony formation, mammosphere generation and the self-renewal capabilities of LetR cells,
which is not observed in sensitive cell counterparts. LC–MS/MS analysis identified androgen-mediated AR protein interactors unique to the AI resistant model. Further analysis of these identified a differential protein interaction network in AI resistant and sensitive cells. As breast cancer is a steroid sensitive disease, this study provides important insight into understanding the impact of alterations in the steroid microenvironment. Furthermore, the AR-mediated gene signature and AR protein partners identified in this study provide novel insight into the
dichotomous role of AR in breast cancer and could be used to better identify patients who could benefit from anti-AR therapy.
First SupervisorDr. Marie McIlroy
Second SupervisorProfessor Arnold Hill
CommentsA thesis submitted for the degree of Doctor of Philosophy from the Royal College of Surgeons in Ireland in 2020.
Published CitationBleach R. A study of the androgen mediated transcriptome and AR interactome in AI resistant breast cancer [PhD Thesis]. Dublin: Royal College of Surgeons in Ireland; 2020.
Degree NameDoctor of Philosophy (PhD)
Date of award31/05/2020
- Doctor of Philosophy (PhD)