ETS Related Gene mediated Androgen Receptor Aggregation and Endoplasmic Reticulum Stress in Prostate Cancer Development
Abstract Mechanistic studies of deregulated ERG in prostate cancer and other cancers continue to enhance its role in cancer biology and its utility as a biomarker and therapeutic target. Here, we show that ERG, through its physical interaction with androgen receptor, induces AR aggregation and endop...
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2017
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oai:doaj.org-article:d5ee1bf16e654954959d31a94f341a872021-12-02T12:30:35ZETS Related Gene mediated Androgen Receptor Aggregation and Endoplasmic Reticulum Stress in Prostate Cancer Development10.1038/s41598-017-01187-42045-2322https://doaj.org/article/d5ee1bf16e654954959d31a94f341a872017-04-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-01187-4https://doaj.org/toc/2045-2322Abstract Mechanistic studies of deregulated ERG in prostate cancer and other cancers continue to enhance its role in cancer biology and its utility as a biomarker and therapeutic target. Here, we show that ERG, through its physical interaction with androgen receptor, induces AR aggregation and endoplasmic reticulum stress in the prostate glands of ERG transgenic mice. Histomorphological alterations and the expression of ER stress sensors Atf6, Ire1α, Perk, their downstream effectors Grp78/BiP and eIF2α in ERG transgenic mouse prostate glands indicate the presence of chronic ER stress. Transient activation of apoptotic cell death during early age correlated well with the differential regulation of ER stress sensors, in particular Perk. Epithelial cells derived from ERG transgenic mouse prostates have increased prostasphere formation with resistance to radiation induced cell death. Continued activation of cell survival factors, Atf6 and Ire1α during chronic ER stress due to presence of ERG in prostate epithelium induces survival pathways and provides a selection pressure in the continuum of ERG dependent neoplastic process. These novel insights will enhance the understanding of the mechanistic functions of ERG in prostate tumor biology and towards development of early targeted therapeutic strategies for prostate cancer.Taduru L. SreenathShiela S. MacalindongNatallia MikhalkevichShashwat SharadAhmed MohamedDenise YoungTalaibek BorbievCharles XavierRishita GuptaMuhammad JamalKevin BabcockShyh-Han TanMarja T. NevalainenAlbert DobiGyorgy PetrovicsIsabell A. SesterhennInger L. RosnerCharles J. BieberichPeter NelsonValeri VasioukhinShiv SrivastavaNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-16 (2017) |
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Medicine R Science Q Taduru L. Sreenath Shiela S. Macalindong Natallia Mikhalkevich Shashwat Sharad Ahmed Mohamed Denise Young Talaibek Borbiev Charles Xavier Rishita Gupta Muhammad Jamal Kevin Babcock Shyh-Han Tan Marja T. Nevalainen Albert Dobi Gyorgy Petrovics Isabell A. Sesterhenn Inger L. Rosner Charles J. Bieberich Peter Nelson Valeri Vasioukhin Shiv Srivastava ETS Related Gene mediated Androgen Receptor Aggregation and Endoplasmic Reticulum Stress in Prostate Cancer Development |
| description |
Abstract Mechanistic studies of deregulated ERG in prostate cancer and other cancers continue to enhance its role in cancer biology and its utility as a biomarker and therapeutic target. Here, we show that ERG, through its physical interaction with androgen receptor, induces AR aggregation and endoplasmic reticulum stress in the prostate glands of ERG transgenic mice. Histomorphological alterations and the expression of ER stress sensors Atf6, Ire1α, Perk, their downstream effectors Grp78/BiP and eIF2α in ERG transgenic mouse prostate glands indicate the presence of chronic ER stress. Transient activation of apoptotic cell death during early age correlated well with the differential regulation of ER stress sensors, in particular Perk. Epithelial cells derived from ERG transgenic mouse prostates have increased prostasphere formation with resistance to radiation induced cell death. Continued activation of cell survival factors, Atf6 and Ire1α during chronic ER stress due to presence of ERG in prostate epithelium induces survival pathways and provides a selection pressure in the continuum of ERG dependent neoplastic process. These novel insights will enhance the understanding of the mechanistic functions of ERG in prostate tumor biology and towards development of early targeted therapeutic strategies for prostate cancer. |
| format |
article |
| author |
Taduru L. Sreenath Shiela S. Macalindong Natallia Mikhalkevich Shashwat Sharad Ahmed Mohamed Denise Young Talaibek Borbiev Charles Xavier Rishita Gupta Muhammad Jamal Kevin Babcock Shyh-Han Tan Marja T. Nevalainen Albert Dobi Gyorgy Petrovics Isabell A. Sesterhenn Inger L. Rosner Charles J. Bieberich Peter Nelson Valeri Vasioukhin Shiv Srivastava |
| author_facet |
Taduru L. Sreenath Shiela S. Macalindong Natallia Mikhalkevich Shashwat Sharad Ahmed Mohamed Denise Young Talaibek Borbiev Charles Xavier Rishita Gupta Muhammad Jamal Kevin Babcock Shyh-Han Tan Marja T. Nevalainen Albert Dobi Gyorgy Petrovics Isabell A. Sesterhenn Inger L. Rosner Charles J. Bieberich Peter Nelson Valeri Vasioukhin Shiv Srivastava |
| author_sort |
Taduru L. Sreenath |
| title |
ETS Related Gene mediated Androgen Receptor Aggregation and Endoplasmic Reticulum Stress in Prostate Cancer Development |
| title_short |
ETS Related Gene mediated Androgen Receptor Aggregation and Endoplasmic Reticulum Stress in Prostate Cancer Development |
| title_full |
ETS Related Gene mediated Androgen Receptor Aggregation and Endoplasmic Reticulum Stress in Prostate Cancer Development |
| title_fullStr |
ETS Related Gene mediated Androgen Receptor Aggregation and Endoplasmic Reticulum Stress in Prostate Cancer Development |
| title_full_unstemmed |
ETS Related Gene mediated Androgen Receptor Aggregation and Endoplasmic Reticulum Stress in Prostate Cancer Development |
| title_sort |
ets related gene mediated androgen receptor aggregation and endoplasmic reticulum stress in prostate cancer development |
| publisher |
Nature Portfolio |
| publishDate |
2017 |
| url |
https://doaj.org/article/d5ee1bf16e654954959d31a94f341a87 |
| work_keys_str_mv |
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