Andrew S. Goldstein, Ph.D.
Affiliations: | 2011 | University of California, Los Angeles, Los Angeles, CA |
Area:
Molecular Biology, Cell Biology, OncologyGoogle:
"Andrew Goldstein"Parents
Sign in to add mentor| Owen N. Witte | grad student | 2011 | UCLA | |
| (A role for stem/progenitor cells in the initiation of epithelial cancers.) | ||||
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Publications
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| Giafaglione JM, Crowell PD, Delcourt AML, et al. (2023) Prostate lineage-specific metabolism governs luminal differentiation and response to antiandrogen treatment. Nature Cell Biology |
| Wang CW, Clémot M, Hashimoto T, et al. (2023) A conserved mechanism for JNK-mediated loss of Notch function in advanced prostate cancer. Science Signaling. 16: eabo5213 |
| Crowell PD, Giafaglione JM, Jones AE, et al. (2023) MYC is a regulator of androgen receptor inhibition-induced metabolic requirements in prostate cancer. Cell Reports. 42: 113221 |
| Bernard MJ, Smith CM, Goldstein AS. (2023) Prostatic proliferative inflammatory atrophy: welcome to the club. The Journal of Pathology |
| Fox JJ, Hashimoto T, Navarro HI, et al. (2023) Highly multiplexed immune profiling throughout adulthood reveals kinetics of lymphocyte infiltration in the aging mouse prostate. Aging. 15 |
| Payne MC, Ho S, Hashimoto T, et al. (2023) Microwell-based flow culture increases viability and restores drug response in prostate cancer spheroids. Biotechnology Journal. e2200434 |
| Freeland J, Crowell PD, Giafaglione JM, et al. (2021) Aging of the progenitor cells that initiate prostate cancer. Cancer Letters. 515: 28-35 |
| Crowell PD, Giafaglione JM, Hashimoto T, et al. (2020) Distinct cell-types in the prostate share an aging signature suggestive of metabolic reprogramming. American Journal of Clinical and Experimental Urology. 8: 140-151 |
| Crowell PD, Giafaglione JM, Hashimoto T, et al. (2019) Evaluating the Differentiation Capacity of Mouse Prostate Epithelial Cells Using Organoid Culture. Journal of Visualized Experiments : Jove |
| Li Y, He Y, Butler W, et al. (2019) Targeting cellular heterogeneity with CXCR2 blockade for the treatment of therapy-resistant prostate cancer. Science Translational Medicine. 11 |