Academic Title:
Associate Professor
Primary Appointment:
Biochemistry and Molecular Biology
Additional Title:
Associate Professor
Email:
Location:
Bressler Research Building, Rm. 8041
Phone (Primary):
410-706-2192
Education and Training
2006 Ph.D., Biochemistry, Toronto University
2010 Postdoctoral Fellow, Sanford-Burnham Medical Research Institute
2013 Staff Scientist, Sanford-Burnham Medical Research Institute
Biosketch
My research interests aim to understand the molecular mechanisms governing prostate cancer progression and therapeutic resistance. My background is in prostate cancer biology, ubiquitination, epigenetics and transcriptional gene regulation.The experimental approaches used in my laboratory include molecular cell biology, biochemistry, transgenic mouse prostate cancer models (PTEN or Hi-Myc), and various genome-wide approaches (e.g. RNA-seq, ChIP-seq, ATAC-seq PRO-seq, Hi-ChIP, et al). We have also established stable collaboration with the experts in prostate cancer pathology or systems biology. Our studies reveal key roles for histone demethylase, ubiquitin ligases and oncogenic transcription factors in prostate cancer progression, and further understanding their mechanisms is critical towards identifying new targets and developing new rationale therapies for the advanced prostate cancer.
Research/Clinical Keywords
transcriptional gene regulation, epigenetics, signaling transduction, histone demethylase, ubiquitin ligase, androgen receptor, c-Myc, prostate cancer, castration-resistant prostate cancer, DNA damage response
Highlighted Publications
Jeon HY, Pornour M, Ryu H, Khadka S, Xu R, Jang J, Li D, Chen H, Hussain A, Fazli L, Gleave M, Dong X, Huang F, Wang Q, Barbieri C, Qi J. (2023). SMAD3 promotes expression and activity of the androgen receptor in prostate cancer. Nucleic Acids Research. 51, 2655-2670.
Xu S, Fan L, Jeon HY, Zhang F, Cui X, Mickle M, Peng G, Hussain A, Fazli L, Gleave M, Dong X, Qi J. (2020). p300-mediated acetylation of histone demethylase JMJD1A prevents its degradation by ubiquitin ligase STUB1 and enhances its activity in prostate cancer. Cancer Research. 80, 3074-3087.
Fan L, Zhang F, Xu S, Cui X, Hussain A, Fazli L, Gleave M, Dong X, Qi J. (2018). Histone demethylase JMJD1A promotes alternative splicing of AR variant 7 (AR-V7) in prostate cancer cells. PNAS. 115, E4584-93.
Fan L, Peng G, Sahgal N, Ladan F, Gleave M, Zhang Y, Hussain A, and Qi J. (2016). Regulation of c-Myc expression by the histone demethylase JMJD1A is essential for prostate cancer cell growth and survival. Oncogene. 35, 2441-2452.
Qi J, Tripathi M, Mishra R, Sahgal N, Fazil L, Ettinger S, Placzek WJ, Claps G, Chung LW, Bowtell D, Gleave M, Bhowmick N, and Ronai Z. (2013). The E3 ubiquitin ligase Siah2 contributes to castration-resistant prostate cancers by regulation of androgen receptor activity. Cancer Cell. 23, 332-346
Qi J, Nakayama K, Cardiff RD, Borowsky AD, Williams R, Krajewski S, Carpenter P, Mercola D, Bowtell D, and Ronai Z. (2010). Concerted activity of HIF and FoxA2 regulates formation of neuroendocrine prostate tumors and neuroendocrine phenotype of human metastatic prostate cancers. Cancer Cell 18, 23-38.