Shou-Jiang (SJ) Gao, PhD

  • Professor

Education & Training

  • Postdoc, Columbia University, 1994-96
  • Postdoc, University of Massachusetts, Amherst, 1993-94
  • PhD in Microbiology, University of Bordeaux (France), 1993
  • BS in Agronomy, South China Agricultural University (China), 1984

Research Interest Summary

Molecular Basis of Cancer and Genetic Diseases, Host-Pathogen Interactions, Microbial and Viral Pathogenesis

Research Interests

Dr. Gao's Laboratory is at the forefront of investigating cancer viruses and their associated malignancies, with a primary focus on elucidating the mechanisms of oncogenesis induced by Kaposi's sarcoma-associated herpesvirus (KSHV) for nearly three decades. Our research endeavors have expanded to encompass a broad spectrum of viral pathogens, including human papillomavirus (HPV), SARS-CoV-2, and Zika virus.

Using a multidisciplinary approach, we establish numerous infection models of primary cells and employ reverse genetics to study various aspects of KSHV infection, including acute infection, viral latency and reactivation, virus-host interactions, cellular transformation, and tumorigenesis. Our comprehensive methodology integrates expertise in virology, molecular and cellular biology, biochemistry, genomics, computational biology, and clinical studies.

Through our investigations, we have uncovered the complex mechanisms by which KSHV subverts the host immune response, induces inflammation and angiogenesis, and reprograms metabolic pathways, the epigenome, and the epitranscriptome. These discoveries have led to the identification of viral and cellular essential genes critical to these processes and have facilitated the identification of novel therapeutic targets and agents.

Furthermore, our research has extended beyond cancer viruses to elucidate novel cellular functions, such as the recent discovery of the tumor suppressor role of a novel arginine sensor, CASTOR1, in KSHV-induced cancer, as well as its implications in breast and lung cancer. Leveraging genetic mouse models, we have demonstrated the crucial function of CASTOR1 in regulating innate and adaptive immunity, which plays an integral role in the interactions between cancer cells and the tumor microenvironment.

Overall, Dr. Gao's Laboratory is committed to advancing our understanding of cancer viruses and associated malignancies, with the ultimate goal of developing innovative strategies for prevention, diagnosis, and treatment. Our research contributes to the broader scientific community's efforts to combat these devastating diseases and improve patient outcomes.

Publications

Chen LP, Ding L, Wang X, Gao S-J. 2023. Activation of glucocorticoid receptor signaling inhibits KSHV-induced inflammation and tumorigenesis. mBio, 15, 1:e0301123. doi: 10.1101/2023.11.10.566578 | View abstract

Das A, Meng W, Li ZT, Hasib MM, Hugh G, da Silva SR, Chen LP, Sic GL, Paniz Monodolfi AE, BRyce C, Grimes Z, Sordillo EM, Cordeon-Cardo C, Rivera KP, Flores F, Chiu YC, Huang YF, Gao S-J. 2023. Cellular and immune signatures, and pathological trajectories of fatal COVID-19 lungs defined by in situ spatial single-cell transcriptome analysis. Journal of Medical Virology, 95, 8: e29009, doi: 10.1002/jmv.29009 | View abstract

Yan Q, Zhou J, Wang Z, Ding X, Ma X, Li W, Jia X, Gao S-J, Lu C. 2023. NATO10-dependent N4-acetylcytidine modification mediates PAN RNA stability, KSHV reactiviation, and IFI16 sensing and inflammasome activation. Nature Communication, 14, 1:6327 doi: 10.1038/s41467-023-42135-3 | View abstract

Shi J, Jia X, He Y, Ma X, Qi X, Li W, Gao S-J, Yan Q, Lu C. 2023.  Immune evasion strategy involving propionylation by the KSHV interferon regulatory factor 1 (vIRF1). PLoS Pathogens, 19, 4: e1011324 doi: 10.1371/journal.ppat.1011324 | View abstract

Feng J, Meng W, Zhang T, Chen LP, Zhang XQ, MArkazi A, Yuan WM, huang YF, Gao S-J. 2023. N6-methyladenosine and reader protein YTHDF2 enhance immune response by targeting DUSP1 mRNA degredation and activating mitogen-activated protein kinases during bacterial and viral infections. mBio, 14, 1: e0334922. doi: 10.1128/mbio.03349-22 | View abstract

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