Huidong Shi, PhDHuidong Shi, PhD

Professor, Biochemistry and Molecular Biology

Professor, Graduate Studies

Member, Molecular Oncology and Biomarkers Program 

Georgia Cancer Coalition Distinguished Scholar

Research Summary

Dr. Shi is interested in understanding the complex epigenetic regulation in normal and tumor cells. He has pioneered the development of high-throughput technologies for DNA methylation analysis. His laboratory utilized the next-generation sequencing-based approaches to generate the epigenomic profiles of chronic lymphocytic leukemia, breast cancer, and brain tumors. Presently, Dr. Shi is using single-cell genomics and epigenomics approaches in combination with statistical and bioinformatic tools to decipher transcriptional and epigenetic regulation in the engineered T cells for cancer immunotherapy and stromal cells in the tumor microenvironment.

Contact Us

The Huidong Shi Lab

Health Sciences Campus

Georgia Cancer Center - M. Bert Storey Research Building

1410 Laney Walker Blvd., CN-2138, Augusta, GA 30912

(706) 721-6000

Research Interests

Epigenomics of chronic lymphocytic leukemia

One of the primary focuses of our research is chronic lymphocytic leukemia (CLL), which is the most common form of adult leukemias in the United States. We are interested in understanding the molecular heterogeneity of CLL and identifying prognostic biomarkers and novel therapeutic targets in CLL. Using genome-wide DNA methylation profiling, we have shown that two molecular subtypes of CLL (IGHV mutated vs. unmutated CLL) have distinct DNA methylation profiles that seem to represent epigenetic imprints from normal B-cell subpopulations. Through integrated epigenomics and gene expression analyses, specific genes have been identified that distinguish new clinico-biological subtypes of CLL. We found that many hypomethylated genes in CLL are associated with super-enhancers and marked with substantial histone H3K27 acetylation enrichment. On-going studies are designed to further understand the function of these hypomethylated genes and target the super-enhancer-driven oncogene transcription using small molecule inhibitors. A vital feature of the clinical course of CLL is that patients with CLL also present with a humoral immune deficiency that worsens with disease progression. We are investigating the molecular mechanisms of T-cell dysfunction in CLL using epigenomic approaches.

Targeting spliceosome for cancer therapy

Splicing factor SF3B1 is frequently mutated in a spectrum of malignancies, from hematological (e.g., CLL) to solid tumors and has been suggested as a potential therapeutic target. We demonstrated that the SF3B1 modulator sudemycin D6 (SD6) effectively inhibits CLL cell growth and induces apoptosis in in-vitro and in-vivo models. Using RNA-seq analysis, we discovered that genes associated with SD6-induced splicing changes are significantly enriched in the B-cell receptor (BCR) and PI3K signaling pathways, including BLNK, BTK, AKT, PLCγ2, and PI3Kδ. SD6 also induced a time-dependent exon-skipping event in MCL-1 mRNA and resulted in significant downregulation of another anti-apoptotic gene TRAF1. We found that SD6 can synergize with the established CLL therapies ibrutinib, idelalisib, and venetoclax to induce apoptosis in primary CLL cells co-cultured with bone marrow stromal cells and T-cell-derived cytokines. We are currently collaborating with a pharmaceutic startup for future clinical development of spliceosome modulators and potential combination therapies to treat CLL.

Epigenetic regulation of IDO expression in triple negative breast cancer

Indoleamine 2,3-dioxygenase (IDO), a single chain oxidoreductase that serves as a catalyst for the degradation of tryptophan into kynurenine, has emerged as a critical player in T-cell suppression and the induction of immune tolerance to tumors. We discovered that promoter hypomethylation and up-regulation of IDO1, which encodes the IDO enzyme, is a unique molecular feature of TNBC or basal-like breast cancer compared to other subtypes of breast cancer. Our in vitro studies demonstrated that IDO1 promoter methylation controls its expression in response to the interferon γ treatment in breast cancer cells. This novel finding leads us to hypothesize that IDO1 promoter methylation may be developed into a biomarker for predicting TNBC prognosis and the response to IDO inhibitor-based immunotherapy. Currently, we are determining the prognostic value of IDO1 promoter methylation in TNBC patients and dissecting the mechanisms of epigenetic regulation of IDO1 expression in breast cancer cells. Besides, we have identified several small molecules that inhibit interferon γ-induced IDO1 expression at the transcription level. We are investigating the molecular mechanisms of these drugs and evaluating their ability to block IDO1 expression in breast cancer cells.

Research Team

photo of Lirong Pei

Lirong Pei

  • Research Associate


photo of Mercy Kehinde-Ige

Mercy Kehinde-Ige

  • PhD Student
photo of Apeksha Anand

Apeksha Anand

  • Postdoctoral Fellow


photo of Victor Enriquez Castro

Victor Enriquez Castro

  • Visiting Student Intern