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  • The Pace Lab

The Pace Lab

picture of Betty S. Pace, MD

Betty S. Pace, MD

Professor Emeritus
Department of Pediatrics
Member, Tumor Signaling and Angiogenesis Program
Georgia Cancer Center
Medical College of Georgia
Augusta University 

 

Jump to: Research SummaryImpact on Georgia patientsResearch FocusPublicationsTeam

Contact Us

The Betty Pace Lab

 Health Sciences Campus

GCC - M. Bert Storey Research Building

1410 Laney Walker Blvd., CN-4116

(706) 721-3626

(706) 721-6895 (lab)

bpace@augusta.edu

Faculty Profile

Research Summary

Over the last three decades, the research focus in the Pace laboratory has been erythroid development as it relates to globin gene regulation and hemoglobin synthesis. As an NIH-funded physician-scientist, in the mid-1990s Dr. Pace pioneered in vivo drug treatment in the µLCRAγ transgenic mouse and later the human β-YAC mouse model. We were the first to demonstrate the ability to induce γ-globin expression using butyrate and 5-azacytidine in β-YAC mice; this model was later used to discover novel short-chain fatty acid derivatives that induce γ-globin. The 5-azacytidie analog, Decitabine, is currently in clinical testing as a novel fetal hemoglobin inducer. A second drug, Benserazide, which is an L-Dopa inhibitor, was shown to induce fetal hemoglobin, and a phase 1 clinical trial is underway in thalassemia patients. More recent work in the lab has focused on a genetic element, the Fetal Chromatin Domain, that is involved in the regulation of gamma globin gene expression during erythropoiesis. This element is a target for gene therapy development of novel treatments for sickle cell disease and thalassemia. 

Map of Georgia, USA, that shows counties and routes. A red push pin is pushed into Augusta, Georgia.

Impact on Patients in Georgia

Dr. Pace has spent three decades working toward better treatments for sickle cell disease—one of the most common serious genetic disorders in Georgia, where the disease burden is among the highest in the nation due to the state's large African American population.

Her foundational discoveries showing that fetal hemoglobin protects individuals with sickle cell disease from the worst effects of the disease, have directly led to clinical trials of two drugs now being tested in patients, including one already in Phase 1 trials for thalassemia.

For generations of Georgian families living with this painful, life-shortening condition, Dr. Pace's science represents a direct pathway from laboratory to relief.

Research Focus

  • Globin Gene Regulation
  • Erythropoiesis and development of drug therapy for sickle cell disease
  • Epigenetic modifications of chromatin structure
  • non-malignant hematology (sickle cell disease and thalassemia)
  • Histone hyperacetylation during development

Recent Publications

An intergenic silencer region regulates HBG expression.
Zhu X, Liu L, Takezaki M, Li Y, Bleoris L, Pace, BS. Blood RCI. 2026;2;2. https://doi.org/10.1016/j.brci.2026.100046 

IFN-g/JAK/STAT Axis Awakens the Delta Force of Hemoglobin.
Pace BS, Zhu X. Blood, 2026 Mar 5;147(10):1014-1015. 

Transsulfuration pathway activation attenuates oxidative stress and ferroptosis in sickle primary erythroblasts and transgenic mice. 
Xi C, Pang J, Xue W, Cui Y, Jiang N, Zhi W, Shi H, Horuzsko A, Pace BS, Zhu X. Commun Biol. 2025 Jan 6;8(1):15. doi: 10.1038/s42003-024-07424-7.PMID: 39762627 

Hematopoietic Cell Transplant compared with Standard Care in Adolescents and Young Adults with Sickle Cell Disease.
Walters MC, Eapen M, Liu Y, El Rassi F, Waller EK, Levine JE, Strouse JJ, Antin JH, Parikh SH, Bakshi N, Dampier CD, Jaroscak JJ, Bergmann S, Wong TE, Kota VK, Pace BS, Lekakis LJ, Lulla PD, Nickel R, Kasow KA, Popat UR, Smith WR, Yu LC, DiFronzo NL, Geller NL, Kamani N, Klings ES, Hassell K, Mendizabal AM, Sullivan K, Neuberg DS, Krishnamurti L. Blood Adv. 2024 Oct 29:bloodadvances.2024013926. doi: 10.1182/bloodadvances.2024013926. Online ahead of print. PMID: 39471440 

Endothelial ENaC-α Restrains Oxidative Stress in Lung Capillaries in Murine Pneumococcal Pneumonia-associated Acute Lung Injury.
Romero MJ, Yue Q, Ahn WM, Hamacher J, Zaidi Y, Haigh S, Sridhar S, Gonzales J, Hudel M, Huo Y, Verin AD, Pace BS, Stansfield BK, Maishan M, Neptune ER, Enkhbaatar P, Su Y, Chakraborty T, Gonsalvez G, Hummler E, Davis WB, Bogdanov VY, Fulton DJR, Csanyi G, Matthay MA, Eaton DC, Lucas R. Am J Respir Cell Mol Biol. 2024 Oct 15. doi: 10.1165/rcmb.2023-0440OC. Online ahead of print. PMID: 39405473 

Assessing Patterns of Telehealth Use Among People with Sickle Cell Disease Enrolled in Medicaid During the Start of the COVID-19 Pandemic.
Reeves SL, Plegue M, Patel PN, Paulukonis ST, Horiuchi SS, Zhou M, Attell BK, Pace BS, Snyder AB, Plaxco AP, Mukhopadhyay A, Smeltzer MP, Ellimoottil CS, Hulihan M. Telemed J E Health. 2024 Jun;30(7):e1971-e1979. doi: 10.1089/tmj.2023.0422. Epub 2024 Apr 11.PMID: 38603584 

Simvastatin-Mediated Nrf2 Activation Induces Fetal Hemoglobin and Antioxidant Enzyme Expression to Ameliorate the Phenotype of Sickle Cell Disease.
Xi C, Palani C, Takezaki M, Shi H, Horuzsko A, Pace BS, Zhu X. Antioxidants (Basel). 2024 Mar 11;13(3):337. doi: 10.3390/antiox13030337.PMID: 38539870 

Author Correction: Machine learning-based approaches for identifying human blood cells harboring CRISPR-mediated fetal chromatin domain ablations.
Li Y, Zaheri S, Nguyen K, Liu L, Hassanipour F, Pace BS, Bleris L. Sci Rep. 2024 Feb 12;14(1):3573. doi: 10.1038/s41598-024-54011-1. PMID: 38347089 

Characteristics of Emergency Department Visits Made by Individuals With Sickle Cell Disease in the U.S., 1999-2020.
Attell BK, Barrett PM, Pace BS, McLemore ML, McGee BT, Oshe R, DiGirolamo AM, Cohen LL, Snyder AB. AJPM Focus. 2023 Oct 30;3(1):100158. doi: 10.1016/j.focus.2023.100158. eCollection 2024 Feb. PMID: 38149076 

Bach1 inhibitor HPP-D mediates γ-globin gene activation in sickle erythroid progenitors.
Palani CD, Zhu X, Alagar M, Attucks OC, Pace BS. Blood Cells Mol Dis. 2024 Jan;104:102792. doi: 10.1016/j.bcmd.2023.102792. Epub 2023 Aug 17. PMID: 37633023 

Peer mentoring to support career advancement among underrepresented minority faculty in the programs to increase diversity among individuals engaged in health-related research (PRIDE).
Coleman TM, Starlard-Davenport A, Onwuemene OA, Stepleman LM, Pace BS. J Clin Transl Sci. 2023 Apr 24;7(1):e107. doi: 10.1017/cts.2023.535. eCollection 2023. PMID: 37313375 

Nrf2 sensitizes ferroptosis through l-2-hydroxyglutarate-mediated chromatin modifications in sickle cell disease.
Xi C, Pang J, Zhi W, Chang CS, Siddaramappa U, Shi H, Horuzsko A, Pace BS, Zhu X. Blood. 2023 Jul 27;142(4):382-396. doi: 10.1182/blood.2022018159.PMID: 37267508 Free PMC article. 

Research Team

photo of Mayuko Takezaki, MS

Mayuko Takezaki, MS

  • Lab Manager
  • PRIDE Program Research Coordinator

mtakezaki@augusta.edu

photo of Natasha Alford, MBA

Natasha Alford, MBA

  • Administrator

706-721-7607

nalford@augusta.edu

Reduce the Burden

The Georgia Cancer Center at Augusta University is dedicated to reducing the burden of cancer in Georgia and across the globe through superior care, innovation, and education. Through unprecedented expansion, the Georgia Cancer Center is providing access to more first-in-the-nation clinical trials, world-renowned experts and life-saving options.

Education & Research

M. Bert Storey Research
706-721-0570
cancer@augusta.edu

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706-721-6744
https://www.wellstar.org/

 

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