About me

Dr. Salma Mahmoud is a molecular biologist specializing in chromatin dynamics and epigenetics, focusing on how chromatin remodeling and epigenetic alterations regulate gene expression and drive disease. She earned her PhD at the University of Dundee, where she characterized the chromatin remodeling enzyme Fun30 and revealed its role in DNA replication and repair.

Her multidisciplinary research integrates genomics, molecular biology, and bioinformatics to investigate epigenetic mechanisms in cancer, cardiomyopathies, infectious, and neurodevelopmental disorders. Dr. Mahmoud’s key contributions include redefining RUNX3 as an oncogenic chromatin regulator in gastric cancer, identifying novel ubiquitin inhibitors with therapeutic potential, and uncovering chromatin-mediated mechanisms in cardiac and infertility disorders.

She currently leads a project on the epigenetic and therapeutic potential of African medicinal plants and serves as an International Ambassador of the Biochemical Society (UK). At UM6P, Dr. Mahmoud aims to establish the Chromatin Dynamics and Epigenetic Research Program (CDERP) to bridge fundamental chromatin biology with translational medicine and advance precision health innovations across Africa.

Dr. Salma Mahmoud is a visionary epigenetic scientist whose pioneering research has transformed our understanding of chromatin remodeling and its profound influence on gene regulation, disease, and human health. Holding a PhD from the University of Dundee’s Wellcome Trust Centre for Gene Regulation and Expression, she has dedicated her career to unraveling the molecular mechanisms that govern chromatin dynamics and epigenetic regulation.

Dr. Mahmoud’s groundbreaking work has earned her over 26 influential publications and 1,399+ citations, establishing her as an emerging leader in the global scientific community. Her research spans the epigenomics of cancer, cardiovascular disease, cardiomyopathy, and developmental disorders, where she has made pivotal discoveries such as redefining RUNX3 as a novel chromatin regulator in gastric cancer — a paradigm-shifting finding that challenges long-held views of RUNX3 as merely a tumor suppressor and opens the door to new therapeutic strategies.

Her doctoral research characterized Fun30, an ATP-dependent chromatin remodeling enzyme, as a homodimeric factor that mediates nucleosome remodeling through histone dimer exchange — uncovering key insights into DNA replication and repair. Building on this foundation, Dr. Mahmoud has developed a multidisciplinary research portfolio integrating genomics, molecular biology, and bioinformatics to explore epigenetic mechanisms in disease and identify translational applications for precision medicine.

Among her most notable contributions are:

RUNX3 in Gastric Cancer: Identification of RUNX3 as an oncogenic chromatin regulator that alters heterochromatin architecture and drives tumorigenesis.

Targeting Ubiquitin Pathways: Discovery of three novel ubiquitin inhibitors, including one that selectively targets RUNX3 and induces autophagy-mediated cell death in metastatic gastric cancer.

Epigenetics of Cardiomyopathy: Demonstration of CaMKIIδB as a chromatin modifier linking calcium signaling to cardiac hypertrophy and identification of ATF2 ubiquitination with FBXO32 in stress-mediated dilated cardiomyopathy.

Neurodevelopment and Infertility: Discovery of PHC1’s role in DNA damage response in microcephaly and the impact of TLE6 phosphorylation in early female embryonic lethality.

At the University of Botswana, Dr. Mahmoud leads an innovative project on the Epigenetic Potential of Indigenous African Flora, exploring the molecular and therapeutic properties of African medicinal plants for anti-cancer, antimicrobial, and bioremediation applications. This aligns with Africa’s growing bio-innovation ecosystem and her broader commitment to using science as a tool for sustainable, culturally rooted innovation.

Dr. Mahmoud’s scientific influence extends beyond the laboratory. She is a global scholar and speaker, presenting her research at international conferences across Singapore, Saudi Arabia, the UAE, the USA, China, and even teaching at the American University of Afghanistan during the pandemic. She currently serves as an International Ambassador of the Biochemical Society (UK), where she advocates for global scientific collaboration and the empowerment of young researchers, particularly women in STEM.

Beyond her scientific pursuits, Dr. Mahmoud is deeply captivated by the intersection of epigenetics and the social sciences, exploring how societal and environmental forces shape the very genes that influence our health. Her curiosity extends into art, philosophy, and creative writing, where she applies epigenetic concepts to understand the creative process and the evolution of human thought. Her work thus bridges science, society, and creativity, illustrating how molecular mechanisms of life can also inspire reflection on culture, identity, and resilience.

icon-membership
Other Memberships/Affiliations
Biochemical Society

Degrees:

2011
Doctorate
Structural, Cell and Molecular Biology
2006
Master
Structural, Cell and Molecular Biology
2002
Undergraduate
Structural, Cell and Molecular Biology

Publications resulting from Research
Selected Highlighted Publications:

Scopus ID: 14036781300, h-index: 15
https://www.scopus.com/authid/detail.uri?authorId=14036781300

Google Scholar: https://scholar.google.com/citations?hl=en&user=SsVohokAAAAJ&view_op=list_works
• Citations as of 12th , Oct, 2025: 1394
• h-index: 18, i10-index:18
• OCRID ID: 0000-0003-1475-9483
• Japanese Researchmap Registration Number:1075

1. Nadya Alyacoub, Falah Almohanna, Alanoud Alqassem, Salma Awad Mahmoud, Amer Almzroua, Abdullah mohamed Assiri. Dcaf17 knockdown integrates mitochondrial-lysosomal dysfunction with ferroptosis, NLRP3 inflammasome signaling and necroptosis.bioRxiv. 2025. doi.org/10.1101/2025.06.04.657829
2. Salma Awad Mahmoud, Isabelle Bonne, Aik Yong Sim, Gehan Labib Abuelenain. Runx3 Acts as Homodimeric Chromatin Binding Factor Regulating Heterochromatin-Mediated Cancerous Phenotype. bioRxiv. 2024. doi.org/10.1101/2024.08.16.608297
3. Almurshidi BH, Fahmy Z, El-Shennawy A, Selim EAH, Hammam OA, Okasha H, Al-Hajj W, Mahmoud SA, Abuelenain GL. A multimodality therapeutic application on Toxoplasma gondii encephalitis utilizing Spiramycin and 'de novo' Ferula asafetida in immunodeficient mice. Parasite Immunol. 2023 Dec;45(12):e13014. doi: 10.1111/pim.13014.
4. S Mahmoud, GLA Elenain, N Al Yacoub, M Al Zaabi. T100 Expression profiling of epigenetics and chromatin remodeling factors in human heart failure: The road towards precision medicine. Clinica Chemica Acta. 2022. 530, S95. doi.org/10.1016/j.cca.2022.04.567
5. Nadya Al-Yacoub, Dilek Colak, Salma Awad Mahmoud, Maya Hammonds, Kunhi Muhammed, Olfat Al-Harazi, Abdullah M Assiri, Jehad Al-Buraiki, Waleed Al-Habeeb, Coralie Poizat. Mutation in FBXO32 causes dilated cardiomyopathy through up-regulation of ER-stress mediated apoptosis. Commun Biol. 2021 Jul 16;4(1):884. doi: 10.1038/s42003-021-02391-9.
6. Pharaon LF, El-Orabi NF, Kunhi M, Al Yacoub N, Awad SM, Poizat C. Rosiglitazone promotes cardiac hypertrophy and alters chromatin remodeling in isolated cardiomyocytes. Toxicol Lett. 2017 Oct 5;280:151-158. doi: 10.1016/j.toxlet.2017.08.011.
7. Al-Yacoub N, Shaheen R, Awad SM, Kunhi M, Dzimiri N, Nguyen HC, Xiong Y, Al-Buraiki J, Al-Habeeb W, Alkuraya FS, Poizat C. FBXO32, encoding a member of the SCF complex, is mutated in dilated cardiomyopathy.Genome Biol. 2016 Jan 11;17(1):2. doi: 10.1186/s13059-015-0861-4.
8. Awad S, Al-Haffar K, Marashly Q, Quijada P, Kunhi M, Al-Yacoub N, Wade FS, Mohammed SF, Al-Dayel F, Sutherland G, Assiri A, Sussman M, Bers D, Al-Habeeb W, Poizat C. Control of Histone H3 Phosphorylation by CaMKII in Response to Hemodynamic Cardiac Stress. J Pathol. 2014 Nov 25. doi: 10.1002/path.4489.
9. Alazami AM*, Awad SM *, Coskun S, Al-Hassan S, Hijazi H, Abdulwahab FM, Poizat C, Alkuraya FS. TLE6 mutation causes the earliest known human embryonic lethality. Genome Biol. 2015 Nov 5;16(1):240. * Equal contributing authors. doi: 10.1186/s13059-015-0792-0.
10. Mahmoud SA, Poizat C.Epigenetics and chromatin remodeling in adult cardiomyopathy. J Pathol. 2013 Oct; 231(2):147-57. doi: 10.1002/path.4234.
11. Awad S, Al-Dosari MS, Al-Yacoub N, Colak D, Salih MA, Alkuraya FS, Poizat C.Mutation in PHC1 implicates chromatin remodeling in primary microcephaly pathogenesis.Hum Mol Genet. 2013 Jun 1;22(11):2200-13. doi: 10.1093/hmg/ddt072.