Targeting epigenetics: new insights into oral cancer progression and treatment
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Targeting epigenetics: new insights into oral cancer progression and treatment

08.05.2025 TranSpread

Oral squamous cell carcinoma (OSCC) is a leading cause of cancer-related deaths, and early detection is key to improving patient outcomes. However, the mechanisms driving the transition from preneoplastic lesions to full-blown cancer are not well understood. Previous research has primarily targeted advanced OSCC, overlooking the early stages of tumor progression. The new study focuses on lysine-specific demethylase 1 (LSD1), an epigenetic regulator that plays a significant role in OSCC development. By unraveling the molecular pathways through which LSD1 influences the tumor microenvironment, the study offers crucial insights into early-stage cancer biology and paves the way for innovative treatment strategies targeting this epigenetic modifier.

A study (DOI: 10.1038/s41368-025-00363-x) published in International Journal of Oral Science (2025) on April 17, 2025, uncovers the pivotal role of LSD1 in the progression of oral cancer. The multidisciplinary research from Manish Bais's laboratory at Boston University and the University of Florida, Drs. Sahay and Takada,, found that inhibiting LSD1, either through genetic modifications or the pharmacological agent SP2509, reversed OSCC preneoplasia and enhanced immune cell infiltration. These findings not only deepen our understanding of OSCC biology but also suggest that LSD1 inhibition could serve as a promising therapeutic strategy to prevent the progression of OSCC from preneoplastic stages, potentially transforming early-stage oral cancer treatment.

The study demonstrates that LSD1, an epigenetic regulator, plays a central role in the development of OSCC by controlling critical signaling pathways such as STAT3 and CDK7. The research team employed both genetic knockout models and pharmacological agents like SP2509 to inhibit LSD1 activity, revealing that this intervention effectively reversed the progression of OSCC preneoplasia in murine and feline models. Key observations included a reduction in tumor growth, the restoration of immune function through enhanced CD8+ T cell infiltration, and decreased levels of the immunosuppressive CTLA4 protein. In a novel veterinary clinical trial, the researchers found that Seclidemstat, a clinical candidate for LSD1 inhibition, was both safe and effective in inhibiting STAT3 signaling, further validating the translational potential of LSD1-targeted therapies. This study's findings underscore the importance of epigenetic regulation in OSCC progression and highlight the therapeutic potential of LSD1 inhibitors in preventing the transition from preneoplastic lesions to malignant tumors.

"Understanding how epigenetic regulators like LSD1 drive the progression of oral cancer which has been evaluated over several years in our lab, offers us new opportunities to intervene at a much earlier stage," said Dr. Manish Bais, lead senior author of the study. "Our findings demonstrate that targeting LSD1 not only halts tumor growth but also restores critical immune responses that can enhance anti-tumor immunity against cancer.. These results open up exciting possibilities for treating preneoplasia before it becomes OSCC and could ultimately improve patient survival rates."

The implications of this study are far-reaching, as inhibiting LSD1 could offer a new avenue for the treatment of OSCC. By targeting the early stages of tumor progression, LSD1 inhibitors, such as Seclidemstat, could provide a means to prevent OSCC before it becomes invasive, offering a significant breakthrough in early-stage cancer management. Additionally, the study suggests that combining LSD1 inhibition with existing immunotherapies could enhance immune responses and overcome tumor-induced immunosuppression. As clinical trials continue to investigate these therapies, LSD1 inhibition has the potential to reshape the treatment landscape for OSCC and other cancers driven by similar epigenetic mechanisms.

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References

DOI

10.1038/s41368-025-00363-x

Original Source URL

https://doi.org/10.1038/s41368-025-00363-x

Funding Information

The authors acknowledge NIH/NIDCR grant R01 DE031413 and CTSA pilot grant UL1TR001430 to Manish V. Bais.

About International Journal of Oral Science

International Journal of Oral Science (ISSN 1674-2818) was founded in 2009 and aims to publish all aspects of oral science and interdisciplinary fields, including fundamental, applied and clinical research. Covered areas include oral microbiology, oral and maxillofacial oncology, cariology, oral inflammation and infection, dental stem cells and regenerative medicine, craniofacial surgery, dental materials, oral biomechanics, oral, dental and maxillofacial genetic and developmental diseases.

Paper title: Lysine-specific demethylase 1 controls key OSCC preneoplasia inducer STAT3 through CDK7 phosphorylation during oncogenic progression and immunosuppression
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  • The potential mechanism after blocking LSD1 inhibits novel CDK7 phospho-protein networks and STAT3 signaling ultimately promotes CD8+ T cell infiltration and activation by relieving CTLA4-mediated immunosuppression
08.05.2025 TranSpread
Regions: North America, United States
Keywords: Science, Life Sciences

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