A research team led by Hong Kong, S.A.R., China Baptist University (HKBU) has developed a novel anti-Epstein-Barr virus (EBV) drug that can selectively disrupt a viral protein produced by EBV, leading to the shrinkage of tumors caused by the virus. It is the first known agent to successfully target the virus and disturb its latency in tumor cells in this way.

The strategy of reactivation of EBV from its latency is a new trend in nasopharyngeal carcinoma (NPC) therapy, and some non-specific, anti-viral drugs have recently entered phase one or phase two clinical trials. Our new drug represents the first specific targeted agent to disrupt a single viral protein and to potently reactivate EBV from its latency. These research results were published in the international journal Proceedings of the National Academy of Sciences.

EBV is a human herpesvirus that spreads through close person to person contact. It has infected more than 90% of the human population worldwide.

The human immune system usually suppresses the EBV activity effectively, but in some people the virus continues to exist in the human body and becomes a risk factor for many cancers, such as post-transplant lymphoproliferative disease, Hodgkin lymphoma, Burkitt lymphoma, T/Natural Killer cell lymphomas, some gastric carcinoma, and NPC — a highly prevalent cancer in Hong Kong, S.A.R., China and southern China.

In search of new therapies for EBV-related carcinomas, a research team comprising Professor Gary Wong Ka-Leung, Head of the Department of Chemistry, HKBU; Professor Mak Nai Ki, Professor, Department of Biology, HKBU; Dr Lung Hong Lok, Assistant Professor, Department of Chemistry, HKBU; and Dr Jiang Lijun, Research Assistant Professor, Department of Applied Biology and Chemical Technology at The Hong Kong, S.A.R., China Polytechnic University, developed a novel drug which has shown promising results in an animal model.

EBNA1 is the viral protein which is expressed in all EBV-associated tumour cells. EBNA1 plays a vital role in the maintenance of the viral genome and the proliferation of EBV-infected tumor cells.

The research team constructed a new peptide drug with higher affinity to the EBNA1 protein, leading to the disruption of the structure and functions of EBNA1. The tumor cells will thus stop proliferating and die eventually.

Furthermore, the study also showed that the new drug emits unique responsive fluorescence signals once bound with EBNA1 or its metal cofactor. The imaging results demonstrated that the drug can enter the nucleus of EBV-infected cells, where EBNA1 resides, to inhibit their growth and division. It could also potentially be applied to tumor cell imaging in the human body.

After EBV infection, the virus can establish latent infection, remain hidden in the infected cells, and promote pathogenic development of the tumor cells. Disruption of EBV latent and induction of EBV lytic cycle is one of the current strategy to control of EBV-associated malignancy. As a result, the EBV-infected cells will die and will be eliminated by the immune system. The research team discovered that the new drug can reactivate EBV lytic cycle through the disruption of EBNA1, and provides a new mentality of treatment of NPC.