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The University of Southampton

Professor Graham Packham BSc (Hons), PhD

Professor of Molecular Oncology

Professor Graham Packham's photo

Professor Graham Packham is Professor of Molecular Oncology within Medicine at the University of Southampton.

Graham Packham has a first class honours degree in Biochemistry from the University of Leeds. He was awarded his PhD in 1992 from the University of London, following studies on regulation of Epstein-Barr virus gene expression at the Ludwig Institute for Cancer Research at St Mary’s Hospital, London. Professor Packham carried out his postdoctoral research at St Jude Children’s Research Hospital in Memphis, USA, where he was the recipient of the Martin Morrison Fellowship, investigating mechanisms of action of the c-Myc oncoprotein in the laboratory of Dr John Cleveland. He returned to the Ludwig Institute for Cancer Research in 1995 to establish an independent research group studying the molecular regulation of apoptotic in cancer cells. Professor Packham joined the Cancer Sciences Division of the University of Southampton as a Senior Lecturer in 2000 and was appointed Professor of Molecular Oncology in 2006.

Professor Packham leads a research group investigating molecular mechanisms controlling proliferation and survival in malignant lymphocytes and developing novel chemical compounds to interfere with key cancer promoting pathways.  He has published more than 130 peer-reviewed papers and patents. Graham Packham is also a cofounder of Karus Therapeutics , a University spin-out company involved in the development of novel therapeutics for cancer and inflammatory disease.


BSc (Hons), Biochemistry, University of Leeds (1988)
PhD, University of London (1992)

Appointments held

Reader , University of Southampton April 2004- August 2006

Senior Lecturer , University of Southampton January 2000 - March 2004

Assistant Member, Ludwig Institute for Cancer Research , London May 1995 - December 1999

Postdoctoral Fellow , St Jude Children's Research Hospital, Memphis, USA August 1992 - April 1995

Research interests

The research group has two major long-term interests
  • The molecular mechanisms controlling proliferation and survival in malignant lymphocytes
  • The development of novel chemical compounds to interfere with cancer promoting pathways

The goal of our work is to exploit our findings in the biology of cancer cells and the characterization of small molecule inhibitors, to develop novel treatments for cancer.

Molecular mechanisms controlling proliferation and survival in malignant lymphocytes

Our on-going research in this area is focused on chronic lymphocytic leukaemia (CLL), a disease of malignant B cells and the most common leukaemia in the Western world. The clinical course of CLL is highly heterogeneous with some patients having an indolent disease and others a rapidly progressing disease. Improved understand of the underlying biology mechanisms that cause this clinical heterogeneity is likely to lead to novel therapeutic approaches, especially for patients with the progressive disease subtype.

Our research is targeted at understanding signalling via the B-cell receptor and the microenvironment in CLL. In vitro analysis of signalling has demonstrated that individual CLL samples differ in their ability to transmit signals via the cell surface B-cell receptor. Retained signalling is associated with the presence of poor prognostic markers and a poor clinical outcome. Thus, antigen signalling via the B-cell receptor, in the context of specific tissue microenvironments, is considered to play a key role in driving cell proliferation and survival, leading to disease progression. Our current research aims to identify determinants of the differential responsiveness of CLL cells and the biological consequences of signalling via the B-cell receptor in this disease. Key research questions include;

  • How does “positive” signalling via the B-cell receptor drive malignant cell survival and proliferation in CLL?
  • How does the balance between BCR-driven “positive” signalling and anergy influence disease behaviour?
  • What are the functional and clinical significance of altered N-linked glycosylation sites of the BCR in malignant B cells?
  • How can we best select patients for treatment with novel inhibitors targeted towards BCR-associated signalling kinases?
Novel chemical compounds to interfere with cancer promoting pathways

Small chemical agonists and antagonists are key experimental tools and offer opportunities for drug discovery. Our laboratory has a long term track record in the biological characterisation of novel chemical compounds.

A major area of interest is the biological characterisation of chemical modulators of chromatin. Histone proteins are subject to a diverse array of post-translational modifications and alterations in these modifications can contribute to a range of diseases, including cancer and inflammatory conditions. We have performed extensive characterization of natural product histone deacetylase inhibitors, including spiruchostatin A, FK228 and azumamides. Our studies on bicyclic depsipeptide histone deacetylase inhibitors led to the creation of Karus Therapeutics, a University of Southampton spin-out company developing novel therapeutics for the treatment of cancer and inflammatory disease. We continue to characterize novel histone deacetylase inhibitors and to study chemical modulation of other chromatin modifying enzymes, including histone lysine methyltransferases and demethylases. A recent target for study is the histone methyltransferase EZH2 which is activated by mutation in follicular lymphoma. In collaboration with Professor Jude Fitzgibbon (Bart’s, London), we are evaluating the responses of primary lymphoma cells to new EZH2 inhibitors, as part of a programme to develop new personalised therapy approaches in this malignancy.

Research group

Cancer Sciences

Affiliate research group

Cancer Sciences Research group

Research project(s)

Application of novel acoustic trapping perfusion bioreactor to generate 3-D co-culture system for modelling tumour microenvironment interactions

Professor Graham Packham
Somers Cancer Research Building (MP 824) Southampton General Hospital Tremona Road Southampton SO16 6YD

Room Number : SGH/CSB/MP824

Facsimile: (023) 8120 5152

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