For the first time, researchers at Boston University have shown that T-cell leukaemia cells use a particular cycle, called the TCA or Kreb cycle, to support their growth and survival.

The findings from Dr Hui Feng and her postdoctoral trainees (Dr Nicole M. Anderson, Dr Dun Li, and Dr Fabrice Laroche), which appear online in the journal Leukemia, may lead to the development of therapeutics to effectively kill these types of tumour cells by targeting a critical enzyme called DLST that exists in the TCA cycle.

Despite improvement of T-cell leukaemia treatment, this disease is fatal in more than 20 percent of children and 50 percent of adult cases.

Additionally, current treatment protocols are highly toxic.

Using an experimental model, BUSM researchers performed genetic screenings to identify mutations that can specifically suppress tumour development.

The screening led to the identification of the TCA cycle enzyme DLST as an important contributor to T-cell acute lymphoblastic leukaemia development.

Further analysis using human T-cell leukaemia cells demonstrated that inhibiting the DLST enzyme activity could effectively kill human T-cell leukaemia cells.

"Researchers have wrongly assumed that cancer cells do not use the TCA cycle to support their growth. Our new findings provide solid evidence that these cancer cells depend on the TCA cycle for their survival," explained corresponding author Hui Feng, MD, PhD, assistant professor of pharmacology and medicine at BUSM.

"Additionally we demonstrated the importance of DLST in T-cell leukaemia development, and have identified a targetable enzyme for T-cell leukaemia treatment," she added.

The researchers believe the therapeutic benefit of DLST inhibition may extend to cancers other than T-cell leukaemia.

Source: Boston University Medical Campus