Experimental drug hits cancer stem cells
CHICAGO (Reuters) – An experimental drug was effective at killing breast cancer stem cells – a kind of master cancer cell that resists chemotherapy, US researchers said last week. Studies in animals and women with advanced breast cancer showed the experimental compound MK-0752, under development by Merck & Co. Inc., was able to kill off cancer stem cells that linger in the breast after chemotherapy.
Researchers are still trying to understand the role cancer stem cells play in promoting different types of cancer, but many teams think they may explain why so many cancers come back even after treatment with powerful chemotherapy and radiation.
"These cells are different from the tumour. They are resistant to therapy. They regrow. They cause relapse and metastases," said Dr. Jenny Chang of Baylor College of Medicine, who presented her findings at the American Association for Cancer Research San Antonio Breast Cancer Symposium.
A team at the Massachusetts Institute of Technology and the Broad Institute in August reported a similar finding in breast cancer cells and in mice in the journal Cell.
In the latest study, supported by funding from Merck, Chang and colleagues injected mice with breast cancer cells taken from patients and grew human tumours in the mice that were identical to those growing in women.
The team then studied the specific properties of the cancer stem cells, and focused on the Notch pathway, which is important for normal development of breast tissue.
"We found this was also active in cancer stem cells," Chang said in a telephone interview.
Chang said breast cancer stem cells were dependent on the Notch pathway for survival. Merck's drug MK-0752, a compound called a gamma-secretase inhibitor, blocks that pathway.
When the team combined the drug with regular chemotherapy in mice, "we found we managed to hit cancer stem cells," Chang said.
The compound also is working in a study involving 35 women with advanced breast cancer. Breast cancer biopsies before and after treatment show it reduces the number of breast cancer stem cells. "We do see responses. After a period of time, the tumours regress, but more importantly, we are attacking the cancer stem cell component," Chang said.