Engineer stem cells to study leukemia better

In order to better understand the mechanisms behind a form of leukemia caused by changes in a key gene, scientists engineered stem cells for leukemia. The study was led by Mount Sinai researchers and published in the journal Cell Reports online.
Before then, it had been established that inherited changes in the DNA code for the gene PTPN11 cause Noonan syndrome, a genetic disease that comes with a high risk for the blood cancer called juvenile myelomonocytic leukemia (JMML). Scientists still didn't know the mechanisms behind the disease and what influences its severity.
What's worse, currently the only treatment for JMML - a bone marrow transplant to replace the hematopoietic stem cells that become blood cells - is effective only in 50% of patients. This pushes scientists to step more toward designing better treatments.
"By studying an inherited human cancer syndrome, our study clarified early events in the development of one kind of leukemia," said corresponding study author Bruce D. Gelb, MD, Gogel Family Chair and Director of The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai. "More than just creating a model of a disease, we were able to prove that mechanisms seen in our model also happen in the bone marrow of people with this kind of leukemia. The work also provided new targets for the field to develop new drugs against in JMML."
In order to better understand diseases with a genetic component, scientists choose the approach of taking skin cells from patients with a disease and use enzymes to coax the cells back along the differentiation pathway to become induced pluripotent stem cells or iPSCs. Such cells can then be programmed to mature into cells including hematopoietic (blood) cells, which re-create a specific version of each person's genetic disease in a petri dish for study.
In the study, authors say that hematopoietic cells produced from induced stem cells with PTPN11 mutations known to cause JMML indeed act like cells seen in these patients. According to them, "gain of function" genetic changes that happen to increase this protein's expression were enough to cause leukemia-related changes in cells.
iPSCs used to model cancers are often created from cancer cells, a process with comes with a great many mutations (changes in the gene code) in genes that are part of the unstable, frequent cell division and multiplication seen in cancer. By starting with skin cells of JMML patients with inherited PTPN11 mutations, scientists could create JMML cells with only these mutations, screening out the "genetic noise" that can obscure disease mechanisms.
The results of the study show that the severity of this form of leukemia arises from the degree of changes in the gene PTPN11, altering the protein it codes for, SHP-2, and biologic pathways related to it. And these proteins promise to become a focus of future drug design efforts, According to Dr. Gelb.
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