TY - JOUR
T1 - Butyric acid
T2 - Inhibition of non-leukemic and chronic myeloid leukemia granulocyte macrophage clonal growth
AU - Januszewicz, Elchanan
AU - Rabizadah, Esther
AU - Novogrodsky, Abraham
AU - Shaklai, Matityahu
PY - 1988/12
Y1 - 1988/12
N2 - Butyric acid has been shown to inhibit the growth of several established tumor cell lines and to induce either granulocytic or erythroid differentiation in different human and murine leukemic cell lines. The dose-dependent effect of butyric acid was tested in vitro on the clonal growth of granulocyte macrophage progenitors in 13 patients with chronic myeloid leukemia (CML) and compared with control bone marrow and peripheral blood responses. The growth of myeloid progenitors from both healthy donors and non-leukemic and leukemic patients was almost completely inhibited by 1.0 mM butyric acid. At 0.5 mM butyric acid, inhibition of CML progenitors, both from chronic phase and blastic phase patients, was significantly greater (P < 0.01) than bone marrow from non-leukemic patients and peripheral blood controls. Butyric acid, a 4-carbon compound, was the most potent inhibitor of six short chain fatty acids tested on CML myeloid progenitors.
AB - Butyric acid has been shown to inhibit the growth of several established tumor cell lines and to induce either granulocytic or erythroid differentiation in different human and murine leukemic cell lines. The dose-dependent effect of butyric acid was tested in vitro on the clonal growth of granulocyte macrophage progenitors in 13 patients with chronic myeloid leukemia (CML) and compared with control bone marrow and peripheral blood responses. The growth of myeloid progenitors from both healthy donors and non-leukemic and leukemic patients was almost completely inhibited by 1.0 mM butyric acid. At 0.5 mM butyric acid, inhibition of CML progenitors, both from chronic phase and blastic phase patients, was significantly greater (P < 0.01) than bone marrow from non-leukemic patients and peripheral blood controls. Butyric acid, a 4-carbon compound, was the most potent inhibitor of six short chain fatty acids tested on CML myeloid progenitors.
KW - Butyric acid
KW - CFU-GM
KW - Chronic myeloid leukemia
UR - http://www.scopus.com/inward/record.url?scp=0023733153&partnerID=8YFLogxK
U2 - 10.1007/BF03003194
DO - 10.1007/BF03003194
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C2 - 3193830
AN - SCOPUS:0023733153
SN - 0736-0118
VL - 5
SP - 259
EP - 263
JO - Medical Oncology and Tumor Pharmacotherapy
JF - Medical Oncology and Tumor Pharmacotherapy
IS - 4
ER -