TY - JOUR
T1 - Selective sensitivity to tiazofurin of human leukemic cells
AU - Jayarama, Hiremagalur N.
AU - Pillwein, Konrad
AU - Nichols, Craig R.
AU - Hoffman, Roland
AU - Weber, George
N1 - Funding Information:
Tiazofurin§ (2-fl-D-ribofuranosylthiazole-4-carboxamide) exhibits potent antitumor activity against murine tumors \[1, 2\] and is now undergoing Phase I trials \[3, 4\]. The mechanism of action of tiazofurin * The work was supported by Grants CA-05034 and CA-13526 from the United States Public Health Service, National Cancer Institute. $ Address correspondence to: Dr. George Weber, Laboratory for Experimental Oncology, Indiana University School of Medicine, 702 Barnhill Drive, Indianapolis, IN 46223. § Abbreviations: ALL, acute lymphoblastic leukemia; AMSA, amsacrine; ANLL, acute non-lymphocytic leukemia; ARA-C, cytosine arabinoside; DNR, daunorubicin; HDARA-C, high dose cytosine arabinoside; PRED, prednisone; TAD, thiazole-4-carboxamide adenine dinucleotide; TCA, trichloroacetic acid; 6-TG, 6-thioguanine; tiazofurin, 2-beta-D-ribofuranosylthiazole-4-carboxamide; TRMP, tiazofurin-5'-phosphate; VCR, vincristine; and VP-16, etoposid e.
PY - 1986/6/15
Y1 - 1986/6/15
N2 - This study reports the selective sensitivity to tiazofurin (2-beta-D-ribofuranosylthiazole-4-carboxamide, NSC-286193) of human leukemic leukocytes as compared to normal ones in bone marrow and peripheral blood samples by comparing the production of the active metabolite, thiazole-4-carboxamide adenine dinucleotide (TAD), from labeled tiazofurin and the depression of GTP concentration. When labeled tiazofurin was incubated with leukocytes obtained from healthy volunteers or from leukemic patients (acute non-lymphocytic leukemia or acute lymphoblastic leukemia), the TAD production was 27.0 +- 8.3, 551.3 +- 71.8 and 755.9 +- 94.1 pmoles/109 cells per hr, respectively. Thus, the leukemic cells produced over 20-fold higher concentrations of TAD than the normal leukocytes. Incibation with tiazofurin in leukemic leukocytes decreased the GTP pools (to 48-79%), whereas there was no change in the normal leukocytes. These results indicate a selectivity of response to tiazofurin in human normal and leukemic leukocytes. These procedure reported in this work may be suitable as a rapid predictive test for the sensitivity of leukemic leukocytes to tiazofurin. Such a diagnostic test should be helpful in identifying neoplastic cells sensitive to tiazofurin in the Phase II trials now being developed.
AB - This study reports the selective sensitivity to tiazofurin (2-beta-D-ribofuranosylthiazole-4-carboxamide, NSC-286193) of human leukemic leukocytes as compared to normal ones in bone marrow and peripheral blood samples by comparing the production of the active metabolite, thiazole-4-carboxamide adenine dinucleotide (TAD), from labeled tiazofurin and the depression of GTP concentration. When labeled tiazofurin was incubated with leukocytes obtained from healthy volunteers or from leukemic patients (acute non-lymphocytic leukemia or acute lymphoblastic leukemia), the TAD production was 27.0 +- 8.3, 551.3 +- 71.8 and 755.9 +- 94.1 pmoles/109 cells per hr, respectively. Thus, the leukemic cells produced over 20-fold higher concentrations of TAD than the normal leukocytes. Incibation with tiazofurin in leukemic leukocytes decreased the GTP pools (to 48-79%), whereas there was no change in the normal leukocytes. These results indicate a selectivity of response to tiazofurin in human normal and leukemic leukocytes. These procedure reported in this work may be suitable as a rapid predictive test for the sensitivity of leukemic leukocytes to tiazofurin. Such a diagnostic test should be helpful in identifying neoplastic cells sensitive to tiazofurin in the Phase II trials now being developed.
UR - https://www.scopus.com/pages/publications/0022533903
U2 - 10.1016/0006-2952(86)90737-9
DO - 10.1016/0006-2952(86)90737-9
M3 - Article
C2 - 3718544
AN - SCOPUS:0022533903
SN - 0006-2952
VL - 35
SP - 2029
EP - 2032
JO - Biochemical Pharmacology
JF - Biochemical Pharmacology
IS - 12
ER -