» Articles » PMID: 3285345

Prognostic Significance of "short-term" Effects of Chemotherapy on MYC and Histone H3 MRNA Levels in Acute Leukemia Patients

Overview
Specialty Science
Date 1988 May 1
PMID 3285345
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

We have found that administration of chemotherapy alters expression of growth-regulated genes in leukemia blast cells. To determine if such changes might be correlated with therapeutic outcome, we studied steady-state mRNA levels of MYC and histone H3 in the leukemic blasts of patients just prior to and 24 hr after the administration of the first doses of antileukemic drug therapy. Among nine patients with acute myelogenous leukemia, mRNA levels of MYC and histone H3 were reduced in five patients, and hematologic remission was achieved in three of these individuals. No remission was obtained in the four patients without reduction in MYC and histone H3 mRNA. Among acute lymphocytic leukemia patients, the mRNA levels of MYC and/or histone H3 were reduced by the therapy in seven of nine patients. A complete hematologic remission was obtained in five of them, and a partial remission was obtained in the other two. No remission was obtained in the patients in which MYC and H3 mRNA levels were unaffected by the therapy. These studies are of interest because they suggest that a decrease in the mRNA levels of MYC and histone H3 24 hr after a single dose of antineoplastic drugs may predict which patients will achieve complete remission; lack of reduction in these mRNAs correlates with failure to achieve remission. In addition, these studies also provide further proof of the heterogeneity of altered growth regulation among human leukemias.

Citing Articles

MiR-449a-5p mediates mitochondrial dysfunction and phenotypic transition by targeting Myc in pulmonary arterial smooth muscle cells.

Zhang C, Ma C, Zhang L, Zhang L, Zhang F, Ma M J Mol Med (Berl). 2019; 97(3):409-422.

PMID: 30715622 DOI: 10.1007/s00109-019-01751-7.


Histone H4 expression is cooperatively maintained by IKKβ and Akt1 which attenuates cisplatin-induced apoptosis through the DNA-PK/RIP1/IAPs signaling cascade.

Wang R, Zheng X, Zhang L, Zhou B, Hu H, Li Z Sci Rep. 2017; 7:41715.

PMID: 28139737 PMC: 5282510. DOI: 10.1038/srep41715.


Molecular characterization of the in vivo alkylating agent resistant murine EMT-6 mammary carcinoma tumors.

Chatterjee D, Liu C, Northey D, Teicher B Cancer Chemother Pharmacol. 1995; 35(5):423-31.

PMID: 7850925 DOI: 10.1007/s002800050257.


Mdr1/P-glycoprotein, topoisomerase, and glutathione-S-transferase pi gene expression in primary and relapsed state adult and childhood leukaemias.

Gekeler V, FRESE G, Noller A, Handgretinger R, Wilisch A, Schmidt H Br J Cancer. 1992; 66(3):507-17.

PMID: 1355660 PMC: 1977945. DOI: 10.1038/bjc.1992.304.

References
1.
Oudet P, Chambon P . Isolation of high-molecular-weight DNA from mammalian cells. Eur J Biochem. 1973; 36(1):32-8. DOI: 10.1111/j.1432-1033.1973.tb02881.x. View

2.
Torelli U, Selleri L, Venturelli D, Donelli A, Emilia G, Ceccherelli G . Differential patterns of expression of cell cycle-related genes in blast cells of acute myeloid leukemia. Leuk Res. 1986; 10(10):1249-54. DOI: 10.1016/0145-2126(86)90244-4. View

3.
Bennett J, Catovsky D, Daniel M, Flandrin G, GALTON D, Gralnick H . Proposals for the classification of the acute leukaemias. French-American-British (FAB) co-operative group. Br J Haematol. 1976; 33(4):451-8. DOI: 10.1111/j.1365-2141.1976.tb03563.x. View

4.
Rigby P, Dieckmann M, Rhodes C, Berg P . Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I. J Mol Biol. 1977; 113(1):237-51. DOI: 10.1016/0022-2836(77)90052-3. View

5.
Wahl G, Stern M, Stark G . Efficient transfer of large DNA fragments from agarose gels to diazobenzyloxymethyl-paper and rapid hybridization by using dextran sulfate. Proc Natl Acad Sci U S A. 1979; 76(8):3683-7. PMC: 383897. DOI: 10.1073/pnas.76.8.3683. View