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PubMed1977

Action of FdUrD and dCyd on the incorporation of BrdUrd in chinese hamster somatic cell DNA and the isolation of auxotrophic mutants.

Chinese hamster somatic cells grown in the presence of bromodeoxyuridine, deoxycytidine and fluorodeoxyuridine incorporate more bromodeoxyuridine in the DNA than cells grown in the presence of bromodeoxyuridine alone. Thus they become more sensitive to light irradiation. Our data suggest that 0.05 mM--0.2 mM bromodeoxyuridine, 0.05 mM deoxyctidine and 10 mmug/ml fluorodeoxyuridine is one of the best possible combinations for the selection of Chinese hamster somatic cells mutants. Auxotrophs for proline, inositol or both were thus isolated at high frequency.

Animals↗
PubMed1978

Thymidylate synthetase and dihydrofolic acid reductase in the stimulated human lymphocyte.

The phytohemagglutinin (PHA)-stimulated human lymphocytes demonstrated trace or no activity (dihydro) folate acid reductase using three methods including a radioassay, but demonstrated ample activity of thymidylate synthetase. This was true regardless of the day of harvest, (first through seventh) of the stimulated lymphocyte. The lymphocyte extracts revealed no inhibitor to the reductase enzyme when these extracts were added before the liver extracts to the assay system. When methotrexate (MTX) was added to the culture media of the lymphocytes, there was, as expected, an increase in the synthetase activity, but the expected rise in the reductase activity did not occur, it remained nil. On the other hand, MTX did influence the incorporation of nucleosides by the stimulated lymphocytes in a fashion similar to its action on the incorporation of the same nucleosides by other cells.

Cells, Cultured↗
PubMed1979

alpha-Amanitin and 5-fluorouridine inhibition of serum-stimulated DNA synthesis in quiescent AKR-2B mouse embryo cells.

AKR-2B mouse embryo cells undergoing the serum-stimulated transition from a quiescent to a proliferating state exhibit an increase in the rate of hnRNA synthesis which appears to be mediated through an increase in the actual number of RNA polymerase II molecules. alpha-Amanitin, administered early in the prereplication interval following stimulation, effectively inhibits hnRNA synthesis, polysomal mRNA accumulation, polyribosome formation, and subsequent DNA synthesis, and cell division. Unexpectedly, alpha-amanitin treatment also produces almost complete inhibition of the synthesis of 45S rRNA precursor and the increase in accumulation of cytoplasmic rRNA following serum stimulation. In order to determine whether the inhibition of new ribosomal synthesis might in itself be sufficient to prevent serum-stimulated DNA synthesis, the effects of 5-fluorouridine (5-FU), a specific inhibitor of 45S rRNA processing, were investigated. If added within eight hours following serum stimulation, 5-FU was found to completely inhibit subsequent DNA synthesis. These results suggest that quiescent AKR-2B cells do not contain a sufficient excess of ribosomes to support the synthesis of proteins which are required for DNA synthesis in response to serum growth factors. Furthermore, an early polymerase II mediated synthesis of mRNA(s) coding for some factor(s) necessary for ribosomal gene transcription may be an essential step in the serum-stimulated synthesis of new ribosomes.

Amanitins↗
PubMed1977

Defective transport of thymidine by cultured cells resistant to 5-bromodeoxyuridine.

A line of HeLa cells resistant to 5-bromo-2'-deoxyuridine (BUdR) was established by continuous culture in growth medium containing BUdR; during the selection period, BUdR concentrations, initially 15 micrometer, were gradually increased to 100 micrometer. Cells of a clone (HeLa/B5) established from this line were also resistant to 5-fluoro-2'-deoxyuridine (FUdR), but not to the free base, 5-fluorouracil. Although extracts of HeLa/B5 cells exhibited levels of thymidine kinase activity comparable to those of parental cells, rates of uptake of BUdR, FUdR, and thymidine into intact cells were much reduced. The kinetics of uptake of uridine and adenosine, nucleosides which appear to be transported independently of thymidine in HeLa cells, were similar for HeLa/B5 and the parental line (HeLa/O). Relative to thymidine uptake by HeLa/O cells, that by HeLa/B5 cells was distinctly less sensitive to nitrobenzylthioinosine (NBMPR), a specific inhibitor of nucleoside transport in various types of animal cells. Despite this difference in NBMPR sensitivity, both cell lines possessed the same number of high affinity NBMPR binding sites per mg cell protein. The altered kinetics of thymidine uptake and the NBMPR insensitivity of that function in HeLA/B5 cells suggest that resistance to BUdR is due to an altered thymidine transport mechanism.

Biological Transport, Active↗
PubMed1978

Nonsystemic treatment of metastatic tumors of the liver--a review.

Hepatic metastasis is usually quite resistant to conventional systemic chemotherapy. Nonsystemic treatment of metastatic tumors of the liver include surgical resection; infusion of chemotherapeutic agent(s), either via hepatic artery or portal vein; ligation of hepatic artery; radiotherapy; and other more investigative approaches (isolation perfusion, cryosurgery, liver transplantation, etc). The relative applicability, results, and limitations of each of these therapeutic modalities are reviewed.

Antineoplastic Agents↗
PubMed1975

The effects of 5-fluorouracil and 5-fluorodeoxyuridine used alone and in combination with normal nucleic acid precursors on development of mice in lines selected for low and high expression of Strong's luxoid gene.

Pregnant female mice selected for plus- and minus-modifying genes of the limb-skeleton effects of Strong's luxoid gene (1st) were injected ip on day 10 of gestation with 10 or 20 mg/kg 5-fluorouracil (5-FU) or 5-fluorodeoxyuridine (5-FUdR). The incidence and degree of expression of the effects (polydactyly, ectrodactyly, radial hemimelia, tibial hemimelia, pelvic girdle shifts, deformed caudal vertebrae) varied according to the teratogen and dose level. The addition of an equimolecular amount of thymidine, thymine, or uracil greatly potentiated the effects of 20 mg/kg 5-FU, usually resulting in death of the embryos. The addition of an equimolecular amount of thymidine but not of the embryos. The addition of an equimolecular amount of thymidine but not of thymine or uracil partly protected against the effects of 5-FUdR. Both teratogens increased the expression of ist on the limb skeleton. The interactions of the teratogens with the major gene were inhibited by minus- and promoted by plus-modifying genes of 1st. The effects of the teratogenic treatments may be mediated by cell death.

Abnormalities, Drug-Induced↗
PubMed1978

Ultrastructural observations on FUdR-induced cell death and subsequent elimination of cell debris.

Twelve-day mouse embryos were treated with fluorodeoxyuridine (FUdR) and sacrificed at various time intervals after treatment. The neuroepithelial cells were then examined to determine by electron microscopy the primary site of action of the drug. About two hours after treatment mitotic activity ceased and a number of cells were found with a normal interphase nucleus, but with a cytoplasm in which the ribosomes had lost their normal polysomal configuration and were dispersed as single ribosomes. At about the same time cells were seen with an accumulation of chromatin at the nuclear membrane and the segregation of chromatin masses within the somewhat denser karyoplasm. Concurrent with the nuclear changes was the appearance of a condensed cytosome containing monoribosomes. The condensation of the nucleus and cytoplasm was followed by fragmentation of the cell into membrane bound bodies. Since condensed cells always contained monodispersed ribosomes, it seems likely that the dispersal of the ribosomes is the first morphological sign of the action of FUdR. Since about half of the neuroepithelial population underwent cell degeneration, the second goal of this experiment was to study the fate of the dying cells. Some fragments from condensed cells were found within apparently normal neuroepithelial cells, indicating phagocytosis. In addition macrophages were seen containing phagosomes from fragmented cells. Most of the fragments, however, remained free and were not immediately phagocytosed. These unphagocytosed fragments lysed and became ghosts, thereby giving the neureopithlium a vacuolated appearance. Hence, cellular debris was eliminated partially by neuroepithelial cells, partially by macrophages and to a great extent by lysis.

Animals↗
PubMed1975

DNA replication in the amphibia.

Autoradiographic techniques were used to measure rate of replication and length of the replication unit in cultured cells of Scaphiopus couchi, Bufo cognatus, Rana clamitans, and Triturus viridescens, having nuclear DNA amounts in the ratio 1:4:7:39 respectively. The autoradiographic experiments were designed to show whether the larger amounts of nuclear DNA are correlated with more rapid rates of synthesis and/or with longer replication units. -- The DNA replication rate was 2.5 mu/minute (corrected for two growing points) with 10 minutes 3H-thymidine label at 22 degrees C, but decreased with longer labelling durations. The length of the replication unit (estimated by the distance from the center of one autoradiograph to the center of the next in sequence) was most commonly in the 10-25 mu range with a 30 minute label, in all four species. The average center-to-center distance was 8 mu at 10 minutes and increased with label duration, to over 45 mu with 24 hours label. Replication was predominantly but not exclusively bidirectional. Neither rate of replication nor length of the replication unit was proportional to the amount of DNA in these species.

Amphibians↗
PubMed1976

[Effect of trenimon on single phases of the cell cycle of Yoshida ascites tumor cells (author's transl)].

Yoshida ascites tumor cells were synchronized in suspension cultures with thymidine in excess or with fluordeoxyuridine. Cells were washed after incubation with thymidine or treated with thymidine after incubation with fluordeoxyuridine. 2 h after terminating the S phase blockade 74--80% of the cells are S phase cells, 6 h later 70--80% of the cells had accumulated in the G 2 phase. Cultures enriched with cells of the S phase or the G 2 phase were treated with Trenimon. Increase of cell numbers within the following 48 h was inhibited in both cases in the same order of magnitude. In addition cells in various phases of growth were separated by density gradient zentrifugation and treated with Trenimon. Again cell numbers after 48 h were identical.

Animals↗
PubMed1978

Comparison of thymidine, fluorodeoxyuridine, hydroxyurea, and methotrexate blocking at the G1/S phase transition of the cell cycle, studied by replication patterns.

Cultures of human amniotic fluid cells and fibroblasts were temporarily blocked by the replication inhibitors thymidine (dT) surplus, fluorodeoxyuridine (FdU), hydroxyurea (HU), or methotrexate uridine (MU). The respective arresting point at G1-S transition and the homogeneity of the blocked cell population were determined by means of BrdU replication patterns. Most variation of patterns were found after HU. After MU, cells were arrested before the onset of replication, while with dT surplus of FdU an arresting point in early S seemed more likely.

Amniotic Fluid↗
PubMed1977

Replication of chromosomal DNA in diploid Drosophila melanogaster cells cultured in vitro.

Replication rate and replicon sizes in chromosomal DNA of in vitro cultured diploid D. melanogaster cells were determined using autoradiography of 3H-thymidine labeled DNA. Synthesis of DNA in euchromatic and heterochromatic regions of Drosophila diploid cells occurs at different periods of the S phase which last 10 h. During the first 4 h the synthesis is observed only in euchromatic regions. The heterochromatic synthesis starts shortly before the synthesis in euchromatic regions is completed and lasts for 6 h until the end of the S phase. The cells were synchronized by 5-fluorodeoxyuridine which blocked the diploid cell DNA synthesis. Synthesis was found to start simultaneously in most euchromatic replicons. In the majority of the replicons the synthesis started at a single point and proceeded bidirectionally. The average rate of DNA synthesis per fork was 12.5 mum/h (38kb). The mean distance between the middle points of adjacent labeled regions was 70 mgm (210 kb). The size of most replicons ranged from 40 to 120 mum. - These estimates do not apply to the heterochromatic portions of the D. melanogaster genome since the measurements have been carried out on DNA preparations obtained during the first 2 h of the S phase. - On the average, a replicon can consist of 7 chromomeres since the size of a replicon in diploid cell chromosomal DNA and DNA length of a polytene chromomere average 210 and 30 kb, respectively.

Animals↗