Sensitization to X ray by 5-chloro-2′-deoxycytidine co-administered with tetrahydrouridine in several mammalian cell lines and studies of 2′-chloro derivatives

Liliana M. Perez, Sheldon Greer

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

5-Chloro-2′-deoxycytidine (CIdC) + tetrahydrouridine (H4U) sensitizes mammalian cells (HEp-2, RIF-1, 5-180) to X ray. This sensitization, as demonstrated previously with HEp-2 cells, is heightened when cells are pre-incubated with inhibitors of pyrimidine synthesis. CHO cells, which intrinsically lack both cytidine deaminase (CD) and deoxycytidylate deaminase (dCMPD), are sensitized to X ray by 5-chlorodeoxyuridine (CIdU) but display no significant sensitization with CIdC + H4U. The presence and level of these deaminases appears to correlate with X ray sensitization in cell culture. From experiments in cell culture, it can be inferred that one pathway of conversion, (a) deoxycytidine kinase → dCMPD, or (b) CD → thymidine kinase, may be sufficient for metabolizing C1dC to a radiosensitizer. However, if both pathways are blocked, as in CHO cells, no X ray sensitization results. In addition to HEp-2 cells, which are extremely elevated in both CD and dCMPD activities, we have examined the sensitization of S-180 and RIF-1 cells to X ray by CIdC + H4U. Both cell lines possess an enzymatic profile consistent with their sensitization to X ray by CIdC + H4U. Dose enhancement ratios of 1.5 to 1.9 for cells treated with CIdC + H4U + H4U and ratios of 2.0-2.7 for cells pre-treated with inhibitors of pyrimidine synthesis prior to CldC + H4U have been obtained. Based on reports of the marked X ray sensitization of bacteria by 2′-chloro-2′-deoxythymidine, we obtained 2′,5-dichloro-2′-deoxycytidine and 5-bromo-2'-chloro-2-deoxycytdine and found these analogs to be X ray sensitizers of mammalian cells. The strategy that we propose with CIdC + H4U and the related 2'-chloro derivatives, based on the elevation of CD and dCMPD in human tumors, offers a degree of selectivity that is not necessarily related to differences in cell kinetics; such that malignancies other than brain tumors may be amenable to this therapy.

Original languageEnglish
Pages (from-to)1523-1527
Number of pages5
JournalInternational journal of radiation oncology, biology, physics
Volume12
Issue number8
DOIs
StatePublished - Jan 1 1986
Externally publishedYes

Fingerprint

Tetrahydrouridine
cultured cells
X-Rays
Cell Line
Cytidine Deaminase
cells
x rays
CHO Cells
pyrimidines
inhibitors
Bromodeoxycytidine
DCMP Deaminase
tumors
Cell Culture Techniques
Deoxycytidine Kinase
5-chloro-2'-deoxycytidine
thymidine
Thymidine Kinase
synthesis
Brain Neoplasms

Keywords

  • 2′
  • 5-Bromo-2′-chloro-2′-deoxyuridine (5-Br-2′-C1dU)
  • 5-Chloro-2′-deoxycytidine (CIdC)
  • 5-CldC)
  • 5-dichloro-2′-deoxycytidine (2′
  • Cytidine deaminase (CD)
  • Deoxycytidine kinase (dCK)
  • Deoxycytidylate deaminase (dCMPD)
  • Tetrahydrouridine (HU)
  • Tumor-selective
  • X ray sensitization

ASJC Scopus subject areas

  • Oncology
  • Radiology Nuclear Medicine and imaging
  • Radiation

Cite this

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title = "Sensitization to X ray by 5-chloro-2′-deoxycytidine co-administered with tetrahydrouridine in several mammalian cell lines and studies of 2′-chloro derivatives",
abstract = "5-Chloro-2′-deoxycytidine (CIdC) + tetrahydrouridine (H4U) sensitizes mammalian cells (HEp-2, RIF-1, 5-180) to X ray. This sensitization, as demonstrated previously with HEp-2 cells, is heightened when cells are pre-incubated with inhibitors of pyrimidine synthesis. CHO cells, which intrinsically lack both cytidine deaminase (CD) and deoxycytidylate deaminase (dCMPD), are sensitized to X ray by 5-chlorodeoxyuridine (CIdU) but display no significant sensitization with CIdC + H4U. The presence and level of these deaminases appears to correlate with X ray sensitization in cell culture. From experiments in cell culture, it can be inferred that one pathway of conversion, (a) deoxycytidine kinase → dCMPD, or (b) CD → thymidine kinase, may be sufficient for metabolizing C1dC to a radiosensitizer. However, if both pathways are blocked, as in CHO cells, no X ray sensitization results. In addition to HEp-2 cells, which are extremely elevated in both CD and dCMPD activities, we have examined the sensitization of S-180 and RIF-1 cells to X ray by CIdC + H4U. Both cell lines possess an enzymatic profile consistent with their sensitization to X ray by CIdC + H4U. Dose enhancement ratios of 1.5 to 1.9 for cells treated with CIdC + H4U + H4U and ratios of 2.0-2.7 for cells pre-treated with inhibitors of pyrimidine synthesis prior to CldC + H4U have been obtained. Based on reports of the marked X ray sensitization of bacteria by 2′-chloro-2′-deoxythymidine, we obtained 2′,5-dichloro-2′-deoxycytidine and 5-bromo-2'-chloro-2-deoxycytdine and found these analogs to be X ray sensitizers of mammalian cells. The strategy that we propose with CIdC + H4U and the related 2'-chloro derivatives, based on the elevation of CD and dCMPD in human tumors, offers a degree of selectivity that is not necessarily related to differences in cell kinetics; such that malignancies other than brain tumors may be amenable to this therapy.",
keywords = "2′, 5-Bromo-2′-chloro-2′-deoxyuridine (5-Br-2′-C1dU), 5-Chloro-2′-deoxycytidine (CIdC), 5-CldC), 5-dichloro-2′-deoxycytidine (2′, Cytidine deaminase (CD), Deoxycytidine kinase (dCK), Deoxycytidylate deaminase (dCMPD), Tetrahydrouridine (HU), Tumor-selective, X ray sensitization",
author = "Perez, {Liliana M.} and Sheldon Greer",
year = "1986",
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doi = "10.1016/0360-3016(86)90208-7",
language = "English",
volume = "12",
pages = "1523--1527",
journal = "International Journal of Radiation Oncology Biology Physics",
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TY - JOUR

T1 - Sensitization to X ray by 5-chloro-2′-deoxycytidine co-administered with tetrahydrouridine in several mammalian cell lines and studies of 2′-chloro derivatives

AU - Perez, Liliana M.

AU - Greer, Sheldon

PY - 1986/1/1

Y1 - 1986/1/1

N2 - 5-Chloro-2′-deoxycytidine (CIdC) + tetrahydrouridine (H4U) sensitizes mammalian cells (HEp-2, RIF-1, 5-180) to X ray. This sensitization, as demonstrated previously with HEp-2 cells, is heightened when cells are pre-incubated with inhibitors of pyrimidine synthesis. CHO cells, which intrinsically lack both cytidine deaminase (CD) and deoxycytidylate deaminase (dCMPD), are sensitized to X ray by 5-chlorodeoxyuridine (CIdU) but display no significant sensitization with CIdC + H4U. The presence and level of these deaminases appears to correlate with X ray sensitization in cell culture. From experiments in cell culture, it can be inferred that one pathway of conversion, (a) deoxycytidine kinase → dCMPD, or (b) CD → thymidine kinase, may be sufficient for metabolizing C1dC to a radiosensitizer. However, if both pathways are blocked, as in CHO cells, no X ray sensitization results. In addition to HEp-2 cells, which are extremely elevated in both CD and dCMPD activities, we have examined the sensitization of S-180 and RIF-1 cells to X ray by CIdC + H4U. Both cell lines possess an enzymatic profile consistent with their sensitization to X ray by CIdC + H4U. Dose enhancement ratios of 1.5 to 1.9 for cells treated with CIdC + H4U + H4U and ratios of 2.0-2.7 for cells pre-treated with inhibitors of pyrimidine synthesis prior to CldC + H4U have been obtained. Based on reports of the marked X ray sensitization of bacteria by 2′-chloro-2′-deoxythymidine, we obtained 2′,5-dichloro-2′-deoxycytidine and 5-bromo-2'-chloro-2-deoxycytdine and found these analogs to be X ray sensitizers of mammalian cells. The strategy that we propose with CIdC + H4U and the related 2'-chloro derivatives, based on the elevation of CD and dCMPD in human tumors, offers a degree of selectivity that is not necessarily related to differences in cell kinetics; such that malignancies other than brain tumors may be amenable to this therapy.

AB - 5-Chloro-2′-deoxycytidine (CIdC) + tetrahydrouridine (H4U) sensitizes mammalian cells (HEp-2, RIF-1, 5-180) to X ray. This sensitization, as demonstrated previously with HEp-2 cells, is heightened when cells are pre-incubated with inhibitors of pyrimidine synthesis. CHO cells, which intrinsically lack both cytidine deaminase (CD) and deoxycytidylate deaminase (dCMPD), are sensitized to X ray by 5-chlorodeoxyuridine (CIdU) but display no significant sensitization with CIdC + H4U. The presence and level of these deaminases appears to correlate with X ray sensitization in cell culture. From experiments in cell culture, it can be inferred that one pathway of conversion, (a) deoxycytidine kinase → dCMPD, or (b) CD → thymidine kinase, may be sufficient for metabolizing C1dC to a radiosensitizer. However, if both pathways are blocked, as in CHO cells, no X ray sensitization results. In addition to HEp-2 cells, which are extremely elevated in both CD and dCMPD activities, we have examined the sensitization of S-180 and RIF-1 cells to X ray by CIdC + H4U. Both cell lines possess an enzymatic profile consistent with their sensitization to X ray by CIdC + H4U. Dose enhancement ratios of 1.5 to 1.9 for cells treated with CIdC + H4U + H4U and ratios of 2.0-2.7 for cells pre-treated with inhibitors of pyrimidine synthesis prior to CldC + H4U have been obtained. Based on reports of the marked X ray sensitization of bacteria by 2′-chloro-2′-deoxythymidine, we obtained 2′,5-dichloro-2′-deoxycytidine and 5-bromo-2'-chloro-2-deoxycytdine and found these analogs to be X ray sensitizers of mammalian cells. The strategy that we propose with CIdC + H4U and the related 2'-chloro derivatives, based on the elevation of CD and dCMPD in human tumors, offers a degree of selectivity that is not necessarily related to differences in cell kinetics; such that malignancies other than brain tumors may be amenable to this therapy.

KW - 2′

KW - 5-Bromo-2′-chloro-2′-deoxyuridine (5-Br-2′-C1dU)

KW - 5-Chloro-2′-deoxycytidine (CIdC)

KW - 5-CldC)

KW - 5-dichloro-2′-deoxycytidine (2′

KW - Cytidine deaminase (CD)

KW - Deoxycytidine kinase (dCK)

KW - Deoxycytidylate deaminase (dCMPD)

KW - Tetrahydrouridine (HU)

KW - Tumor-selective

KW - X ray sensitization

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DO - 10.1016/0360-3016(86)90208-7

M3 - Article

VL - 12

SP - 1523

EP - 1527

JO - International Journal of Radiation Oncology Biology Physics

JF - International Journal of Radiation Oncology Biology Physics

SN - 0360-3016

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