Induction of thymidine phosphorylase in both irradiated and shielded, contralateral human U87MG glioma xenografts: Implications for a dual modality treatment using capecitabine and irradiation

Carmelo Blanquicett, G. Yancey Gillespie, L. Burt Nabors, C. Ryan Miller, Sumen Bharara, Donald J. Buchsbaum, Robert B Diasio, Martin R. Johnson

Research output: Contribution to journalArticle

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Abstract

In the United States, tumors of the central nervous system remain the third leading cancer-related cause of death in young adults with a median survival time of <1 year. A recent case study suggested that Capecitabine (a novel, fluoropyrimidine prodrug) may be effective in the treatment of brain metastases. Pharmacogenomic studies have correlated the antitumor response to Capecitabine with the expression of the drug metabolizing enzymes thymidine phosphorylase (TP) and dihydropyrimidine dehydrogenase (DPD). In the current study, we examined TP and DPD expression in normal human brain tissues and in glioblastoma multiforme, the most common and malignant type of brain tumor. Because previous reports suggest a tumor necrosis factor (TNF)-α-mediated increase in TP expression after irradiation (a current standard of care for glioblastoma multiforme), we also examined the effect of irradiation on the expression of TP, DPD, and TNF-α in both irradiated and lead-shielded contralateral U87MG glioma xenografts within the same animal. Expression levels were determined using real-time quantitative PCR as described previously. Results demonstrate an ∼70-fold increase in TP mRNA levels 4 days after irradiation, relative to initial control levels. Interestingly, TP mRNA in the lead-shielded tumors (contralateral to irradiated tumors) increased ∼60-fold by day 10 relative to initial control levels. Elevated TP levels were sustained for 20 days in irradiated xenografts but began to decrease after 15 days in the shielded/contralateral tumors, returning to baseline by 20 days. TP mRNA levels in normal mouse liver were unaltered, suggesting a tumor-associated effect. TNF-α mRNA levels did not increase after irradiation; therefore, mRNA expression of 11 additional cytokines [interleukin (IL)-1α, IL-1β, IL-2, IL-4, IL-5, IL-8, IL-10, IL-12p35, IL-12p40, IL-15, and IFN-γ] in both the irradiated and shielded xenografts was quantitated. Results demonstrated increased levels of IFN-γ, IL-10, and IL-1α by 6.3-, 3.7-, and 1.6-fold, respectively, in irradiated tumors only. DPD mRNA levels did not change after irradiation. The tumor-associated induction of TP in irradiated and lead-shielded tumors within the same animal may have significant implications for the combined modality treatment of cancer patients with Capecitabine in conjunction with radiotherapy and may apply to the treatment of distant tumors and or metastatic disease.

Original languageEnglish (US)
Pages (from-to)1139-1145
Number of pages7
JournalMolecular Cancer Therapeutics
Volume1
Issue number12
StatePublished - Oct 2002
Externally publishedYes

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Thymidine Phosphorylase
Heterografts
Glioma
Dihydrouracil Dehydrogenase (NADP)
Neoplasms
Messenger RNA
Interleukin-1
Therapeutics
Tumor Necrosis Factor-alpha
Interleukins
Glioblastoma
Interleukin-10
Capecitabine
Interleukin-15
Central Nervous System Neoplasms
Interleukin-5
Prodrugs
Brain
Standard of Care
Interleukin-8

ASJC Scopus subject areas

  • Oncology
  • Cancer Research
  • Drug Discovery
  • Pharmacology

Cite this

Induction of thymidine phosphorylase in both irradiated and shielded, contralateral human U87MG glioma xenografts : Implications for a dual modality treatment using capecitabine and irradiation. / Blanquicett, Carmelo; Gillespie, G. Yancey; Nabors, L. Burt; Miller, C. Ryan; Bharara, Sumen; Buchsbaum, Donald J.; Diasio, Robert B; Johnson, Martin R.

In: Molecular Cancer Therapeutics, Vol. 1, No. 12, 10.2002, p. 1139-1145.

Research output: Contribution to journalArticle

Blanquicett, Carmelo ; Gillespie, G. Yancey ; Nabors, L. Burt ; Miller, C. Ryan ; Bharara, Sumen ; Buchsbaum, Donald J. ; Diasio, Robert B ; Johnson, Martin R. / Induction of thymidine phosphorylase in both irradiated and shielded, contralateral human U87MG glioma xenografts : Implications for a dual modality treatment using capecitabine and irradiation. In: Molecular Cancer Therapeutics. 2002 ; Vol. 1, No. 12. pp. 1139-1145.
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abstract = "In the United States, tumors of the central nervous system remain the third leading cancer-related cause of death in young adults with a median survival time of <1 year. A recent case study suggested that Capecitabine (a novel, fluoropyrimidine prodrug) may be effective in the treatment of brain metastases. Pharmacogenomic studies have correlated the antitumor response to Capecitabine with the expression of the drug metabolizing enzymes thymidine phosphorylase (TP) and dihydropyrimidine dehydrogenase (DPD). In the current study, we examined TP and DPD expression in normal human brain tissues and in glioblastoma multiforme, the most common and malignant type of brain tumor. Because previous reports suggest a tumor necrosis factor (TNF)-α-mediated increase in TP expression after irradiation (a current standard of care for glioblastoma multiforme), we also examined the effect of irradiation on the expression of TP, DPD, and TNF-α in both irradiated and lead-shielded contralateral U87MG glioma xenografts within the same animal. Expression levels were determined using real-time quantitative PCR as described previously. Results demonstrate an ∼70-fold increase in TP mRNA levels 4 days after irradiation, relative to initial control levels. Interestingly, TP mRNA in the lead-shielded tumors (contralateral to irradiated tumors) increased ∼60-fold by day 10 relative to initial control levels. Elevated TP levels were sustained for 20 days in irradiated xenografts but began to decrease after 15 days in the shielded/contralateral tumors, returning to baseline by 20 days. TP mRNA levels in normal mouse liver were unaltered, suggesting a tumor-associated effect. TNF-α mRNA levels did not increase after irradiation; therefore, mRNA expression of 11 additional cytokines [interleukin (IL)-1α, IL-1β, IL-2, IL-4, IL-5, IL-8, IL-10, IL-12p35, IL-12p40, IL-15, and IFN-γ] in both the irradiated and shielded xenografts was quantitated. Results demonstrated increased levels of IFN-γ, IL-10, and IL-1α by 6.3-, 3.7-, and 1.6-fold, respectively, in irradiated tumors only. DPD mRNA levels did not change after irradiation. The tumor-associated induction of TP in irradiated and lead-shielded tumors within the same animal may have significant implications for the combined modality treatment of cancer patients with Capecitabine in conjunction with radiotherapy and may apply to the treatment of distant tumors and or metastatic disease.",
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AU - Blanquicett, Carmelo

AU - Gillespie, G. Yancey

AU - Nabors, L. Burt

AU - Miller, C. Ryan

AU - Bharara, Sumen

AU - Buchsbaum, Donald J.

AU - Diasio, Robert B

AU - Johnson, Martin R.

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N2 - In the United States, tumors of the central nervous system remain the third leading cancer-related cause of death in young adults with a median survival time of <1 year. A recent case study suggested that Capecitabine (a novel, fluoropyrimidine prodrug) may be effective in the treatment of brain metastases. Pharmacogenomic studies have correlated the antitumor response to Capecitabine with the expression of the drug metabolizing enzymes thymidine phosphorylase (TP) and dihydropyrimidine dehydrogenase (DPD). In the current study, we examined TP and DPD expression in normal human brain tissues and in glioblastoma multiforme, the most common and malignant type of brain tumor. Because previous reports suggest a tumor necrosis factor (TNF)-α-mediated increase in TP expression after irradiation (a current standard of care for glioblastoma multiforme), we also examined the effect of irradiation on the expression of TP, DPD, and TNF-α in both irradiated and lead-shielded contralateral U87MG glioma xenografts within the same animal. Expression levels were determined using real-time quantitative PCR as described previously. Results demonstrate an ∼70-fold increase in TP mRNA levels 4 days after irradiation, relative to initial control levels. Interestingly, TP mRNA in the lead-shielded tumors (contralateral to irradiated tumors) increased ∼60-fold by day 10 relative to initial control levels. Elevated TP levels were sustained for 20 days in irradiated xenografts but began to decrease after 15 days in the shielded/contralateral tumors, returning to baseline by 20 days. TP mRNA levels in normal mouse liver were unaltered, suggesting a tumor-associated effect. TNF-α mRNA levels did not increase after irradiation; therefore, mRNA expression of 11 additional cytokines [interleukin (IL)-1α, IL-1β, IL-2, IL-4, IL-5, IL-8, IL-10, IL-12p35, IL-12p40, IL-15, and IFN-γ] in both the irradiated and shielded xenografts was quantitated. Results demonstrated increased levels of IFN-γ, IL-10, and IL-1α by 6.3-, 3.7-, and 1.6-fold, respectively, in irradiated tumors only. DPD mRNA levels did not change after irradiation. The tumor-associated induction of TP in irradiated and lead-shielded tumors within the same animal may have significant implications for the combined modality treatment of cancer patients with Capecitabine in conjunction with radiotherapy and may apply to the treatment of distant tumors and or metastatic disease.

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