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Volumn 27, Issue 4 B, 2007, Pages 2365-2375

Effects of tumor necrosis factor-related apoptosis-inducing ligand alone and in combination with fluoropyrimidine anticancer agent, S-1, on tumor growth of human oral squamous cell carcinoma xenografts in nude mice

Author keywords

Apoptosis; Combination therapy; Nude mice; Oral squamous cell carcinoma; S 1; TRAIL; TUNEL; Xenografts

Indexed keywords

5 CHLORO 2,4 DIHYDROXYPYRIDINE PLUS OXONATE POTASSIUM PLUS TEGAFUR; DIHYDROPYRIMIDINE DEHYDROGENASE; FLUOROPYRIMIDINE; OROTATE PHOSPHORIBOSYLTRANSFERASE; THYMIDYLATE SYNTHASE; TUMOR NECROSIS FACTOR RELATED APOPTOSIS INDUCING LIGAND;

EID: 34547786145     PISSN: 02507005     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (8)

References (35)
  • 1
    • 0029835349 scopus 로고    scopus 로고
    • Development of a novel form of 5-fluorouracil derivative (S-1) directed to the potentiation of the tumor-selective cytotoxicity of 5-fluorouracil by two biochemical modulators
    • Shirasaka T, Shimamoto Y, Ohshimo H, Yamaguchi M, Kato T, Yonekura K and Fukushima M: Development of a novel form of 5-fluorouracil derivative (S-1) directed to the potentiation of the tumor-selective cytotoxicity of 5-fluorouracil by two biochemical modulators. Anticancer Drugs 7: 548-557, 1996.
    • (1996) Anticancer Drugs , vol.7 , pp. 548-557
    • Shirasaka, T.1    Shimamoto, Y.2    Ohshimo, H.3    Yamaguchi, M.4    Kato, T.5    Yonekura, K.6    Fukushima, M.7
  • 2
    • 0023250474 scopus 로고
    • Inhibitory effects of pyrimidine, barbituric acid and pyridine derivatives on 5-fluorouracil degradation in rat liver extract
    • Tatsumi K, Fukushima M, Shirasaka T and Fujii S: Inhibitory effects of pyrimidine, barbituric acid and pyridine derivatives on 5-fluorouracil degradation in rat liver extract. Jpn J Cancer Res 78: 748-755, 1987.
    • (1987) Jpn J Cancer Res , vol.78 , pp. 748-755
    • Tatsumi, K.1    Fukushima, M.2    Shirasaka, T.3    Fujii, S.4
  • 3
    • 0027227591 scopus 로고
    • Inhibition of oxonic acid on gastrointestinal toxicity of 5-fluorouracil without loss of its antitumor activity in rats
    • Shirasaka T, Shimamoto Y and Fukushima M: Inhibition of oxonic acid on gastrointestinal toxicity of 5-fluorouracil without loss of its antitumor activity in rats. Cancer Res 53: 4004-4009, 1993.
    • (1993) Cancer Res , vol.53 , pp. 4004-4009
    • Shirasaka, T.1    Shimamoto, Y.2    Fukushima, M.3
  • 4
    • 9344248389 scopus 로고    scopus 로고
    • Antitumor effect of 1 M tegafur-0.4 M 5-chloro-2, 4-dihydroxypyridine-1 M potassium oxonate (S-1) against human colon carcinoma orthotopically implanted into nude rats
    • Shirasaka T, Nakano K, Takechi T, Satake H, Uchida J, Fujioka A, Nakano K, Ohshimo H, Takeda S and Shirasaka T: Antitumor effect of 1 M tegafur-0.4 M 5-chloro-2, 4-dihydroxypyridine-1 M potassium oxonate (S-1) against human colon carcinoma orthotopically implanted into nude rats. Cancer Res 56: 2602-2606, 1996.
    • (1996) Cancer Res , vol.56 , pp. 2602-2606
    • Shirasaka, T.1    Nakano, K.2    Takechi, T.3    Satake, H.4    Uchida, J.5    Fujioka, A.6    Nakano, K.7    Ohshimo, H.8    Takeda, S.9    Shirasaka, T.10
  • 5
    • 0032189218 scopus 로고    scopus 로고
    • Late Phase II study of novel oral fluoropyrimidine anticancer drug S-1 (1 M tegafur-0.4 M gimestat-1 M otastat potassium) in advanced gastric cancer patients
    • Sakata Y, Ohtsu A, Horikoshi N, Sugimachi K, Mitachi Y and Taguchi T: Late Phase II study of novel oral fluoropyrimidine anticancer drug S-1 (1 M tegafur-0.4 M gimestat-1 M otastat potassium) in advanced gastric cancer patients. Eur J Cancer 34: 1715-1720, 1998.
    • (1998) Eur J Cancer , vol.34 , pp. 1715-1720
    • Sakata, Y.1    Ohtsu, A.2    Horikoshi, N.3    Sugimachi, K.4    Mitachi, Y.5    Taguchi, T.6
  • 6
    • 0034089123 scopus 로고    scopus 로고
    • Phase II study of S-1, a novel oral fluoropyrimidine derivative, in patients with metastatic colorectal carcinoma
    • Ohtsu A, Baba H, Sakata Y, Mitachi Y, Horikoshi N, Sugimachi K and Taguchi T: Phase II study of S-1, a novel oral fluoropyrimidine derivative, in patients with metastatic colorectal carcinoma. Br J Cancer 83: 141-145, 2000.
    • (2000) Br J Cancer , vol.83 , pp. 141-145
    • Ohtsu, A.1    Baba, H.2    Sakata, Y.3    Mitachi, Y.4    Horikoshi, N.5    Sugimachi, K.6    Taguchi, T.7
  • 7
    • 0035964611 scopus 로고    scopus 로고
    • S-1 Cooperative Study Group (Lung Cancer Working Group), Phase II study of S-1, a novel oral fluorouracil, in advanced non-small cell lung cancer
    • Kawahara M, Furuse K, Segawa Y, Yoshimori K, Matsui K, Kudoh S, Hasegawa K and Niitani H: S-1 Cooperative Study Group (Lung Cancer Working Group), Phase II study of S-1, a novel oral fluorouracil, in advanced non-small cell lung cancer. Br J Cancer 85: 939-943, 2001.
    • (2001) Br J Cancer , vol.85 , pp. 939-943
    • Kawahara, M.1    Furuse, K.2    Segawa, Y.3    Yoshimori, K.4    Matsui, K.5    Kudoh, S.6    Hasegawa, K.7    Niitani, H.8
  • 8
    • 0035489130 scopus 로고    scopus 로고
    • Late phase II study of S-1 in patients with advanced head and neck cancer
    • Inuyama Y, Kida A, Tsukuda M, Kohno N and Satake B: Late phase II study of S-1 in patients with advanced head and neck cancer. Gan To Kagaku Ryoho 28: 1381-1390, 2001.
    • (2001) Gan To Kagaku Ryoho , vol.28 , pp. 1381-1390
    • Inuyama, Y.1    Kida, A.2    Tsukuda, M.3    Kohno, N.4    Satake, B.5
  • 9
    • 0038579652 scopus 로고    scopus 로고
    • EORTC Early Clinical Studies Group: Phase II trial with S-1 in chemotherapy-naive patients with gastric cancer. A trial performed by the EORTC Early Clinical Studies Group (ECSG)
    • Chollet P, Schoffski P, Weigang-Kohler K, Schellens JH, Cure H, Pavlidis N, Grunwald V, De Boer R, Wanders J and Fumoleau P; EORTC Early Clinical Studies Group: Phase II trial with S-1 in chemotherapy-naive patients with gastric cancer. A trial performed by the EORTC Early Clinical Studies Group (ECSG). Eur J Cancer 39: 1264-1270, 2003.
    • (2003) Eur J Cancer , vol.39 , pp. 1264-1270
    • Chollet, P.1    Schoffski, P.2    Weigang-Kohler, K.3    Schellens, J.H.4    Cure, H.5    Pavlidis, N.6    Grunwald, V.7    De Boer, R.8    Wanders, J.9    Fumoleau, P.10
  • 12
    • 0032575714 scopus 로고    scopus 로고
    • Death receptors: Signaling and modulation
    • Ashkenazi A and Dixit VM: Death receptors: signaling and modulation. Science 281: 1305-1308, 1998.
    • (1998) Science , vol.281 , pp. 1305-1308
    • Ashkenazi, A.1    Dixit, V.M.2
  • 14
    • 0033572413 scopus 로고    scopus 로고
    • Tumor necrosis factor-related apoptosis-inducing ligand's antitumor activity in vivo is enhanced by the chemotherapeutic agent CPT-11
    • Gliniak B and Le T: Tumor necrosis factor-related apoptosis-inducing ligand's antitumor activity in vivo is enhanced by the chemotherapeutic agent CPT-11. Cancer Res 59: 6153-6158, 1999.
    • (1999) Cancer Res , vol.59 , pp. 6153-6158
    • Gliniak, B.1    Le, T.2
  • 16
    • 0034652486 scopus 로고    scopus 로고
    • Increased death receptor 5 expression by chemotherapeutic agents in human gliomas causes synergistic cytotoxicity with tumor necrosis factor-related apoptosis-inducing ligand in vitro and in vivo
    • Nagane M, Pan G, Weddle JJ, Dixit VM, Cavenee WK and Huang HJ: Increased death receptor 5 expression by chemotherapeutic agents in human gliomas causes synergistic cytotoxicity with tumor necrosis factor-related apoptosis-inducing ligand in vitro and in vivo. Cancer Res 60: 847-853, 2000.
    • (2000) Cancer Res , vol.60 , pp. 847-853
    • Nagane, M.1    Pan, G.2    Weddle, J.J.3    Dixit, V.M.4    Cavenee, W.K.5    Huang, H.J.6
  • 17
    • 0034551746 scopus 로고    scopus 로고
    • Antileukemic drugs increase death receptor 5 levels and enhance Apo-2L-induced apoptosis of human acute leukemia cells
    • Wen J, Ramadevi N, Nguyen D, Perkins C, Worthington E and Bhalla K: Antileukemic drugs increase death receptor 5 levels and enhance Apo-2L-induced apoptosis of human acute leukemia cells. Blood 96: 3900-3906, 2000.
    • (2000) Blood , vol.96 , pp. 3900-3906
    • Wen, J.1    Ramadevi, N.2    Nguyen, D.3    Perkins, C.4    Worthington, E.5    Bhalla, K.6
  • 18
    • 0032883420 scopus 로고    scopus 로고
    • Synergistic cytotoxicity and apoptosis by apo-2 ligand and adriamycin against bladder cancer cells
    • Mizutani Y, Yoshida O, Miki T and Bonavida B: Synergistic cytotoxicity and apoptosis by apo-2 ligand and adriamycin against bladder cancer cells. Clin Cancer Res 5: 2605-2612, 1999.
    • (1999) Clin Cancer Res , vol.5 , pp. 2605-2612
    • Mizutani, Y.1    Yoshida, O.2    Miki, T.3    Bonavida, B.4
  • 19
    • 0033210894 scopus 로고    scopus 로고
    • Selectivity of TRAIL-mediated apoptosis of cancer cells and synergy with drugs: The trail to non-toxic cancer therapeutics
    • Bonavida B, Ng CP, Jazirehi A, Schiller G and Mizutani Y: Selectivity of TRAIL-mediated apoptosis of cancer cells and synergy with drugs: the trail to non-toxic cancer therapeutics. Int J Oncol 15: 793-802, 1999.
    • (1999) Int J Oncol , vol.15 , pp. 793-802
    • Bonavida, B.1    Ng, C.P.2    Jazirehi, A.3    Schiller, G.4    Mizutani, Y.5
  • 20
    • 0036138282 scopus 로고    scopus 로고
    • Potentiation of the sensitivity of renal cell carcinoma cells to TRAIL-mediated apoptosis by subtoxic concentrations of 5-fluorouracil
    • Mizutani Y, Nakanishi H, Yoshida O, Fukushima M, Bonavida B and Miki T: Potentiation of the sensitivity of renal cell carcinoma cells to TRAIL-mediated apoptosis by subtoxic concentrations of 5-fluorouracil. Eur J Cancer 38: 167-176, 2002.
    • (2002) Eur J Cancer , vol.38 , pp. 167-176
    • Mizutani, Y.1    Nakanishi, H.2    Yoshida, O.3    Fukushima, M.4    Bonavida, B.5    Miki, T.6
  • 22
    • 0031731668 scopus 로고    scopus 로고
    • Anticancer activity and toxicity of S-1, an oral combination of tegafur and two biochemical modulators, compared with continuous i.v. infusion of 5-fluorouracil
    • Fukushima M, Shimamoto Y, Kato T, Uchida J, Yonekura R, Ohshimo H and Shirasaka T: Anticancer activity and toxicity of S-1, an oral combination of tegafur and two biochemical modulators, compared with continuous i.v. infusion of 5-fluorouracil. Anticancer Drugs 9: 817-823, 1998.
    • (1998) Anticancer Drugs , vol.9 , pp. 817-823
    • Fukushima, M.1    Shimamoto, Y.2    Kato, T.3    Uchida, J.4    Yonekura, R.5    Ohshimo, H.6    Shirasaka, T.7
  • 23
    • 0036024544 scopus 로고    scopus 로고
    • Supriatno, Harada K, Hoque MO, Bando T, Yoshida H and Sato M: Overexpression of p27Kip1 induces growth arrest and apoptosis in an oral cancer cell line. Oral Oncol 38: 730-736, 2002.
    • Supriatno, Harada K, Hoque MO, Bando T, Yoshida H and Sato M: Overexpression of p27Kip1 induces growth arrest and apoptosis in an oral cancer cell line. Oral Oncol 38: 730-736, 2002.
  • 24
    • 0023277545 scopus 로고
    • Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
    • Chomczynski P and Sacchi N: Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 162: 156-159, 1987.
    • (1987) Anal Biochem , vol.162 , pp. 156-159
    • Chomczynski, P.1    Sacchi, N.2
  • 26
    • 16544362735 scopus 로고    scopus 로고
    • Establishment of enzyme-linked immunosorbent assays for thymidylate synthase and dihydropyriminide dehydrogenase in cancer tissues
    • Kurebayashi J, Yamamoto Y, Udagawa K, Okubo S, Fukushima M and Sonoo H: Establishment of enzyme-linked immunosorbent assays for thymidylate synthase and dihydropyriminide dehydrogenase in cancer tissues. Oncol Rep 11: 973-979, 2004.
    • (2004) Oncol Rep , vol.11 , pp. 973-979
    • Kurebayashi, J.1    Yamamoto, Y.2    Udagawa, K.3    Okubo, S.4    Fukushima, M.5    Sonoo, H.6
  • 27
    • 11144303556 scopus 로고    scopus 로고
    • Tumor dihydropyrimidine dehydrogenase expression is a useful marker in adjuvant therapy with oral fluoropyrimidines after curative resection of colorectal cancer
    • Tsuji T, Sawai T, Takeshita H, Nakagoe T, Hidaka S, Yamaguchi H, Yasutake T, Nagayasu T and Tagawa Y: Tumor dihydropyrimidine dehydrogenase expression is a useful marker in adjuvant therapy with oral fluoropyrimidines after curative resection of colorectal cancer. Cancer Chemother Pharmacol 54: 531-536, 2004.
    • (2004) Cancer Chemother Pharmacol , vol.54 , pp. 531-536
    • Tsuji, T.1    Sawai, T.2    Takeshita, H.3    Nakagoe, T.4    Hidaka, S.5    Yamaguchi, H.6    Yasutake, T.7    Nagayasu, T.8    Tagawa, Y.9
  • 28
    • 0003177256 scopus 로고
    • Epidemiology of oral cancer in risk markers of oral disease
    • Johnson NW ed, Cambridge, UK: Cambridge University Press, pp
    • Johnson NW: Epidemiology of oral cancer in risk markers of oral disease. In: Oral Cancer. Johnson NW (ed.). Vol. 2. Cambridge, UK: Cambridge University Press, pp. 3-26, 1991.
    • (1991) Oral Cancer , vol.2 , pp. 3-26
    • Johnson, N.W.1
  • 29
    • 4344564478 scopus 로고
    • Identification of novel genes associated with the response to 5-FU treatment in gastric cancer cell lines using a cDNA microarray
    • Park JS, Young Yoon S, Kim JM, Yeom YI, Kim YS and Kim NS: Identification of novel genes associated with the response to 5-FU treatment in gastric cancer cell lines using a cDNA microarray. Cancer Lett 214: 19-33, 1991.
    • (1991) Cancer Lett , vol.214 , pp. 19-33
    • Park, J.S.1    Young Yoon, S.2    Kim, J.M.3    Yeom, Y.I.4    Kim, Y.S.5    Kim, N.S.6
  • 31
    • 31044445865 scopus 로고    scopus 로고
    • Expression of thymidylate synthase, dihydropyrimidine dehydrogenase, thymidine phosphorylase, and orotate phosphoribosyl transferase in prostate cancer
    • Miyoshi Y, Uemura H, Ishiguro H, Kitamura H, Nomura N, Danenberg PV and Kubota Y: Expression of thymidylate synthase, dihydropyrimidine dehydrogenase, thymidine phosphorylase, and orotate phosphoribosyl transferase in prostate cancer. Prostate Cancer Prostatic Dis 8: 260-265, 2005.
    • (2005) Prostate Cancer Prostatic Dis , vol.8 , pp. 260-265
    • Miyoshi, Y.1    Uemura, H.2    Ishiguro, H.3    Kitamura, H.4    Nomura, N.5    Danenberg, P.V.6    Kubota, Y.7
  • 34
    • 17544367410 scopus 로고    scopus 로고
    • Induction of apoptosis by apo-2 ligand, a new member of the tumor necrosis factor cytokine family
    • Pitti RM, Marsters SA, Ruppert S, Donahue CJ, Moore A and Ashkenazi A: Induction of apoptosis by apo-2 ligand, a new member of the tumor necrosis factor cytokine family. J Biol Chem 271: 12687-12690, 1996.
    • (1996) J Biol Chem , vol.271 , pp. 12687-12690
    • Pitti, R.M.1    Marsters, S.A.2    Ruppert, S.3    Donahue, C.J.4    Moore, A.5    Ashkenazi, A.6


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