RRC ID 18747
著者 Egawa-Takata T, Endo H, Fujita M, Ueda Y, Miyatake T, Okuyama H, Yoshino K, Kamiura S, Enomoto T, Kimura T, Inoue M.
タイトル Early reduction of glucose uptake after cisplatin treatment is a marker of cisplatin sensitivity in ovarian cancer.
ジャーナル Cancer Sci
Abstract Cisplatin is an effective chemotherapeutic agent for ovarian cancer, but the sensitivity of cancers differs in individual cases. Because cisplatin is reported to suppress glucose uptake, we investigated the correlation between glucose uptake and sensitivity to the drug. A fluorescent derivative of D-glucose, 2-NBDG (2-[N-(7-nitrobenz-2-oxa-1,3-diaxol-4-yl) amino]-2-deoxyglucose), was used to evaluate glucose uptake. Two ovarian cancer cell lines, SKOV-3 as a relatively resistant line and OVCAR-3 as a relatively sensitive line, were analyzed. Both cell lines had a decreased number of cells accompanied by cell death 24 h after cisplatin treatment, but not at 3 h. In contrast, glucose uptake was decreased 3 h after high-dose cisplatin treatment, which correlated with the sensitivity to the drug at 24 h. The protein levels of glucose transporter 1 (GLUT1) did not change with cisplatin treatment. In contrast, the membrane localization of GLUT1 disappeared after cisplatin treatment. Other cisplatin-resistant cell lines did not show an early decrease in glucose uptake after cisplatin treatment. The early decrease in glucose uptake and later cell death also correlated in cultured cancer cells from ovarian cancer patients. Thus, the decrease in glucose uptake at an early time point after high dose cisplatin treatment reflected cisplatin chemosensitivity in ovarian cancer cells. Measuring glucose uptake might be useful as a rapid evaluation of cisplatin chemosensitivity in ovarian cancer patients.
巻・号 101(10)
ページ 2171-8
公開日 2010-10-1
DOI 10.1111/j.1349-7006.2010.01670.x
PII CAS1670
PMID 20678156
MeSH Antineoplastic Agents / pharmacology* Apoptosis / drug effects Cell Line, Tumor Cell Survival / drug effects Cisplatin / pharmacology* Female Glucose / metabolism* Glucose Transporter Type 1 / analysis Humans Membrane Potential, Mitochondrial / drug effects Ovarian Neoplasms / drug therapy* Ovarian Neoplasms / metabolism Ovarian Neoplasms / pathology Oxygen Consumption / drug effects
IF 4.966
引用数 35
WOS 分野 ONCOLOGY
リソース情報
ヒト・動物細胞 NIH:OVCAR-3(RCB2135) Sawano(RCB1152)