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Growth inhibition and radiosensitivity enhancement of lung cancer cell line by a selective cyclooxygenase-2 inhibitor

Shaoying Ma

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Abstract

Objective To investigate the growth,apoptosis and ra diosensitivity enhancement of lung cancer cell line A549 by a selective cyclooxy genase-2 inhibitor,celecoxib. Methods The effect of celecoxib on the survival of A549 tumor cells was measured by MTT, the cell cycle and apop tosis were measured using flow cytometric method(FCM). Radiosensitivity effect o f celecoxib on A549 cells was assayed by clonal survival. Results The inhibitory rate of 50μmol/L celecoxib dealing with A549 tumor cells in 24 and 72 hours were 4.27±1.33(%) and 10.63±2.23(%) respectively, 100μmol/ L were 33.47±8.02(%), 61.97±7.32(%),respectively. This effect was mainly in hibiting proliferation, leading to arrest of cells in G0/G1 phase and cell death when 100μmol/L dealing in 72 hours. Celecoxib did not induce any apoptosis i n A549 tumor cells or render tumor cells more susceptible to radiation-induced apoptosis. The cell clonal survival assay showed that celecoxib decreased the ca lculated survival fraction (SF) for all radiation doses, especially in high dose s. The survival fractions in 2 Gy radiation dose in contrast and dealing with 10 0μmol/L celecoxib 24 and 72 hours were 0.53±0.06, 0.52±0.11 and 0.46±0.05 ,respectively; The radiation enhancement ratios in dealing 24 and 72 hours were 1.27 and 1.7(a ratio of D 0 value),respectively. Conclusion C elecoxib siginificently inhibited the growth and proliferation of A549 tumor cel ls, this effect is time and dose dependent, leading to accumulation of tumor cel ls in G 0/G 1 phase; but can not induced apoptosis. Celecoxib enhances radiose nsitivity of A549 tumor cells and is time and the dose dependent. This effect is more efficient in high radiation dose.

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Objective To investigate the growth,apoptosis and ra diosensitivity enhancement of lung cancer cell line A549 by a selective cyclooxy genase-2 inhibitor,celecoxib. Methods The effect of celecoxib on the survival of A549 tumor cells was measured by MTT, the cell cycle and apop tosis were measured using flow cytometric method(FCM). Radiosensitivity effect o f celecoxib on A549 cells was assayed by clonal survival. Results The inhibitory rate of 50μmol/L celecoxib dealing with A549 tumor cells in 24 and 72 hours were 4.27±1.33(%) and 10.63±2.23(%) respectively, 100μmol/ L were 33.47±8.02(%), 61.97±7.32(%),respectively. This effect was mainly in hibiting proliferation, leading to arrest of cells in G0/G1 phase and cell death when 100μmol/L dealing in 72 hours. Celecoxib did not induce any apoptosis i n A549 tumor cells or render tumor cells more susceptible to radiation-induced apoptosis. The cell clonal survival assay showed that celecoxib decreased the ca lculated survival fraction (SF) for all radiation doses, especially in high dose s. The survival fractions in 2 Gy radiation dose in contrast and dealing with 10 0μmol/L celecoxib 24 and 72 hours were 0.53±0.06, 0.52±0.11 and 0.46±0.05 ,respectively; The radiation enhancement ratios in dealing 24 and 72 hours were 1.27 and 1.7(a ratio of D 0 value),respectively. Conclusion C elecoxib siginificently inhibited the growth and proliferation of A549 tumor cel ls, this effect is time and dose dependent, leading to accumulation of tumor cel ls in G 0/G 1 phase; but can not induced apoptosis. Celecoxib enhances radiose nsitivity of A549 tumor cells and is time and the dose dependent. This effect is more efficient in high radiation dose.

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Available abstract

Objective To investigate the growth,apoptosis and ra diosensitivity enhancement of lung cancer cell line A549 by a selective cyclooxy genase-2 inhibitor,celecoxib. Methods The effect of celecoxib on the survival of A549 tumor cells was measured by MTT, the cell cycle and apop tosis were measured using flow cytometric method(FCM). Radiosensitivity effect o f celecoxib on A549 cells was assayed by clonal survival. Results The inhibitory rate of 50μmol/L celecoxib dealing with A549 tumor cells in 24 and 72 hours were 4.27±1.33(%) and 10.63±2.23(%) respectively, 100μmol/ L were 33.47±8.02(%), 61.97±7.32(%),respectively. This effect was mainly in hibiting proliferation, leading to arrest of cells in G0/G1 phase and cell death when 100μmol/L dealing in 72 hours. Celecoxib did not induce any apoptosis i n A549 tumor cells or render tumor cells more susceptible to radiation-induced apoptosis. The cell clonal survival assay showed that celecoxib decreased the ca lculated survival fraction (SF) for all radiation doses, especially in high dose s. The survival fractions in 2 Gy radiation dose in contrast and dealing with 10 0μmol/L celecoxib 24 and 72 hours were 0.53±0.06, 0.52±0.11 and 0.46±0.05 ,respectively; The radiation enhancement ratios in dealing 24 and 72 hours were 1.27 and 1.7(a ratio of D 0 value),respectively. Conclusion C elecoxib siginificently inhibited the growth and proliferation of A549 tumor cel ls, this effect is time and dose dependent, leading to accumulation of tumor cel ls in G 0/G 1 phase; but can not induced apoptosis. Celecoxib enhances radiose nsitivity of A549 tumor cells and is time and the dose dependent. This effect is more efficient in high radiation dose.

Key concepts: Celecoxib, Radiosensitivity, A549 cell, Apoptosis, Cell cycle, Cell growth, Growth inhibition, Lung cancer

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