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. 2005 Mar 29;92(8):1486–1492. doi: 10.1038/sj.bjc.6602498

Table 1. IC50 against MX2 and etoposide, adriamycin, and vincristine with or without indomethacin, 5-Aza-2′-deoxycytidine (5AZ) treatment.

  MX2 (nM) Etoposide (nM) Adriamycin (nM) Vincristine (nM) Carboplatin (μM)
K562/P 30±4 10±4 20±3 2.0±2.1 20±5.1
K562/P with indomethacin 28±7 9±5 18±3 1.8±2.0 ND
K562/P with 2 μM 5AZ 28±5 8±5 ND ND ND
K562/P with 10 μM 5AZ 29±6 7±4 15.0±11.0 1.8±2.9 22±4.8
K562/MX2 200±23* 94±15* 150±20* 2.3±1.8 18±6.0
K562/MX2 with indomethacin 190±50* 90±25* 100±25* 1.8±1.0 ND
K562/MX2 with 2 μM 5AZ 50±12a 10±5a ND ND ND
K562/MX2 with 10 μM 5AZ 46±9a 8±5a 130±10.7 2.0±1.0 20.5±4.8
K562/ADM 28±9.3 8.2±3.0 250±50* 20.2±8.1* 21±6.8
K562/ADM with indomethacin ND ND 50±50** 5±3** ND
K562/ADM with 10 μM 5AZ 30±8.8 9.3±2.5 100±20.8a 5.0±2.8a 20±5.0

ND=not done. IC50 was calculated from cytotoxicity against various drugs. Data were average±s.d. from five independent experiments.

*

P<0.05, cytotoxicity in K562/P vs K562/MX2, or K562/ADM cells.

**

P<0.05, cytotoxicity in K562 cells with vs without indomethacin treatment.

a

Cytotoxicity in K562 cells with vs without 5AZ treatment.