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. 2016 Mar 2;7(12):14841–14856. doi: 10.18632/oncotarget.7854

Table 1. List of compounds used in this study.

Drugs* Target IC50**
Taxol Microtubule Stabilizing 10 nM
Nocadazole Microtubule Destabilizing 5 μM
SAHA Histone Deacetylase 2 μM
Romidepsin Histone Deacetylase 2 nM
Olaparib Poly ADP Ribose Polymerase 10 μM
LMP400 Topoisomerase I 50 nM
Gemcitabine Ribonucleotide Reductase 50 nM
PF-2771 CENP-E 10 μM
GSK923295*** CENP-E 10 μM
Zoledronic acid CENP-F 10 μM
siRNA target Sense sequence as ordered**** siRNA per well
(6-well plate)
SKA3 5′-AGACAAACAUGAACAUUAAUU-3′ 25 pmol
CENP-E 5′-AACACGGAUGCUGGUGACCUC-3′ 25 pmol
MIS18β 5′-AGGCAGUACUUACAACCUUUU-3′ 25 pmol
ON-TAGET plus, Non-targeting pool 5′-UGGUUUACAUGUCGACUAA-3′
5′-UGGUUUACAUGUUGUGUGA-3′
5′-UGGUUUACAUGUUUUCUGA-3′
5′-UGGUUUACAUGUUUUCCUA-3′
25 pmol
*

All drugs, except RF-1771, GSK92395 and zoledronic acid, were described in our previous publications [15, 25]. GSK92395 was purchased from Selleckchem (Catalog no. S7090). PF-1771 was kindly provided by Dr. B.W. Murray (Pfizer Worldwide Research and Development, La Jolla Laboratories, San Diego). Zoledronic acid was purchased from Novartis Pharma AG (Stein, Switzerland).

**

The cells were treated overnight.

***

For HT1080 cells containing EGFP-HAC, IC50 for GSK923295 was 2 μM. For HT1080 cells containing mCherry-shRNA-HAC, IC50 was 10 μM.

****

The two underlined uracil (UU) were added by Dharmacon as part of siRNA construction.