RSM-932A is a ChoKα inhibitor with potent in vitro antiproliferative activity against a large variety of tumor-derived cell lines and in vivo antitumoral activity against human xenographs in mice. RSM-932A also shows high efficacy with low toxicity at the effective doses.[1]
In vitro experiments indicated that RSM-932A has a potent antiproliferative activity against most tumor-derived cell lines tested, including those derived from breast, lung, colon, bladder, liver, ovary, bone, cervix, kidney, pancreas, melanoma and brain tumors, with IC50 (1.15 ± 0.14 μM) in the low, single-digit micromolar range, consistent with a cytotoxic effect.
|
RSM-932A (72 h) |
|||||||||
|
Type of tumor |
Cell line |
IC50 |
±SD |
GI50 |
±SD |
TGI |
±SD |
LC50 |
±SD |
|
Breast |
MDA-MB-231 |
1.3 |
0.5 |
1.2 |
0.2 |
2.0 |
0.1 |
2.7 |
1.2 |
|
T47D |
2,2 |
0,9 |
1,3 |
0,8 |
NA |
NA |
>6 |
NA |
|
|
MDA.MB.468 |
2.4 |
1.0 |
1.6 |
0.4 |
3.1 |
1.6 |
>6 |
0.5 |
|
|
SkBr-3 |
3.1 |
0.6 |
1.0 |
0.6 |
1.6 |
0.5 |
13.2 |
6.7 |
|
|
Lung |
H510 |
1.4 |
0.3 |
1.0 |
NA |
1.1 |
0.5 |
3.9 |
1.8 |
|
H1299 |
1.9 |
0.1 |
1.0 |
0.0 |
1.9 |
0.7 |
7.4 |
3.0 |
|
|
H460 |
1.9 |
0.5 |
1.0 |
0.0 |
1.7 |
0.6 |
5.2 |
1.3 |
|
|
Colon |
HT-29 |
1.7 |
0.4 |
1.3 |
0.2 |
5.6 |
6.6 |
11.0 |
5.4 |
|
HCT-116 |
1.8 |
0.3 |
1.0 |
0.3 |
1.7 |
1.0 |
>6 |
NA |
|
|
DLD-1 |
2.1 |
0.7 |
1.6 |
0.5 |
3.3 |
0.9 |
6.3 |
2.8 |
|
|
SW620 |
2.1 |
0.7 |
1.6 |
0.5 |
3.3 |
0.9 |
6.3 |
2.8 |
|
|
Bladder |
HT-1376 |
1.5 |
0.3 |
1.0 |
0.0 |
5.7 |
1.2 |
>6.5 |
NA |
|
TccSup |
1.6 |
0.2 |
1.1 |
0.5 |
1.5 |
0.0 |
>6.5 |
NA |
|
|
SW780 |
1.6 |
0.4 |
1.4 |
0.3 |
2.3 |
0.5 |
8.2 |
3.1 |
|
|
J82 |
2.3 |
1.3 |
1.6 |
1.2 |
NA |
NA |
5.0 |
2.1 |
|
|
Epithelial carcinoma |
A431 |
2.2 |
0.1 |
1.5 |
0.5 |
NA |
NA |
3.5 |
0.7 |
|
Liver |
Hep3B2 |
2.4 |
0.5 |
1.2 |
0.1 |
2.7 |
1.4 |
3.2 |
0.8 |
|
HepG2 |
6.4 |
2.2 |
1.3 |
0.3 |
8.4 |
1.3 |
>12 |
NA |
|
|
Ovary |
OV-Car-3 |
3.4 |
0.3 |
1.7 |
0.2 |
2.9 |
0.4 |
5.5 |
0.5 |
|
SK-OV-3 |
6.4 |
2.2 |
1.3 |
0.3 |
8.4 |
1.3 |
>12 |
NA |
|
|
Bone |
SAOS-2 |
1.3 |
0.1 |
<1.6 |
NA |
2.2 |
0.7 |
5.1 |
1.5 |
|
Cervix |
HeLa |
1.7 |
0.7 |
1.0 |
NA |
1.5 |
0.0 |
5.7 |
1.2 |
|
Kidney |
769-P |
1.4 |
0.2 |
1.0 |
0.4 |
2.4 |
1.2 |
>3.5 |
0.7 |
|
Melanoma |
SKMel-28 |
1.3 |
0.3 |
0.5 |
0.0 |
0.4 |
0.1 |
1.5 |
0.4 |
|
A-375 |
6.2 |
1.9 |
2.6 |
1.4 |
5.6 |
1.1 |
7.7 |
1.4 |
|
|
Pancreas |
Mia.PaCa.2 |
2.3 |
0.2 |
1.7 |
0.3 |
3.5 |
0.4 |
5.5 |
1.4 |
|
Astrocytoma, gliocystoma |
U-87 |
1.9 |
0.5 |
1.4 |
0.2 |
5.0 |
1.2 |
8.9 |
4.3 |
|
Control |
MCF10-A |
7.1 |
0.5 |
3.4 |
0.8 |
7.2 |
1.3 |
14.7 |
1.3 |
Table 1.Panel of human cancer cell lines tested with RSM-932A for 72 hours and determination of IC50, GI50, TGI, and LC50 parameters
In vivo experiments demonstrated that RSM-932A shows no detectable toxicity in mice at highly effective doses with 77% tumor growth inhibition.[1]
References:
[1]. Lacal JC, et al. Preclinical characterization of RSM-932A, a novel anticancer drug targeting the human choline kinase alpha, an enzyme involved in increased lipid metabolism of cancer cells. Mol Cancer Ther. 2015 Jan;14(1):31-9.
\n\n\n\n\n\n
\n
RSM-932A 是一种 ChoKα 抑制剂,对多种肿瘤来源的细胞系具有有效的体外抗增殖活性,对小鼠的人异种移植物具有体内抗肿瘤活性。 RSM-932A 在有效剂量下也表现出高效低毒。[1]
体外实验表明,RSM-932A 对测试的大多数肿瘤衍生细胞系具有有效的抗增殖活性,包括来自乳腺、肺、结肠、膀胱、肝脏、卵巢、骨骼、子宫颈、肾脏、胰腺、黑色素瘤的细胞系和脑肿瘤,IC50 (1.15 ± 0.14 μM) 在低个位数微摩尔范围内,与细胞毒性作用一致。
\n<表格样式=\
















