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Table 5 Significant (p < 0.01) inhibitors, their potential target kinases and phosphatases and their effects on VSMC proliferation

From: Gene expression profiles and signaling mechanisms in α2B-adrenoceptor-evoked proliferation of vascular smooth muscle cells

Inhibitor

Inhibition of proliferation

[% of control]

Potential target kinases and phosphatases

Effect of target kinase/phosphatase on VSMC proliferation

Reference

Fenvalerate

32

calcineurin

[61, 173,174,175]

5,6-dichloro-1-beta-D-ribofuranosyl benzimidazole

31

CK2

[176, 192, 303,304,305]

Cdk9

[306, 307]

PP2

31

Src family kinases

[177,178,179,180,181,182, 308]

PP1

18

SP600125

30

JNKs

[183, 184]

SB-202190

30

p38 MAPKs

[185,186,187]

Olomoucine

29

Cdk1, Cdk2

[85, 188,189,190,191]

Benzylphosphonic acid

27

tyrosine phosphatases

↑/↓

[309,310,311]

L-p-bromotetramisole

25

alkaline phosphatase

n.d.

[312, 313]

tyrosine phosphatases

↑/↓

[309,310,311]

LFM-A13

24

BTK, Plk, Jak2

[314,315,316,317]

Daidzein

24

arrests cell cycle at G1

[318,319,320]

LY294002

23

PI3-kinases

[173, 180, 192,193,194,195]

Tyrphostin AG 1478

21

EGFR

[179, 196,197,198,199]

2-Aminopurine

17

PKR

[321, 322]

GW5074

16

Raf-1

[37, 177, 200]

  1. CK2 = protein kinase CK2 (casein kinase), Cdks 1,2 and 9 = cyclin-dependent kinases 1,2 and 9, Src family kinases = Src, Fyn, Hck and Lck, JNKs = c-Jun N-terminal kinases, p38 MAPKs = p38 mitogen-activated protein kinases, BTK = Bruton’s tyrosine kinase, Plk = Polo-like kinase, Jak2 = Janus kinase 2, PI3 kinase = phosphoinositide 3-kinase, EGFR = epidermal growth factor receptor, PKR = ds-RNA-activated protein kinase, Raf-1 = RAF proto-oncogene serine/threonine-protein kinase. In cases when little data are available in VSMCs, the table was augmented with information of kinase/phosphatase effects on cell proliferation in other cell types