IL-1α
|
Proinflammatory |
(i) Stimulate angiogenesis |
(i) In vitro/In vivo
|
[27] |
(ii) Recruit immunocompetent cells |
(ii) In vitro/In vivo
|
[28–33] |
(iii) Increase platelet count |
(iii) Phase I clinical trial |
[34, 35] |
|
IL-1β
|
Proinflammatory |
(i) Increase expression of MMP-1 |
(i) In vitro
|
[36] |
(ii) Stimulate production of proangiogenic factors |
(ii) In vitro
|
[37] |
(iii) Promote OC cell migration and invasion |
(iii) In vitro
|
[38] |
|
IL-1Ra |
Anti-inflammatory |
(i) Antagonist to IL-1α and IL-1β
|
|
[39] |
(ii) Abundant in the OC ascites |
In vivo
|
[31, 40] |
|
IL-6 |
Anti-inflammatory |
(i) Promote OC cell proliferation |
(i) In vitro
|
[41] |
(ii) Stimulate angiogenesis |
(ii) In vitro/In vivo
|
[42] |
(iii) Enhance endothelial cell migration |
(iii) In vitro/In vivo
|
[42] |
(iv) Increase OC cell lines capacity to secrete MMP-9 |
(iv) In vitro
|
[43] |
(v) Increase chemotactic and/or chemokinetic activity |
(v) In vitro
|
[44] |
(vi) Increase invasiveness |
(vi) In vitro
|
[44] |
(vii) Induce chemoresistance |
(vii) In vitro/In vivo
|
[45–47] |
(viii) Increase platelet count |
(viii) Phase I and II clinical trial |
[48, 49] |