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. 2019 Jan 14;11(1):90. doi: 10.3390/cancers11010090

Table 1.

FoxO role in cell sensitivity and resistance to conventional agents.

Tumor Drug Mechanism of Response Ref
Ovarian carcinoma paclitaxel Increased levels and transcriptional activity of FoxO1. Resistance [62]
Ovarian carcinoma cisplatin combined with selinexor Enrichment of FoxO1 nuclear localization. Sensitivity [63]
Ovarian carcinoma cisplatin Down-regulation of FoxO1 levels. Resistance [64]
Colon carcinoma cisplatin FoxO3 dephosphorylation (threonine 32) and nuclear translocation. Sensitivity [65]
Colangiocarcinoma cisplatin Increased transcriptional activity of FoxO3 (up-regulation of Keap1) and activation of proteasome pathway. Sensitivity [66]
Esophageal squamous cell carcinoma cisplatin, paclitaxel FoxO1 stimulation of TGF-β1 expression. Resistance [67]
Hepatocellular carcinoma cisplatin, doxorubicin Suppression of FoxO1 activity (down-regulation of the pro-apoptotic Bim). Resistance [68]
Breast cancer doxorubicin FoxO1 reduced levels and nuclear localization. Resistance [69]
Breast cancer doxorubicin FoxO1 over-expression (up-regulation of ABCB1). Resistance [70]
Leukemic cells doxorubicin FoxO3 activation (stimulation of ABCB1 expression). Resistance [71]
Neuroblastoma doxorubicin and etoposide FoxO3-mediated reduction of survivin expression. Sensitivity [72]
Nasopharyngeal carcinoma 5-fluorouracil miR-3188-mTOR-p-PI3K/AKT-c-JUN feedback loop modulated by FoxO1 sensitize cells. Sensitivity [73]
Colon carcinoma 5-fluorouracil FoxO3 nuclear translocation (down-regulation BAK, BIM, KIP). Resistance [74]