Inhibition of COX2 enhances the chemosensitivity of dichloroacetate in cervical cancer cells
Dichloroacetate (DCA), a traditional mitochondria-targeting agent, has shown promising prospect as a sensitizer in fighting against malignancies including cervical cancer. But it is unclear about the effect of DCA alone on cervical tumor. Moreover, previous reports have demonstrated that the increased cyclooxygenase-2 (COX2) expression is associated with chemoresistance and poor prognosis of cervical cancer. However, it is still unknown whether COX2 can affect the sensitivity of DCA in cervical cancer cells. In this study, we found that cervical cancer cells were insensitive to DCA. Furthermore, we for the first time revealed that DCA could upregulate COX2 which impeded the chemosensitivity of DCA in cervical cancer cells. Mechanistic study showed that DCA reduced the level of RNA binding protein quaking (QKI), leading to the decay suppression of COX2 mRNA and the subsequent elevation of COX2 protein. Inhibition of COX2 using celecoxib could sensitize DCA in repressing the growth of cervical cancer cells both in vitro and in vivo. These results indicate that COX2 is a novel resistance factor of DCA, and combination of celecoxib with DCA may be beneficial to the treatment of cervical cancer.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2017 |
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| Erschienen: |
2017 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:8 |
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| Enthalten in: |
Oncotarget - 8(2017), 31 vom: 01. Aug., Seite 51748-51757 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Li, Bo [VerfasserIn] |
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| Links: |
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| Themen: |
COX2 |
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| Anmerkungen: |
Date Completed 25.09.2017 Date Revised 13.11.2018 published: Electronic-eCollection Citation Status PubMed-not-MEDLINE |
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| doi: |
10.18632/oncotarget.18518 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM275531376 |
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| 520 | |a Dichloroacetate (DCA), a traditional mitochondria-targeting agent, has shown promising prospect as a sensitizer in fighting against malignancies including cervical cancer. But it is unclear about the effect of DCA alone on cervical tumor. Moreover, previous reports have demonstrated that the increased cyclooxygenase-2 (COX2) expression is associated with chemoresistance and poor prognosis of cervical cancer. However, it is still unknown whether COX2 can affect the sensitivity of DCA in cervical cancer cells. In this study, we found that cervical cancer cells were insensitive to DCA. Furthermore, we for the first time revealed that DCA could upregulate COX2 which impeded the chemosensitivity of DCA in cervical cancer cells. Mechanistic study showed that DCA reduced the level of RNA binding protein quaking (QKI), leading to the decay suppression of COX2 mRNA and the subsequent elevation of COX2 protein. Inhibition of COX2 using celecoxib could sensitize DCA in repressing the growth of cervical cancer cells both in vitro and in vivo. These results indicate that COX2 is a novel resistance factor of DCA, and combination of celecoxib with DCA may be beneficial to the treatment of cervical cancer | ||
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| 650 | 4 | |a QKI | |
| 650 | 4 | |a celecoxib | |
| 650 | 4 | |a cervical cancer | |
| 650 | 4 | |a dichloroacetate | |
| 700 | 1 | |a Li, Xinzhe |e verfasserin |4 aut | |
| 700 | 1 | |a Xiong, Haojun |e verfasserin |4 aut | |
| 700 | 1 | |a Zhou, Peng |e verfasserin |4 aut | |
| 700 | 1 | |a Ni, Zhenhong |e verfasserin |4 aut | |
| 700 | 1 | |a Yang, Teng |e verfasserin |4 aut | |
| 700 | 1 | |a Zhang, Yan |e verfasserin |4 aut | |
| 700 | 1 | |a Zeng, Yijun |e verfasserin |4 aut | |
| 700 | 1 | |a He, Jintao |e verfasserin |4 aut | |
| 700 | 1 | |a Yang, Fan |e verfasserin |4 aut | |
| 700 | 1 | |a Zhang, Nan |e verfasserin |4 aut | |
| 700 | 1 | |a Wang, Yuting |e verfasserin |4 aut | |
| 700 | 1 | |a Zheng, Yingru |e verfasserin |4 aut | |
| 700 | 1 | |a He, Fengtian |e verfasserin |4 aut | |
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