| Literature DB >> 29358095 |
Lingfeng He1, Huan Yang2, Shiying Zhou2, Hong Zhu2, Huiwen Mao2, Zhuang Ma2, Ting Wu2, Alagamuthu Karthick Kumar2, Chandrasekhar Kathera2, Avilala Janardhan2, Feiyan Pan2, Zhigang Hu2, Yanhua Yang3, Libo Luo4, Zhigang Guo5.
Abstract
Studies on cervical cancer are urgently required to improve clinical outcomes. As a major anticancer drug for cervical cancer, paclitaxel has been used for many years in clinical therapy but its therapeutic efficacy is limited by common obstacle from cancer cells. The enhanced DNA repair pathways of cancer cells have been proved to survive DNA damage induced by chemotherapeutic drug. Inhibitors of specific DNA repair pathway can sensitize cancer cells to the treatment of chemotherapeutic drugs. In this paper we found that the effect of paclitaxel can be significantly improved when used in combination with FEN1 inhibitor SC13, suggesting a synergistic mechanism between the two compounds. Our studies suggest that FEN1 inhibition could be a novel strategy of tumor-targeting therapy for cervical cancer. Our work also revealed that paclitaxel demonstrates stronger synergistic effect with SC13 than other common used chemical drugs such as doxorubicin, carboplatin or camptothecin on cervical cancer cells.Entities:
Keywords: Cervical cancer; Chemotherapeutic drug; FEN1; Paclitaxel
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Year: 2018 PMID: 29358095 DOI: 10.1016/j.dnarep.2018.01.003
Source DB: PubMed Journal: DNA Repair (Amst) ISSN: 1568-7856