z-logo
open-access-imgOpen Access
GALNT14 regulates ferroptosis and apoptosis of ovarian cancer through the EGFR/mTOR pathway
Author(s) -
Huawen Li,
Mubiao Liu,
Xue Jiang,
Ting Song,
Shuxian Feng,
Jingya Wu,
Pengfei Deng,
Xiaoyu Wang
Publication year - 2022
Publication title -
future oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.857
H-Index - 72
eISSN - 1744-8301
pISSN - 1479-6694
DOI - 10.2217/fon-2021-0883
Subject(s) - downregulation and upregulation , ovarian cancer , pi3k/akt/mtor pathway , cisplatin , cancer research , apoptosis , medicine , blot , cancer , oncology , chemotherapy , biology , biochemistry , gene
Background: Chemoresistance usually occurs in ovarian cancer. We aimed to explore the mechanisms of chemoresistance. Methods: Western blotting assay was used to detect the expression of GALNT14. Further cell function experiments were performed to investigate the effect of GALNT14 in ovarian cancer. Results: GALNT14 is significantly upregulated in ovarian cancer. Downregulation of GALNT14 significantly inhibits both apoptosis and ferroptosis of ovarian cancer cells. A further mechanism assay illustrated that downregulation of GALNT14 suppresses the activity of the mTOR pathway through modifying O-glycosylation of EGFR. Finally, an additive effect promoting cell death occurs with a combination of an mTOR inhibitor and cisplatin. Conclusion: Our study might provide a promising method to overcome cisplatin resistance for patients with ovarian cancer.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here