MARVELD1 interacting with catalase regulates reactive oxygen species metabolism and mediates the sensitivity to chemotherapeutic drugs in epithelial tumors of the reproductive system

التفاصيل البيبلوغرافية
العنوان: MARVELD1 interacting with catalase regulates reactive oxygen species metabolism and mediates the sensitivity to chemotherapeutic drugs in epithelial tumors of the reproductive system
المؤلفون: Ming Shi, Yuanfei Yao, Jie He, Haoxiu Sun, Muhammad Luqman Akhtar, Yiqun Li, Fang Han, Huan Nie, Yanpeng Ci, Yu Li, Chunbin Zhang, Peng Dou
المصدر: Molecular carcinogenesis. 58(8)
سنة النشر: 2019
مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Mice, Nude, Biology, Mitochondrion, 03 medical and health sciences, Mice, 0302 clinical medicine, Cell Line, Tumor, Carcinoma, medicine, Animals, Humans, Reproductive system, Neoplasms, Glandular and Epithelial, RNA, Small Interfering, Molecular Biology, Cell Proliferation, chemistry.chemical_classification, Reactive oxygen species, Mice, Inbred BALB C, Membrane Proteins, Metabolism, Cell cycle, medicine.disease, Catalase, Cell biology, Mice, Inbred C57BL, Oxidative Stress, 030104 developmental biology, chemistry, Cytoplasm, 030220 oncology & carcinogenesis, biology.protein, Female, RNA Interference, Reactive Oxygen Species, Microtubule-Associated Proteins, HeLa Cells
الوصف: Previous investigations have found that MARVEL domain-containing 1 (MARVELD1) could inhibit tumor cell proliferation and enhance the sensitivity to chemotherapeutic drugs in hepatocellular carcinoma. Hence, it may be a valuable therapeutic target. In the study, we analyzed the responsive changes of MARVELD1 to 25 stress factors and expression of MARVELD1 in epithelial tumors of the reproductive system. We found that MARVELD1 was transferred to the cytoplasm and mitochondria under cell stress. And under cellular stress, the reactive oxygen species (ROS) levels decreased in MARVELD1 expressed cells while increased in the cells of MARVELD1-specific siRNA treatment. Meanwhile, MARVELD1 overexpression significantly promoted the inhibition of tumor cell proliferation under cellular stress via affecting ROS metabolism, not cell cycle. In xenograft tumor tissues with MARVELD1 expression, the tumor growth was inhibited and accompanied by the lower ROS levels. Furthermore, we identified that MARVELD1 could interact with catalase (CAT) to enhance latter activity and maintain stability. And the enhanced sensitivity to chemotherapeutic drugs clearly depended on the ability of MARVELD1 scavenge the ROS in carcinoma cells of the reproductive system. Our findings clearly explain that MARVELD1 may regulate tumor cell proliferation and sensitivity to chemotherapeutic drugs via reducing the exorbitant ROS. The mechanism was that MARVELD1 interacted with CAT to maintain latter stability, and then ensure continuous ROS scavenge.
تدمد: 1098-2744
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c159d2b24788741e0917e6baeb622f9
https://pubmed.ncbi.nlm.nih.gov/31066116
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....4c159d2b24788741e0917e6baeb622f9
قاعدة البيانات: OpenAIRE