TTYH3 Modulates Bladder Cancer Proliferation and Metastasis via FGFR1/H-Ras/A-Raf/MEK/ERK Pathway

التفاصيل البيبلوغرافية
العنوان: TTYH3 Modulates Bladder Cancer Proliferation and Metastasis via FGFR1/H-Ras/A-Raf/MEK/ERK Pathway
المؤلفون: Polash Kumar Biswas, Yeonjoo Kwak, Aram Kim, Jaekwon Seok, Hee Jeong Kwak, Moonjung Lee, Ahmed Abdal Dayem, Kwonwoo Song, Jae-Yong Park, Kyoung Sik Park, Hyun Jin Shin, Ssang-Goo Cho
المصدر: International Journal of Molecular Sciences; Volume 23; Issue 18; Pages: 10496
سنة النشر: 2022
مصطلحات موضوعية: Mitogen-Activated Protein Kinase Kinases, MAP Kinase Signaling System, Organic Chemistry, General Medicine, Catalysis, Computer Science Applications, Inorganic Chemistry, Urinary Bladder Neoplasms, Chloride Channels, Cell Line, Tumor, Humans, bladder cancer, FGFR1, gene expression, MAPK, patient survival, TTYH3, RNA, Messenger, Receptor, Fibroblast Growth Factor, Type 1, Physical and Theoretical Chemistry, Molecular Biology, Spectroscopy, Cell Proliferation
الوصف: Tweety family member 3 (TTYH3) is a calcium-activated chloride channel with a non-pore-forming structure that controls cell volume and signal transduction. We investigated the role of TTYH3 as a cancer-promoting factor in bladder cancer. The mRNA expression of TTYH3 in bladder cancer patients was investigated using various bioinformatics databases. The results demonstrated that the increasingly greater expression of TTYH3 increasingly worsened the prognosis of patients with bladder cancer. TTYH3 knockdown bladder cancer cell lines were constructed by their various cancer properties measured. TTYH3 knockdown significantly reduced cell proliferation and sphere formation. Cell migration and invasion were also significantly reduced in knockdown bladder cancer cells, compared to normal bladder cancer cells. The knockdown of TTYH3 led to the downregulation of H-Ras/A-Raf/MEK/ERK signaling by inhibiting fibroblast growth factor receptor 1 (FGFR1) phosphorylation. This signaling pathway also attenuated the expression of c-Jun and c-Fos. The findings implicate TTYH3 as a potential factor regulating the properties of bladder cancer and as a therapeutic target.
وصف الملف: application/pdf
تدمد: 1422-0067
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd6ddd120249366d0eced2b8c61e57f9Test
https://pubmed.ncbi.nlm.nih.gov/36142409Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....dd6ddd120249366d0eced2b8c61e57f9
قاعدة البيانات: OpenAIRE