دورية أكاديمية

Transcriptomics analysis revealed that TAZ regulates the proliferation of KIRC cells through mitophagy

التفاصيل البيبلوغرافية
العنوان: Transcriptomics analysis revealed that TAZ regulates the proliferation of KIRC cells through mitophagy
المؤلفون: Zhen He, Jianxi Shi, Bing Zhu, Zhentao Tian, Zhihong Zhang
المصدر: BMC Cancer, Vol 24, Iss 1, Pp 1-12 (2024)
بيانات النشر: BMC, 2024.
سنة النشر: 2024
المجموعة: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
مصطلحات موضوعية: Renal clear cell carcinoma (KIRC), Transcriptional co-activator with PDZ-Binding motif (TAZ), The Cancer Genome Atlas (TCGA), Mitophagy, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: Abstract Transcriptional Co-Activator with PDZ-Binding Motif (TAZ, also known as WWTR1) is a downstream effector of the Hippo pathway, involved in the regulation of organ regeneration and cell differentiation in processes such as development and regeneration. TAZ has been shown to play a tumor-promoting role in various cancers. Currently, many studies focus on the role of TAZ in the process of mitophagy. However, the molecular mechanism and biological function of TAZ in renal clear cell carcinoma (KIRC) are still unclear. Therefore, we systematically analyzed the mRNA expression profile and clinical data of KIRC in The Cancer Genome Atlas (TCGA) dataset. We found that TAZ expression was significantly upregulated in KIRC compared with normal kidney tissue and was closely associated with poor prognosis of patients. Combined with the joint analysis of 36 mitophagy genes, it was found that TAZ was significantly negatively correlated with the positive regulators of mitophagy. Finally, our results confirmed that high expression of TAZ in KIRC inhibits mitophagy and promotes KIRC cell proliferation. In conclusion, our findings reveal the important role of TAZ in KIRC and have the potential to be a new target for KIRC therapy.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1471-2407
Relation: https://doaj.org/toc/1471-2407
DOI: 10.1186/s12885-024-11903-9
URL الوصول: https://doaj.org/article/439128132300406d97659f1a341efa5d
رقم الأكسشن: edsdoj.439128132300406d97659f1a341efa5d
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14712407
DOI:10.1186/s12885-024-11903-9