التفاصيل البيبلوغرافية
| العنوان: |
Induction of the RNA regulator LIN28A is required for the growth and pathogenesis of RESTless breast tumors |
| المؤلفون: |
Wyatt B. Potter, Soyoung Kim, Matthew P. Wagoner, Kassondra Meyer, Kearney T. W. Gunsalus, Barry Schoenike, Caroline M. Alexander, Avtar Roopra, Andreas Friedl |
| المصدر: |
Cancer research. 72(13) |
| سنة النشر: |
2012 |
| مصطلحات موضوعية: |
Cancer Research, Chromatin Immunoprecipitation, Blotting, Western, Fluorescent Antibody Technique, Breast Neoplasms, RE1-silencing transcription factor, Biology, Real-Time Polymerase Chain Reaction, Article, Pathogenesis, Mice, Downregulation and upregulation, In vivo, Cell Line, Tumor, medicine, Animals, Humans, Lymph node, Transcription factor, Rest (music), RNA-Binding Proteins, DNA-Binding Proteins, Repressor Proteins, medicine.anatomical_structure, Oncology, Gene Knockdown Techniques, Immunology, Cancer cell, Cancer research, biology.protein, Female, Cell Division |
| الوصف: |
The transcription factor RE1 silencing transcription factor (REST) is lost in approximately 20% of breast cancers. Although it is known that these RESTless tumors are highly aggressive and include all tumor subtypes, the underlying tumorigenic mechanisms remain unknown. In this study, we show that loss of REST results in upregulation of LIN28A, a known promoter of tumor development, in breast cancer cell lines and human breast tumors. We found that LIN28A was a direct transcriptional target of REST in cancer cells and that loss of REST resulted in increased LIN28A expression and enhanced tumor growth both in vitro and in vivo, effects that were dependent on heightened LIN28A expression. Tumors lacking REST expression were locally invasive, consistent with the increased lymph node involvement observed in human RESTless tumors. Clinically, human RESTless breast tumors also displayed significantly enhanced LIN28A expression when compared with non-RESTless tumors. Our findings therefore show a critical role for the REST-LIN28A axis in tumor aggression and suggest a causative relationship between REST loss and tumorigenicity in vivo. Cancer Res; 72(13); 3207–16. ©2012 AACR. |
| تدمد: |
1538-7445 |
| URL الوصول: |
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f7d67afb215405243a44c0f50f29e95
https://pubmed.ncbi.nlm.nih.gov/22532168 |
| Rights: |
OPEN |
| رقم الانضمام: |
edsair.doi.dedup.....8f7d67afb215405243a44c0f50f29e95 |
| قاعدة البيانات: |
OpenAIRE |