Cancer cells survival is dependent on the lincRNA JUNI
Shaulian, E.; Kumar, V.; Soni, I.; Stern, E.; Ginsberg, D.; Dodel, M.; Mardakheh, F. K.; Vias, C.; Sabate-Cadenas, X.; Shkumatava, A.
Show abstract
Identification of key factors for cellular survival is a basis for therapy. We identified JUNI (linc01135) as a stress-regulated lncRNA, essential for cell survival and implicated in cancer. Besides regulating c-Jun expression we demonstrate c-Jun-independent, robust requirement for cell survival. Analysis of median survival of cancer patients suffering from various types of cancer reveals correlations of JUNI expression levels with alterations in patients survival. JUNIs antagonistic interaction with DUSP14, a negative regulator of the JNK pathway, underlies the regulation of c-Jun and partial effects on cellular survival. Consistently, DUSP14 expression is coherently inversely-correlated with the survival of patients suffering from the same types of cancer. Our data suggests that JUNI is a novel master regulator of cell fate. SummaryJUNI is a novel regulator of cell survival, JNK activation and c-Jun expression, implicated in survival of cancer patients
Matching journals
The top 12 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- Replication stress and FOXM1 drive radiation induced genomic instability and cell transformation 94%
- Defective base excision repair in the response to DNA damaging agents in triple negative breast cancer 93%
- Altering mammalian transcription networking with ADAADi: An inhibitor of ATP-dependent chromatin remodeling 92%
Similar papers in this journal
- eIF2α integrates proteotoxic signals both from ER and cytoplasm: Hsp70-Bag3 module regulates HRI-dependent phosphorylation of eIF2α 91%
- A long intergenic non-coding RNA regulates nuclear localisation of DNA methyl transferase-1 91%
- RNA Helicase DDX3 Regulates RAD51 Localization and DNA Damage Repair in Ewing Sarcoma 91%
Similar papers in this journal
- The anti-tumor effect of trifluridine via induction of aberrant mitosis is unaffected by mutations modulating p53 activity 92%
- NSD1 supports cell growth and regulates autophagy in HPV-negative head and neck squamous cell carcinoma. 92%
- The oncogenic E3 ligase TRIP12 suppresses epithelial-mesenchymal transition (EMT) and metastasis-related processes through ZEB1/2 91%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.