AI Article Synopsis
- - The study investigates the role of long noncoding RNA LINC01534 in colorectal cancer (CRC), focusing on its relationship with cancer stemness and the endoplasmic reticulum (ER) stress response.
- - Experiments showed that silencing LINC01534 reduced cell growth, invasiveness, and cancer stemness, while activating the ER stress response via the PERK/eIF2α pathway.
- - High levels of LINC01534 expression in CRC samples were linked to poorer patient survival, suggesting it may serve as a potential prognostic factor in CRC.
Article Abstract
Background: Studies have shown that cancer stemness and the endoplasmic reticulum (ER) stress response are inversely regulated in colorectal cancer (CRC), but the mechanism has not been fully clarified. Long noncoding RNAs (lncRNAs) play key roles in cancer progression and metastasis. In this study we investigated lncRNA 01534 (LINC01534) as a possible modulator between cancer stemness and ER stress response.
Methods: In vitro experiments using CRC cell lines were performed to explore a possible role of LINC01534. The expression of LINC01534 in clinical CRC samples was assessed by quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and in situ hybridization.
Results: Silencing LINC01534 led to suppression of cell proliferation, invasiveness, and cell cycle progression at the G2-M phase, and promoted apoptosis. Moreover, we found that silencing LINC01534 suppressed cancer stemness, while it activated the ER stress response, especially through the PERK/eIF2α signaling pathway. In situ hybridization revealed LINC01534 was expressed in tumor cells and upregulated in CRC tissues compared with normal epithelium. A survival survey indicated that high LINC01534 expression was significantly associated with shorter overall survival in 187 CRC patients.
Conclusion: This is the first report on LINC01534 in human cancer. Our findings suggest that LINC01534 may be an important modulator of the maintenance of cancer stemness and suppression of the ER stress response, and that it could be a novel prognostic factor in CRC.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154865 | PMC |
| http://dx.doi.org/10.1002/ags3.12649 | DOI Listing |
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