LINC00461 promotes bladder cancer cells EMT through miR-518b/HNRNPUL1 axis

Bladder cancer (BC) is a prevalent type of tumor in the urinary system, and it has been discovered that long non-coding RNA (lncRNA) plays a significant role in its occurrence and development. However, thus far, no reports have been published on the involvement of LINC00461 in BC. Here, we found that LINC00461 levels were upregulated in BC tissues and cell lines. Besides, knockdown of LINC00461 inhibited BC cell proliferation, migration, invasion through epithelial-mesenchymal transition (EMT), and slowed down tumor growth in vivo. Moreover, we found that LINC00461 regulated HNRNPUL1 expression through miR-518b sponge activity, and the miR-518 inhibitor could reverse the inhibitory effects of LINC00461 knockdown on BC cell proliferation, migration, and EMT. Our results suggest that LINC00461 may serve as a potential biomarker and therapeutic target for BC.

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Publication Details

Journal
Discover Oncology
Published
2024-09-10
DOI
https://doi.org/10.1007/s12672-024-01294-5
Citations
1
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
0.29
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article

LINC00461 promotes bladder cancer cells EMT through miR-518b/HNRNPUL1 axis

Jing Jin, Yijie Zhou, Jiajun Chen, Shouhua Pan et al.
1 citations
Discover Oncology
Cancer-related molecular mechanisms research
0.29
article

LINC00461 promotes bladder cancer cells EMT through miR-518b/HNRNPUL1 axis

Jing Jin, Yijie Zhou, Jiajun Chen, Shouhua Pan, Junlong Li, Keyuan Zhao, Chao Peng, Gang Xu, Yulei Li
article en
1 citations

Abstract

Bladder cancer (BC) is a prevalent type of tumor in the urinary system, and it has been discovered that long non-coding RNA (lncRNA) plays a significant role in its occurrence and development. However, thus far, no reports have been published on the involvement of LINC00461 in BC. Here, we found that LINC00461 levels were upregulated in BC tissues and cell lines. Besides, knockdown of LINC00461 inhibited BC cell proliferation, migration, invasion through epithelial-mesenchymal transition (EMT), and slowed down tumor growth in vivo. Moreover, we found that LINC00461 regulated HNRNPUL1 expression through miR-518b sponge activity, and the miR-518 inhibitor could reverse the inhibitory effects of LINC00461 knockdown on BC cell proliferation, migration, and EMT. Our results suggest that LINC00461 may serve as a potential biomarker and therapeutic target for BC.

Discover OncologyVol. 15(1)
Shaoxing People's Hospital (CN)
Good health and well-being
Openalex Percentile: Top 40%
Cancer-related molecular mechanisms research
0.29
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LINC00461 promotes bladder cancer cells EMT through miR-518b/HNRNPUL1 axis — Jing Jin, Yijie Zhou, et al. · Discover Oncology (2024) | TGRS Research Map | TGRS