LINC02878/ZNF282/PYCR2 axis promotes proline synthesis and tumor progression in colorectal cancer

Colorectal cancer (CRC) remains a leading cause of cancer-related mortality globally, with poor survival outcomes in advanced stages due to therapy resistance and metastasis. While long non-coding RNAs (lncRNAs) are emerging as key regulators of CRC progression, their functional interplay and metabolic implications remain poorly understood. Here, we identified LINC02878 as a novel oncogenic lncRNA significantly upregulated in CRC and correlated with poor prognosis. Mechanistically, LINC02878 binds to the ZNF282 to activate PYCR2 expression, thereby enhancing proline biosynthesis and driving tumor aggressiveness. In vivo, LINC02878 knockdown suppressed subcutaneous tumor growth, reduced lung metastasis, and improved survival in xenograft models. Our study unveils the LINC02878/ZNF282/PYCR2/proline axis as a critical metabolic vulnerability in CRC, offering potential therapeutic targets for intervention.

Authors

Institutions

Publication Details

Journal
Cellular and Molecular Life Sciences
Published
2025-12-02
DOI
https://doi.org/10.1007/s00018-025-05968-3
Citations
1
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
0.94
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

LINC02878/ZNF282/PYCR2 axis promotes proline synthesis and tumor progression in colorectal cancer

Song Shang, Binghu Lin, Junping Lei, Yu Guo et al.
1 citations
Cellular and Molecular Life Sciences
Cancer-related molecular mechanisms research
0.94
article

LINC02878/ZNF282/PYCR2 axis promotes proline synthesis and tumor progression in colorectal cancer

Song Shang, Binghu Lin, Junping Lei, Yu Guo, Michael Gong, Tian‐Yang Wang, Y. Li, Lin Wang, Jia Fu, Tian Xia, Yan Xu
article en
1 citations

Abstract

Colorectal cancer (CRC) remains a leading cause of cancer-related mortality globally, with poor survival outcomes in advanced stages due to therapy resistance and metastasis. While long non-coding RNAs (lncRNAs) are emerging as key regulators of CRC progression, their functional interplay and metabolic implications remain poorly understood. Here, we identified LINC02878 as a novel oncogenic lncRNA significantly upregulated in CRC and correlated with poor prognosis. Mechanistically, LINC02878 binds to the ZNF282 to activate PYCR2 expression, thereby enhancing proline biosynthesis and driving tumor aggressiveness. In vivo, LINC02878 knockdown suppressed subcutaneous tumor growth, reduced lung metastasis, and improved survival in xenograft models. Our study unveils the LINC02878/ZNF282/PYCR2/proline axis as a critical metabolic vulnerability in CRC, offering potential therapeutic targets for intervention.

Cellular and Molecular Life SciencesVol. 83(1)
Hubei University of Arts and Science (CN), Xiang Yang No.1 People's Hospital (CN)
Openalex Percentile: Top 18%
Cancer-related molecular mechanisms research
0.94
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.