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NCBP2 drives colorectal cancer growth and metastasis through LIPG-mediated lipid droplet accumulation
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  • Published: 24 March 2026

NCBP2 drives colorectal cancer growth and metastasis through LIPG-mediated lipid droplet accumulation

  • Liu Liu1 na1,
  • Wei Lu2 na1,
  • Shengyuan Miao2 na1,
  • Yang Yu2,
  • Xu-bing Zhang1,
  • ShouDong Ye  ORCID: orcid.org/0000-0003-1864-85612,
  • Xiaoxiao Wang  ORCID: orcid.org/0000-0001-8496-48753 &
  • …
  • Lin Liu  ORCID: orcid.org/0000-0003-4125-92573 

Communications Biology , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Cancer metabolism
  • Colon cancer

Abstract

RNA-binding proteins play critical roles in RNA processing and are aberrantly expressed in colorectal cancer (CRC). Through comprehensive analysis of multiple gene expression datasets (GSE20916, GSE18105, GSE21510, TCGA-COAD and TCGA-READ), NCBP2 was identified as a potential tumorigenic gene in CRC. NCBP2 expression was significantly elevated in CRC tissues, correlated with tumour invasion and metastasis, and associated with poor patient survival outcomes. Furthermore, overexpression of NCBP2 in CRC cells was shown to increase cell proliferation, migration, and tumour invasion in both in vitro and in vivo models. Mechanistically, the NCBP2 protein stabilised LIPG mRNA via direct binding to the m7G motif in the 5’-cap structure of LIPG mRNA, thereby increasing LIPG expression. Additionally, NCBP2 promoted lipid droplet accumulation in CRC cells in a LIPG-dependent manner. These findings collectively suggest that the NCBP2-LIPG-lipid droplet axis represents a novel mechanism underlying CRC progression and metastasis, providing a promising therapeutic target for CRC treatment.

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Data availability

All uncropped blots are provided in Supplementary information. The source data behind the graphs in the manuscript can be found in Supplementary Data 1. Data related to mRNA sequence analysis have been deposited in the GEO, and the accession number is GSE270402. All other data supporting the findings of this study are available from the corresponding author upon reasonable request.

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Acknowledgements

This study was supported by the USTC Research Funds of the Double First-Class Initiative (No. YD9110002066), the Research Funds of the Centre for Leading Medicine and Advanced Technologies of IHM (2023IHM01092), and the Natural Science Foundation of Anhui Province (2308085QC84).

Author information

Author notes
  1. These authors contributed equally: Liu Liu, Wei Lu, Shengyuan Miao.

Authors and Affiliations

  1. Department of General Surgery, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China

    Liu Liu & Xu-bing Zhang

  2. Center for Stem Cell and Translational Medicine, School of Life Sciences, Anhui University, Hefei, China

    Wei Lu, Shengyuan Miao, Yang Yu & ShouDong Ye

  3. Department of Anaesthesiology, the First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China

    Xiaoxiao Wang & Lin Liu

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Contributions

Liu Liu, X.X. Wang and Lin Liu designed the study; Liu Liu, W. Lu, S.Y. Miao, Y.Yu and X.B. Zhang conducted the experiments and analysed the data; Liu Liu, W. Lu, Y. Yu and S.Y. Miao prepared the figures and drafted the manuscript. S.D. Ye and Lin Liu reviewed and revised the manuscript. All the authors have read and approved the final version of the manuscript.

Corresponding authors

Correspondence to Xiaoxiao Wang or Lin Liu.

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The authors declare no competing interests.

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Communications Biology thanks the anonymous reviewers for their contribution to the peer review of this work. Primary Handling Editors: Georgios Giamas and Johannes Stortz. [A peer review file is available].

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Supplementary information

Transparent Peer Review file (download PDF )

Supplementary information (download PDF )

Description of Additional Supplementary Files (download PDF )

Supplementary Data 1 (download XLSX )

nr-reporting-summary (download PDF )

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Liu, L., Lu, W., Miao, S. et al. NCBP2 drives colorectal cancer growth and metastasis through LIPG-mediated lipid droplet accumulation. Commun Biol (2026). https://doi.org/10.1038/s42003-026-09903-5

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  • Received: 25 February 2025

  • Accepted: 10 March 2026

  • Published: 24 March 2026

  • DOI: https://doi.org/10.1038/s42003-026-09903-5

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