Structural variation drives enhancer hijacking via 3D genome disruption in ccRCC - Takeaways - MDSpire
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Enhancer Hijacking in Clear Cell Renal Cell Carcinoma is Driven by Structural Variation and Disruption of 3D Genome Architecture

  • By

  • Yu Dong

  • Wenjiao Xia

  • Zitong Yang

  • Liangliang Ren

  • Hongru Wang

  • Yiyang Zhou

  • Qinchen Li

  • Zhi Chen

  • Zhinan Xia

  • Yichun Zheng

  • Feifan Wang

  • Ning He

  • Bing Cheng

  • Dongmei Ma

  • Wei Shao

  • Wei Guo

  • Shuwen Wang

  • Ziqiao Liu

  • Junxiao Shen

  • Yiming Qi

  • Xuke Gong

  • Juan Jin

  • Bo Xie

  • Guixin Zhu

  • Cheng Zhang

  • January 6, 2026

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  • 1

    Clear cell renal cell carcinoma (ccRCC) accounts for 70-80% of renal cell carcinoma cases and is characterized by high heterogeneity and aggressiveness.

  • 2

    Structural variants (SVs) significantly contribute to the genetic variation in ccRCC and can disrupt gene expression and regulatory networks.

  • 3

    Advancements in long-read sequencing technologies enable precise detection of SVs and their impact on 3D genome architecture in ccRCC.

  • 4

    The study identifies a novel enhancer hijacking event that activates the proto-oncogene SEMA5B, revealing new therapeutic targets.

  • 5

    A machine learning-based prognostic model developed from enhancer hijacking events shows robust predictive performance for ccRCC outcomes.

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