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Mapping lesion-specific response and progression dynamics and inter-organ variability in metastatic colorectal cancer

Author

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  • Jiawei Zhou

    (University of North Carolina at Chapel Hill)

  • Amber Cipriani

    (University of North Carolina at Chapel Hill
    UNC Health Medical Center, Department of Pharmacy)

  • Yutong Liu

    (University of North Carolina at Chapel Hill)

  • Gang Fang

    (University of North Carolina at Chapel Hill)

  • Quefeng Li

    (University of North Carolina at Chapel Hill)

  • Yanguang Cao

    (University of North Carolina at Chapel Hill
    University of North Carolina at Chapel Hill)

Abstract

Achieving systemic tumor control across metastases is vital for long-term patient survival but remains intractable in many patients. High lesion-level response heterogeneity persists, conferring many dissociated responses across metastatic lesions. Most studies of metastatic disease focus on tumor molecular and cellular features, which are crucial to elucidating the mechanisms underlying lesion-level variability. However, our understanding of lesion-specific heterogeneity on the macroscopic level, such as lesion dynamics in growth, response, and progression during treatment, remains rudimentary. This study investigates lesion-specific response heterogeneity through analyzing 116,542 observations of 40,612 lesions in 4,308 metastatic colorectal cancer (mCRC) patients. Despite significant differences in their response and progression dynamics, metastatic lesions converge on four phenotypes that vary with anatomical site. Importantly, we find that organ-level progression sequence is closely associated with patient long-term survival, and that patients with the first lesion progression in the liver often have worse survival. In conclusion, our study provides insights into lesion-specific response and progression heterogeneity in mCRC and creates impetus for metastasis-specific therapeutics.

Suggested Citation

  • Jiawei Zhou & Amber Cipriani & Yutong Liu & Gang Fang & Quefeng Li & Yanguang Cao, 2023. "Mapping lesion-specific response and progression dynamics and inter-organ variability in metastatic colorectal cancer," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-36121-y
    DOI: 10.1038/s41467-023-36121-y
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    1. Maximilian Merz & Almuth Maria Anni Merz & Jie Wang & Lei Wei & Qiang Hu & Nicholas Hutson & Cherie Rondeau & Kimberly Celotto & Ahmed Belal & Ronald Alberico & AnneMarie W. Block & Hemn Mohammadpour , 2022. "Deciphering spatial genomic heterogeneity at a single cell resolution in multiple myeloma," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    2. Karama Asleh & Gian Luca Negri & Sandra E. Spencer Miko & Shane Colborne & Christopher S. Hughes & Xiu Q. Wang & Dongxia Gao & C. Blake Gilks & Stephen K. L. Chia & Torsten O. Nielsen & Gregg B. Morin, 2022. "Proteomic analysis of archival breast cancer clinical specimens identifies biological subtypes with distinct survival outcomes," Nature Communications, Nature, vol. 13(1), pages 1-19, December.
    3. Fengying Wu & Jue Fan & Yayi He & Anwen Xiong & Jia Yu & Yixin Li & Yan Zhang & Wencheng Zhao & Fei Zhou & Wei Li & Jie Zhang & Xiaosheng Zhang & Meng Qiao & Guanghui Gao & Shanhao Chen & Xiaoxia Chen, 2021. "Single-cell profiling of tumor heterogeneity and the microenvironment in advanced non-small cell lung cancer," Nature Communications, Nature, vol. 12(1), pages 1-11, December.
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