4.8 Article

Spatiotemporal analysis of glioma heterogeneity reveals COL1A1 as an actionable target to disrupt tumor progression

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NATURE COMMUNICATIONS
卷 13, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41467-022-31340-1

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资金

  1. National Institutes of Health, National Institute of Neurological Disorders and Stroke (NIH/NINDS) [R37-NS094804, R01-NS105556, R21-NS107894, R21-NS091555, R01-NS074387]
  2. National Institute of Neurological Disorders and Stroke (NIH/NINDS) [R01-NS076991, R01-NS096756, R01-NS082311, R01-NS122234, R01-NS127378]
  3. National Institute of Biomedical Imaging and Bioengineering (NIH/NIBI) [R01-EB022563]
  4. National Cancer Institute (NIH/NCI) [U01CA224160, R01 CA125577, R01 CA107469]
  5. Rogel Cancer Center at The University of Michigan [G023089]
  6. Ian's Friends Foundation [G024230]
  7. Leah's Happy Hearts Foundation [G013908]
  8. Pediatric Brain Tumor Foundation [G023387]
  9. ChadTough Foundation [G023419]
  10. RNA Biomedicine grant [F046166]
  11. Health and Human Services, National Institutes of Health [UL1 TR002240, F049768]

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This study investigates the dynamic anatomical structures called oncostreams in high grade gliomas (HGG) and their regulation by COL1A1. The researchers found that oncostreams play a role in tumor growth and aggression, facilitating the distribution of tumor and non-tumor cells within the tumor and potentially contributing to the invasion of normal brain tissue. They also discovered that COL1A1 is a central gene in the organization of oncostreams and a powerful regulator of glioma malignant behavior. Inhibiting COL1A1 can eliminate oncostreams and alter the tumor microenvironment, leading to reduced expression of mesenchymal associated genes and extended survival in animal models.
It is essential to improve our understanding of the features that influence aggressiveness and invasion in high grade gliomas (HGG). Here, the authors characterize dynamic anatomical structures in HGG called oncostreams, which are associated with tumor growth and are regulated by COL1A1. Intra-tumoral heterogeneity is a hallmark of glioblastoma that challenges treatment efficacy. However, the mechanisms that set up tumor heterogeneity and tumor cell migration remain poorly understood. Herein, we present a comprehensive spatiotemporal study that aligns distinctive intra-tumoral histopathological structures, oncostreams, with dynamic properties and a specific, actionable, spatial transcriptomic signature. Oncostreams are dynamic multicellular fascicles of spindle-like and aligned cells with mesenchymal properties, detected using ex vivo explants and in vivo intravital imaging. Their density correlates with tumor aggressiveness in genetically engineered mouse glioma models, and high grade human gliomas. Oncostreams facilitate the intra-tumoral distribution of tumoral and non-tumoral cells, and potentially the collective invasion of the normal brain. These fascicles are defined by a specific molecular signature that regulates their organization and function. Oncostreams structure and function depend on overexpression of COL1A1. Col1a1 is a central gene in the dynamic organization of glioma mesenchymal transformation, and a powerful regulator of glioma malignant behavior. Inhibition of Col1a1 eliminates oncostreams, reprograms the malignant histopathological phenotype, reduces expression of the mesenchymal associated genes, induces changes in the tumor microenvironment and prolongs animal survival. Oncostreams represent a pathological marker of potential value for diagnosis, prognosis, and treatment.

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