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Nanoneedle arrays map RNA in fresh tissue without sequencing or amplification

Nanoneedle arrays map RNA in fresh tissue without sequencing or amplification

phys.org 04.10.2026 23:00 7 views
Recently, spatial omics has become a powerful tool, enabling researchers to see not only what molecules are present in a tissue, but also where they are located and how they are organized across cells, tissue structures

This article has been reviewed according to Science X's editorial process and policies. Editors have highlighted the following attributes while ensuring the content's credibility: Recently, spatial omics has become a powerful tool, enabling researchers to see not only what molecules are present in a tissue, but also where they are located and how they are organized across cells, tissue structures and local microenvironments. This spatial context has deepened our understanding of cancer, neurobiology and immunology.

Yet as the field advances, an important question remains: How many of these powerful technologies are ready for routine clinical use? The most informative technologies are often the most demanding, requiring expensive instruments, sequencing, complicated tissue preparation, lengthy workflows and substantial computational resources. While these requirements are manageable in well-resourced research settings, they can become major obstacles in pathology laboratories, where time-sensitive biopsies, clinical practicality and broad patient access are critical considerations.

To address this challenge, a research team led by Shi Peng, a professor in the Department of Biomedical Engineering in the College of Biomedicine at City University of Hong Kong (CityUHK), has presented Spectrum-FISH, a sequencing-free and amplification-free approach to spatial tissue analysis. The method is based on a "touch-and-go" molecular fishing strategy that uses vertically aligned nanoprobes. Unlike existing spatial omics technologies, which typically require extensive tissue pretreatment, Spectrum-FISH can be applied directly to freshly prepared tissue samples.

Spatial information is preserved through a registration strategy that allows researchers to map molecular signals back to tissue structures and individual cells. Using experiments involving the developing mouse neural tube and olfactory bulb and fresh human colorectal biopsy specimens, the research team investigated whether spatial profiling could be made more accessible by reducing dependence on sequencing, minimizing tissue processing and lowering assay costs while maintaining biologically informative resolution. Spectrum-FISH's compatibility with fresh tissues and sequencing-free design offer advantages in affordability and scalability.

Its coordinate-preserving sampling strategy also points to new possibilities for spatial analysis in live or minimally processed tissues. Moreover, its ability to profile messenger RNAs (mRNAs), microRNAs (miRNAs) and RNA methylation provides a potential pathway toward spatial multi-omics that are less dependent on large-scale sequencing infrastructure. The findings were published recently in Nature Biomedical Engineering in a paper titled "Sequencing-free spatial profiling of post-transcriptional regulation in fresh tissues using nanoneedle arrays".

The study aligns closely with the themes discussed in a recent comment article, "Clinical translation of spatial omics", co-authored by Shi and published in Nature Reviews Bioengineering. Together, the two publications underscore the growing momentum toward the clinical translation of spatial omics. "This project reminded us that innovation in biomedicine is about more than enabling measurements; it must also ensure they are practical and accessible," said Shi.

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