TY - JOUR
T1 - Laser capture microdissection
AU - Liotta, Lance A.
AU - Conrads, Thomas P.
AU - Howard, Marissa A.
AU - Araujo, Robyn P.
AU - Petricoin, Emanuel F.
N1 - Publisher Copyright:
© Springer Nature Limited 2025.
PY - 2025/12
Y1 - 2025/12
N2 - The tissue microenvironment was once viewed as an impossibly complex heterogeneous ecosystem. Today, tools and data analysis methods probe tissues at multiple resolution levels, from subpopulations to individual cells and individual molecules. Laser capture microdissection (LCM) was one of the first technologies enabling spatial molecular interrogation in tissues, enabling the extraction of precise regions of tissue for downstream acquisition and analysis of multiple classes of molecular analytes — including nucleic acids, proteins, metabolites and lipids. By physically isolating targeted cells or tissue compartments under microscopic visualization, LCM preserves spatial context for downstream multiomic profiling. The approach is agnostic to tissue type, molecular target and analytical tool, providing a powerful platform for spatially resolved analysis of tissue heterogeneity, microenvironment interactions and region-specific signatures. The attributes of LCM have drawn a large and diverse community of users who have imaginatively elevated the technology and its applications far beyond the early versions of LCM. In this Primer, we provide examples of how and when to use LCM and discuss its use with other spatial profiling platforms, providing an essential component of large-scale clinical research trials, revealing disease mechanisms and identifying predictors of therapeutic efficacy. Finally, we explore how the next generation of LCM and companion technologies will help to shape the personalized, designer therapies of the future.
AB - The tissue microenvironment was once viewed as an impossibly complex heterogeneous ecosystem. Today, tools and data analysis methods probe tissues at multiple resolution levels, from subpopulations to individual cells and individual molecules. Laser capture microdissection (LCM) was one of the first technologies enabling spatial molecular interrogation in tissues, enabling the extraction of precise regions of tissue for downstream acquisition and analysis of multiple classes of molecular analytes — including nucleic acids, proteins, metabolites and lipids. By physically isolating targeted cells or tissue compartments under microscopic visualization, LCM preserves spatial context for downstream multiomic profiling. The approach is agnostic to tissue type, molecular target and analytical tool, providing a powerful platform for spatially resolved analysis of tissue heterogeneity, microenvironment interactions and region-specific signatures. The attributes of LCM have drawn a large and diverse community of users who have imaginatively elevated the technology and its applications far beyond the early versions of LCM. In this Primer, we provide examples of how and when to use LCM and discuss its use with other spatial profiling platforms, providing an essential component of large-scale clinical research trials, revealing disease mechanisms and identifying predictors of therapeutic efficacy. Finally, we explore how the next generation of LCM and companion technologies will help to shape the personalized, designer therapies of the future.
UR - http://www.scopus.com/inward/record.url?scp=105025808335&partnerID=8YFLogxK
U2 - 10.1038/s43586-025-00453-4
DO - 10.1038/s43586-025-00453-4
M3 - Review article
AN - SCOPUS:105025808335
SN - 2662-8449
VL - 5
JO - Nature Reviews Methods Primers
JF - Nature Reviews Methods Primers
IS - 1
M1 - 80
ER -