Single-cell transcriptomics in cancer: computational challenges and opportunities

Intratumor heterogeneity is a common characteristic across diverse cancer types and presents challenges to current standards of treatment. Advancements in high-throughput sequencing and imaging technologies provide opportunities to identify and characterize these aspects of heterogeneity. Notably, transcriptomic profiling at a single-cell resolution enables quantitative measurements of the molecular activity that underlies the phenotypic diversity of cells within a tumor. Such high-dimensional data require computational analysis to extract relevant biological insights about the cell types and states that drive cancer development, pathogenesis, and clinical outcomes. In this review, we highlight emerging themes in the computational analysis of single-cell transcriptomics data and their applications to cancer research. We focus on downstream analytical challenges relevant to cancer research, including how to computationally perform unified analysis across many patients and disease states, distinguish neoplastic from nonneoplastic cells, infer communication with the tumor microenvironment, and delineate tumoral and microenvironmental evolution with trajectory and RNA velocity analysis. We include discussions of challenges and opportunities for future computational methodological advancements necessary to realize the translational potential of single-cell transcriptomic profiling in cancer. By analyzing gene expression patterns in individual tumor cells, researchers can gain patient-specific insights that might inform more effective cancer treatment. Tumors are highly dynamic and heterogeneous collections of cells. Single-cell transcriptomics techniques can offer a valuable window into that complexity but only if the appropriate computational tools are used to analyze the data. Jean Fan of Harvard University, Cambridge, USA, and colleagues have reviewed some of these computational strategies and how they can be employed in cancer research. Single-cell analysis algorithms, for example, can reveal characteristics that distinguish healthy cells from cancerous cells, or indicate how the cells within the tumor may be communicating with each other to promote malignant growth. These are still new technologies, however, and the authors highlight the limitations of the conclusions that can currently be drawn from such analyses.

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