High-throughput, label-free, single-cell photoacoustic microscopy of intratumoral metabolic heterogeneity

Intratumoral heterogeneity, which is manifested in almost all of the hallmarks of cancer, including the significantly altered metabolic profiles of cancer cells, represents a challenge to effective cancer therapy. High-throughput measurements of the metabolism of individual cancer cells would allow...

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Veröffentlicht in:Nature biomedical engineering 2019-05, Vol.3 (5), p.381-391
Hauptverfasser: Hai, Pengfei, Imai, Toru, Xu, Song, Zhang, Ruiying, Aft, Rebecca L., Zou, Jun, Wang, Lihong V.
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Sprache:eng
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Zusammenfassung:Intratumoral heterogeneity, which is manifested in almost all of the hallmarks of cancer, including the significantly altered metabolic profiles of cancer cells, represents a challenge to effective cancer therapy. High-throughput measurements of the metabolism of individual cancer cells would allow direct visualization and quantification of intratumoral metabolic heterogeneity, yet the throughputs of current measurement techniques are limited to about 120 cells per hour. Here, we show that single-cell photoacoustic microscopy can reach throughputs of approximately 12,000 cells per hour by trapping single cells with blood in an oxygen-diffusion-limited high-density microwell array and by using photoacoustic imaging to measure the haemoglobin oxygen change (that is, the oxygen consumption rate) in the microwells. We demonstrate the capability of this label-free technique by performing high-throughput single-cell oxygen-consumption-rate measurements of cultured cells and by imaging intratumoral metabolic heterogeneity in specimens from patients with breast cancer. High-throughput single-cell photoacoustic microscopy of oxygen consumption rates should enable the faster characterization of intratumoral metabolic heterogeneity. Single-cell photoacoustic microscopy can perform high-throughput measurements of intratumoral metabolic heterogeneity in specimens from patients with breast cancer.
ISSN:2157-846X
2157-846X
DOI:10.1038/s41551-019-0376-5