AI Article Synopsis

  • The study introduces a new multimodal nanosensor that targets tumors using acidity levels, allowing for early detection and monitoring of cancer response to treatment in mouse models of colorectal cancer.
  • This sensor can non-invasively assess tumor progression and therapy response by releasing urinary reporters in response to specific proteases in the tumor microenvironment.
  • By combining a radiotracer for tumor imaging with customizable features, the platform aims to support personalized treatment strategies for various cancer types.

Article Abstract

Therapeutic outcomes in oncology may be aided by precision diagnostics that offer early detection, localization and the opportunity to monitor response to therapy. Here, we report a multimodal nanosensor engineered to target tumours through acidosis, respond to proteases in the microenvironment to release urinary reporters and (optionally) carry positron emission tomography probes to enable localization of primary and metastatic cancers in mouse models of colorectal cancer. We present a paradigm wherein this multimodal sensor can be employed longitudinally to assess burden of disease non-invasively, including tumour progression and response to chemotherapy. Specifically, we showed that acidosis-mediated tumour insertion enhanced on-target release of matrix metalloproteinase-responsive reporters in urine. Subsequent on-demand loading of the radiotracer Cu allowed pH-dependent tumour visualization, enabling enriched microenvironmental characterization when compared with the conventional metabolic tracer F-fluorodeoxyglucose. Through tailored target specificities, this modular platform has the capacity to be engineered as a pan-cancer test that may guide treatment decisions for numerous tumour types.

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Source
http://dx.doi.org/10.1038/s41563-021-01042-yDOI Listing

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