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A flexible electronic strain sensor for the real-time monitoring of tumor regression.


ABSTRACT: Assessing the efficacy of cancer therapeutics in mouse models is a critical step in treatment development. However, low-resolution measurement tools and small sample sizes make determining drug efficacy in vivo a difficult and time-intensive task. Here, we present a commercially scalable wearable electronic strain sensor that automates the in vivo testing of cancer therapeutics by continuously monitoring the micrometer-scale progression or regression of subcutaneously implanted tumors at the minute time scale. In two in vivo cancer mouse models, our sensor discerned differences in tumor volume dynamics between drug- and vehicle-treated tumors within 5 hours following therapy initiation. These short-term regression measurements were validated through histology, and caliper and bioluminescence measurements taken over weeklong treatment periods demonstrated the correlation with longer-term treatment response. We anticipate that real-time tumor regression datasets could help expedite and automate the process of screening cancer therapies in vivo.

SUBMITTER: Abramson A 

PROVIDER: S-EPMC9481124 | biostudies-literature | 2022 Sep

REPOSITORIES: biostudies-literature

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A flexible electronic strain sensor for the real-time monitoring of tumor regression.

Abramson Alex A   Chan Carmel T CT   Khan Yasser Y   Mermin-Bunnell Alana A   Matsuhisa Naoji N   Fong Robyn R   Shad Rohan R   Hiesinger William W   Mallick Parag P   Gambhir Sanjiv Sam SS   Bao Zhenan Z  

Science advances 20220916 37


Assessing the efficacy of cancer therapeutics in mouse models is a critical step in treatment development. However, low-resolution measurement tools and small sample sizes make determining drug efficacy in vivo a difficult and time-intensive task. Here, we present a commercially scalable wearable electronic strain sensor that automates the in vivo testing of cancer therapeutics by continuously monitoring the micrometer-scale progression or regression of subcutaneously implanted tumors at the min  ...[more]

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