22 June 2023 | Thursday | Analysis
Source : PerkinElmer
Fluorescence imaging offers researchers a unique opportunity to understand the early biological changes associated with disease development, therapeutic efficacy, and drug-induced tissue changes. Traditionally, tumor burden, a measurement of the amount of cancer present, has been evaluated using caliper measurements or bioluminescence. This approach relies on gross overt changes in tumor size as a late indicator of treatment efficacy. However, it fails to capture the early biological changes that can be predictive of the later changes in tumor volume.
Certainly, relying solely on the gross measurement of tumor size to assess treatment efficacy can be misleading. Factors such as infiltrating inflammatory cells, calcified parts, and necrotic tissue can obscure treatment effects on viable tumor tissue, resulting in an inaccurate representation of treatment response.
Fluorescence imaging offers a more holistic view of tumor biology, revealing sensitive and timely assessments of changes in tumor growth, tumor metabolism, protease activity, inflammation, cell death, and hypoxia. By employing well-defined fluorescent probes, researchers can detect and quantify treatment-induced changes in tumor biology before they manifest as changes in tumor volume. This early detection not only enhances our understanding of the disease but also enables adjustments to be made to treatment strategies, leading to more effective interventions and the possibility of developing more targeted and personalized therapies.
To gain a complete understanding of tumor biology, it is critical to identify when specific biomarkers are active, as cancer biomarkers may exhibit fluctuations in expression throughout the development of a tumor and may significantly impact growth. A recent case study reported the results of imaging two different tumor types using distinct fluorescent agents capable of detecting protease activity or surface receptor expression.
In this case study, fluorescence quantification with multiple probes highlights the significance of considering characteristic differences in rates of protease expression in tumors when selecting the appropriate probes, or conversely the significance of using probes to detect differences in protease expression. Specifically, lower protease activity was observed early on in one tumor type, while similar levels of integrin receptor expression, an indicator of tumor burden, were observed across the tumors. Comprehensive tumor profiling therefore not only aids in accurate assessment of tumor burden but also proves valuable for the biological characterization of tumors, facilitating the development of targeted therapeutic interventions.
By employing well-defined and validated fluorescent probes, researchers can not only assess tumor burden, but also detect specific biomarkers and monitor treatment efficacy in a noninvasive and sensitive manner. This technology provides valuable insights into early biological changes, enabling timely go/no-go decisions on which drug candidates to invest in for further development.
At Revvity, our IVISense™ in vivo fluorescent imaging probes are important tools to noninvasively detect and quantify biomarkers such as protease activity to study early biological changes beyond just measuring tumor burden. To help inform your decisions and drive your oncology research forward, we have developed an interactive Selector Guide for IVISense™ fluorescent probes for assessing growth, metabolism, protease activity, inflammation, cell death, hypoxia, and other important aspects of tumor biology.
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