Integrin-Targeted Hybrid Fluorescence Molecular Tomography/X-ray Computed Tomography for Imaging Tumor Progression and Early Response in Non-Small Cell Lung Cancer

Bibliographic Details
Title: Integrin-Targeted Hybrid Fluorescence Molecular Tomography/X-ray Computed Tomography for Imaging Tumor Progression and Early Response in Non-Small Cell Lung Cancer
Authors: Xiaopeng Ma, Valerie Phi Van, Melanie A. Kimm, Jaya Prakash, Horst Kessler, Katja Kosanke, Annette Feuchtinger, Michaela Aichler, Aayush Gupta, Ernst J. Rummeny, Michel Eisenblätter, Jens Siveke, Axel K. Walch, Rickmer Braren, Vasilis Ntziachristos, Moritz Wildgruber
Source: Neoplasia: An International Journal for Oncology Research, Vol 19, Iss 1, Pp 8-16 (2017)
Publisher Information: Elsevier, 2017.
Publication Year: 2017
Collection: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
Subject Terms: Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
More Details: Integrins play an important role in tumor progression, invasion and metastasis. Therefore we aimed to evaluate a preclinical imaging approach applying ανβ3 integrin targeted hybrid Fluorescence Molecular Tomography/X-ray Computed Tomography (FMT-XCT) for monitoring tumor progression as well as early therapy response in a syngeneic murine Non-Small Cell Lung Cancer (NSCLC) model. Lewis Lung Carcinomas were grown orthotopically in C57BL/6 J mice and imaged in-vivo using a ανβ3 targeted near-infrared fluorescence (NIRF) probe. ανβ3-targeted FMT-XCT was able to track tumor progression. Cilengitide was able to substantially block the binding of the NIRF probe and suppress the imaging signal. Additionally mice were treated with an established chemotherapy regimen of Cisplatin and Bevacizumab or with a novel MEK inhibitor (Refametinib) for 2 weeks. While μCT revealed only a moderate slowdown of tumor growth, ανβ3 dependent signal decreased significantly compared to non-treated mice already at one week post treatment. ανβ3 targeted imaging might therefore become a promising tool for assessment of early therapy response in the future.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1476-5586
1522-8002
Relation: http://www.sciencedirect.com/science/article/pii/S147655861630210X; https://doaj.org/toc/1476-5586; https://doaj.org/toc/1522-8002
DOI: 10.1016/j.neo.2016.11.009
Access URL: https://doaj.org/article/cca4c019ff4249e8a2046ea0dbf7d60d
Accession Number: edsdoj.4c019ff4249e8a2046ea0dbf7d60d
Database: Directory of Open Access Journals
More Details
ISSN:14765586
15228002
DOI:10.1016/j.neo.2016.11.009
Published in:Neoplasia: An International Journal for Oncology Research
Language:English