Accession Number:

ADA610228

Title:

Circumventing Therapeutic Resistance and the Emergence of Disseminated Breast Cancer Cells Through Non-Invasive Optical Imaging

Descriptive Note:

Annual rept. 1 Jul 2013-30 Jun 2014

Corporate Author:

DUKE UNIV MEDICAL CENTER DURHAM NC

Report Date:

2014-07-01

Pagination or Media Count:

27.0

Abstract:

Herein we explore a series of optically distinct near infrared emissive polymersomes NIREPs biodegradable polymer vesicles that manifest extraordinarily high irradiances and are ideally suited for in vivo optical imaging, each conjugated to different antibodies for the non-invasive molecular imaging of all breast cancer sites within a patient, including micrometastases. In Year 1, we have taken significant steps to optimize NIREP fabrication protocols to ensure immunoreactive antibodies can be reproducibly conjugated to the surface of NIREPs. We have designed and synthesized the most extensive family of PEO-b- PCL copolymers that vary over the largest range of number-average molecular weights Mn 3.6 - 57K, PEO weight fractions fPEO 0.08 - 0.33, and PEO chain lengths 0.75 5.8K reported to date. With these, we have demonstrated using comparative morphology diagrams, that a multiplicity of PEO-b-PCL diblock copolymer compositions are able to give rise to nanoscale vesicles. The broad range of polymersome-forming PEO-b-PCL compositions suggest the ability to construct extensive families of nanoscale vesicles of varied bilayer thickness, providing the ability to tune the timescales of vesicle degradation in vivo. Lastly, we have established four pairs of parental and isogenic matched tamoxifen tam-resistant cell lines MCF7, T47D, MDA-MB-361 and HCC1428, and characterized the changes in cell surface protein expression that occurs with onset of resistance. We have found that members of the HER receptor family EGFRHER1 HER2 HER3 are upregulated with the development of tam-resistance furthermore, differences in receptor expression between ER cell lines have been characterized. These reagents are critical for evaluation of the selectivity of a panel of antibody-conjugated NIREPs.

Subject Categories:

  • Medicine and Medical Research

Distribution Statement:

APPROVED FOR PUBLIC RELEASE