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2010 Annual Report - Cancer Research Center

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Current <strong>Research</strong><br />

site. Nanoparticle work, including testing different nanoparticles and drug formulations, will continue in<br />

2011 and improve the cancer-killing effectiveness of our BCT therapy. (Figure 2) In addition to carrying additional<br />

cancer therapies to the tumor site, nanoparticles can also be used as an important cancer-detection<br />

diagnostic tool as they are easily detected in the body and will be used to confirm that the therapy being<br />

used is properly concentrating at the tumor site inside our animal cancer model and eventually, our clinical<br />

cancer patient.<br />

Work on the BCT therapy to date has attracted the interest of other cancer research facilities, including<br />

Immunophotonics, Inc. The CRC has entered into a collaboration with Immunophotonics to determine if<br />

BCT therapy can be successfully combined with Immunophotonics, Inc. therapeutic technologies that are<br />

already in FDA clinical testing for use in the USA and being successfully used in clinics in Peru. We are<br />

continuing this research partnership in 2011.<br />

We also continue to search for and select bacterial<br />

strains with improved targeting capabilities. In <strong>2010</strong>,<br />

visiting CRC Scholar Dr. Chengzhi Wang developed<br />

an improved protocol for generating strains<br />

that target prostate cancers in our animal prostate<br />

cancer model and is continuing his work to make<br />

a better targeting strain in 2011. Dr. Kazmierczak,<br />

with the assistance of our CRC student interns, is<br />

selecting and screening new bacterial species for<br />

their ability to attach to human prostate cancer<br />

cells in culture. (Figure 3) This work is expected to<br />

continue throughout 2011 and will yield important<br />

information about the nature of bacterial attraction<br />

to cancer cells and tumor masses. As strain generation<br />

progresses we will also be looking for stains with<br />

targeting ability for melanoma , pancreatic, colon<br />

and breast cancers. This work will be done in tissue<br />

culture and will lay the groundwork for approval for<br />

animal model studies of these cancer types in the<br />

future.<br />

Figure 3 Attachment of nanoparticles<br />

on outer perimeter of cancer targeting (2631) cells.<br />

Each year we build on the success of previous years<br />

as we continue the development of a bacterial cancer therapy. It seems like only yesterday the idea of scouring<br />

our unique collection of archival Salmonella for a new weapon against cancer was born. Thanks to our<br />

generous supporters and hard work our Salmonella-based bacterial cancer therapy is making great progress<br />

on the way to becoming an effective treatment in the fight against cancer.<br />

Coley, W. 1929. The cancer symposium at Lake Mohonk. Am. J. Surg. 1:22-23.<br />

Friberg, S. 1993. BCG in the treatment of superficial cancer of the bladder: a review. Med Oncol Tumor<br />

Pharmacother 10:31-6.<br />

A year in review <strong>2010</strong> 13

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