Degree Type

Honors Capstone Project

Date of Submission

Spring 5-1-2019

Capstone Advisor

Thomas Fondy

Honors Reader

Michael Sponsler

Capstone Major

Biology

Capstone College

Arts and Science

Audio/Visual Component

no

Capstone Prize Winner

no

Won Capstone Funding

no

Honors Categories

Sciences and Engineering

Subject Categories

Biochemistry, Biophysics, and Structural Biology | Cancer Biology | Life Sciences

Abstract

Research in the Fondy laboratory at Syracuse University has shown that in free-moving cancer cell lines, such as leukemia and lymphoma, larger cells are preferentially targeted by ultrasound therapy and have reduced viability as a result. Little time with respect to ultrasound, however, has been dedicated to the study of cell lines such as colorectal carcinoma and glioblastoma, which require connective tissue to grow.

Our research involves the low-frequency ultrasound treatment of attached carcinoma cell lines with adjuvant chemotherapy to evaluate an effective regimen for reducing viability of cancer cells. Prior research with human glioblastoma has shown that cells attached to a polystyrene plate are readily detached from their connective surface if provided with enough cavitation power from sonication. We plated, sonicated, and determined cell viability and number of RKO (human colorectal cancer) and hLN18 (human glioblastoma) in the 20kHz frequency range to evaluate effectiveness of sonodynamic therapy. These procedures were augmented by treatment with cytoskeleton-directed agent cytochalasin B (CB) either several days prior to or immediately following treatment to determine if sonication improves the chemotherapeutic properties of CB and vice versa. We additionally compared the sonication of RKO to cell detachment with trypsin, the latter of which is a technique commonly used in passaging attached cell lines, to determine if a statistically significant difference between the techniques implies a usefulness for sonodynamic treatment.

Early results imply that ultrasound significantly reduces cell viability when concentrated over a small region of cells. While the risk of metastasis is not known, we have assayed for apoptosis in sonicated cells to determine the proportion of cells at risk for metastasis. Trypsin treatment is near statistically significantly different for reducing viability compared to sonication with a relatively small sample size.

Creative Commons License

Creative Commons Attribution 4.0 International License
This work is licensed under a Creative Commons Attribution 4.0 International License.

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