Squeezing ovarian cancer cells to predict metastatic potential

October 10, 2012 by Jason Maderer, Georgia Institute of Technology
An AFM, holding a microscale cantilever, is positioned just above a petri dish filled with ovarian cancer cells. Credit: Georgia Institute of Technology

(Medical Xpress)—New Georgia Tech research shows that cell stiffness could be a valuable clue for doctors as they search for and treat cancerous cells before they're able to spread. The findings, which are published in the journal PLoS One, found that highly metastatic ovarian cancer cells are several times softer than less metastatic ovarian cancer cells.

Assistant Professor Todd Sulchek and Ph.D. student Wenwei Xu used a process called (AFM) to study the mechanical properties of various ovarian cell lines. A soft mechanical probe "tapped" healthy, malignant and metastatic ovarian cells to measure their stiffness.

"In order to spread, must push themselves into the bloodstream. As a result, they must be highly deformable and softer," said Sulchek, a faculty member in the George W. Woodruff School of Mechanical Engineering. "Our results indicate that cell stiffness may be a useful biomarker to evaluate the relative metastatic potential of ovarian and perhaps other types of cancer cells."

Just as previous studies on other types of epithelial cancers have indicated, Sulchek also found that cancerous ovarian cells are generally softer and display lower intrinsic variability in cell stiffnesss than non-.

A triangular cantilever is positioned just over a metastatic ovarian cancer cell while preparing to indent and measure the stiffness. Credit: Georgia Institute of Technology

Sulchek's lab partnered with the molecular cancer lab of Biology Professor John McDonald, who is also director of Georgia Tech's newly established Integrated Cancer Research Center.

"This is a good example of the kinds of discoveries that only come about by integrating skills and knowledge from traditionally diverse fields such as molecular biology and bioengineering," said McDonald. "Although there are a number of developing methodologies to identify circulating cancer cells in the blood and other body fluids, this technology offers the added potential to rapidly determine if these cells are highly metastatic or relatively benign."

Sulchek and McDonald believe that, when further developed, this technology could offer a huge advantage to clinicians in the design of optimal chemotherapies, not only for ovarian cancer patients but also for patients of other types of cancer.

Explore further: Ovarian cancer stem cells targeted in new research

More information: dx.plos.org/10.1371/journal.pone.0046609

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