Tuesday, October 27, 2009

Stacks Of Filter Paper Provide A Realistic, Easy-to-use Medium For Growing Cells

An insight from the labs of Harvard chemist George Whitesides and cell biologist Don Ingber is likely to make a fundamental shift in how biologists grow and study cells – and it's as cheap and simple as reaching for a paper towel.

Ratmir Derda, a postdoctoral student co-mentored by Whitesides and Ingber at Harvard's new Wyss Institute for Biologically Inspired Engineering, has realized that by growing cells on several sheets of uncoated paper, he can solve a problem that has bedeviled biologists for years: how to easily grow and study cells that mimic the three-dimensionality of real tissue.

This work will simplify creation of realistic, three-dimensional models of normal or cancerous tissue -- potentially making it faster and easier to find drugs that fight cancer and other diseases.

"This research has the potential to become a standard laboratory tool, alongside the Petri dish, in laboratories that work with cells," said George M. Whitesides, the Woodford L. and Ann A. Flowers University Professor at Harvard University and a founding faculty member of the Wyss Institute. "Filter paper and other kinds of paper are readily available, and the technique is both very flexible in what it can do, and very convenient to use."

Now, researchers grow cells in a Petri dish, creating a thin, two-dimensional layer of cells. If they want to do a better job of mimicking real tissue, they culture the cells in a gel. But because cells in different locations get vastly different amounts of oxygen and food, these cultures fail to mimic real tissues. And studying the cells from different parts of these gels without destroying the 3D culture is tricky.

By growing the cells in a thin layer of gel supported by paper, and then stacking those pieces of paper, the scientists showed they could recreate the benefits of two-dimensional research – where cells receive a uniform amount of oxygen and food -- while also closely mimicking real tissue. In this case, they engineered a 3D tumor on paper that exhibited behaviors similar to a cancer in the body.

Stacking multiple cell-containing sheets also allows researchers to examine the interior of a large cell cluster, either cultured on a dish or grown in vivo, simply by peeling the layers apart, without disturbing the properties of the cells. Isolating cells grown with other 3D culture techniques requires either performing complex laser-assisted surgery on the tumor sections or destroying the architecture of the tissue and then sorting the cells.

Derda said he had the initial insight that led to this study when he heard a colleague complain that he couldn't use paper to filter blood, because the erythrocytes, which give blood their red color, are sometimes trapped in the paper and sometimes go through it. Derda, who developed and used peptide arrays for stem cell research in his Ph.D. work, thought he might be able to use this trapping property for high-throughput screening. When he discussed that insight with Whitesides, the older chemist suggested Derda try stacking the pages instead.

Fellow postdoctoral student Anna Laromaine helped Derda figure out how to clip multiple layers of paper together while submerged in the gel, allowing the first multi-layer cell culture to grow. When he gingerly pulled the sheets of paper apart and analyzed the distribution of cells in different layers, he realized the versatility of paper as a growing medium and its potential to mimic any three-dimensional tissue.

"The best thing about this approach is that it can be used by everyone," Derda said. "Paper is nearly free, it's all over the place and you don't have to know anything other than how to dip."

The work was supported by funds from the Wyss Institute, National Institutes of Health, Vertex Inc., DoD Breast Cancer Innovator Award, the Fulbright-Generalitat de Catalunya, and the American Heart Association.

In addition to Derda, Whitesides and Ingber, the founding director of the Wyss Institute, a faculty member at Harvard's Medical School and its School of Engineering and Applied Sciences, and a researcher at Children's Hospital Boston, the paper's other authors are: Akiko Mammoto and Tadanori Mammoto of Ingber's lab, and Laromaine and Sindy K. Y. Tang of Whitesides' lab.

Reference:

Akiko Mammoto et al. Paper-Supported Three-Dimensional Cell Culture for Tissue-Based Bioassays. Proceedings of the National Academy of Sciences, October 19, 2009


Sunday, October 25, 2009

Scientists Identify Specific Markers That Trigger Aggressiveness Of Liver Cancer

Hepatocellular carcinoma (HCC) or primary liver cancer forms in the epithelial tissue of the liver and is most commonly caused by the hepatitis B virus (HBV) or hepatitis C virus (HCV). In the U.S., the National Cancer Institute (NCI) estimates that 15,000 men and 6,000 women are diagnosed with HCC each year. Worldwide, HCC accounts for 632,000 cases with the highest regions being Western Pacific and Africa according to a 2004 World Health Organization (WHO) report.

Researchers from Taipei Veterans General Hospital investigated the molecular mechanisms of HCC, one of the most common tumors found in Taiwan and largely caused by the high prevalence (15%-20%) of HBV in the country. The study, funded in part by a grant from the National Science Council, is the first to provide a comprehensive profile of multiple Epithelial-Mesenchymal Transition (EMT) markers and to demonstrate that Snail and Twist, but not Slug, are the major inducers of EMT in HCC. Results of the study are published in the November issue of Hepatology, a journal of the American Association for the Study of Liver Diseases.

EMT is critical in the development of invasiveness and metastatic potential of human cancers, and described as process where epithelial cells no longer adhere to one another, taking on fibroblastic properties. The EMT process is initiated by suppression of E-cadherin function through the major EMT regulators (Snail, Slug, and Twist). E-cadherin (calcium dependent adhesion molecules) is a type of protein found in the epithelial cells that ensure tissue cells bind together. When E-cadherin function is lost, cancer is able to progress and metastasize.

Professor Jaw-Ching Wu and colleagues obtained samples of primary HCC with adjacent non-tumorous liver tissues from 123 patients who had hepatic resection surgery between 1990 and 2002 at Taipei Veterans General Hospital. Reduced E-cadherin function was observed in 60.2% of patients. "We found a significant decrease in cancer-free intervals and overall survival for those patients who had a reduction in E-cadherin function," explained Dr. Wu. A downregulated expression of E-cadherin was also associated with large tumor size and multi-nodular tumors.

Results show that co-expression Snail and Twist (transcription factors or proteins that control when genes are switched on or off) indicates the worst prognosis for HCC patients. "Our research is the first to prove that the two proteins (Snail and Twist) work independently, but together promote EMT," noted Dr. Wu.

According to the study, overexpression of Twist is correlated with HCV-related HCC, partially explaining the highly invasive behavior and poor prognosis for patients with this form of liver cancer. Dr Wu added, "Our results provide essential information for determining HCC prognosis in patients and identifies possible new treatments for future HCC management."

Reference

  1. Yang et al. Comprehensive analysis of the independent effect of twist and snail in promoting metastasis of hepatocellular carcinoma. Hepatology, 2009; DOI: 10.1002/hep.23221
  2. Gianluigi Giannelli. The Epithelial Mesenchymal Transition: fact or fiction in cancer? Hepatology;, Published Online: October 29, 2009 DOI: 10.1002/hep.23329