• 8/8/2013

Researchers investigate 59 tumor cell lines

Typical protein profile of tumor cells decoded

How does an ordinary somatic cell become cancerous? What are the distinct characteristics of tumor cells that make them divide uncontrollably? Previously, researchers were primarily interested in mutations in DNA, which is the blueprint for proteins. But since proteins are ultimately responsible for converting somatic cells into tumor cells, scientists have now decoded the proteome of 59 tumor cell lines – and have found new ways to explain why cancer drugs do not have the same effect on all patients.

How sensitively do cancer cells react to anti-tumor drugs? The answer lies in the protein patterns of the tumor cell lines.
How sensitively do cancer cells react to anti-tumor drugs? The answer lies in the protein patterns of the tumor cell lines. (Chart: A. Gholami/TUM)

In what is the biggest study of its kind to date, researchers from Technische Universität München (TUM) have identified over 10,000 different proteins in cancer cells. “Nearly all anti-tumor drugs are targeted against cellular proteins,” says Prof. Bernhard Küster, Head of the TUM Chair of Proteomics and Bioanalytics. “Identifying the proteome  the protein portfolio of tumor cells  increases our chances of finding new targets for drugs.”

The scientists investigated 59 tumor cell lines from the US National Cancer Institute. The “NCI-60” cell lines represent the most common tumor diseases in nine tissues (e.g. brain, breast, bowels, skin, blood). Cancer researchers in all parts of the world use them in their experiments. TUM bioinformatics expert Dr. Amin Gholami elaborates: “Before now, there was little knowledge on the proteome of the NCI-60 cell lines. But it is proteins that make the difference between a healthy cell and a tumor cell.” 

Proteins in tumor cells: a lot in common – and huge diversity

The scientists found over 10,000 different proteins in the NCI-60 cell lines. More than 5,000 of them are present in varying abundance in tumor cell lines of all types of tissue. “We can assume that this is the core proteome of cancer,” comments Küster. However, the researchers also found some clearly distinguishable protein profiles between the tumor cells of different tissues – a clear indication that the tumor cells possess typical characteristics of healthy cells of the same tissue. 

375 of the 10,000 or so proteins belong to the kinase group. These proteins are responsible for transmitting signals which cells use to control their metabolic reactions, their division, or their communication with other cells in the tissue, for example. Tumor biologist Dr. Zhixiang Wu explains the wide range of different kinases in the NCI-60 cell line panel: “Unlike healthy cells, tumor cells are open to many signaling pathways in order to activate their division and ensure their survival.”  

Küster adds: “The kinases play a part in the continuous reproduction process of tumor cells. The wide variety of kinases shows how different these mechanisms are in human cancer diseases. This is an important discovery for personalized medicine.”

Effectiveness of drugs dependent on protein pattern

In another first, TUM researchers were able to prove that the protein pattern of the cells determines the effectiveness of cancer drugs. “We investigated how the cell lines react to 108 different cancer drugs and found that there are indeed proteins that indicate whether a cell will respond to certain therapeutic agents – or whether it will be resistant to the drug,” explains Dr. Hannes Hahne, TUM expert in mass spectrometry techniques. As an example, he mentions the 14-3-3 zeta/delta protein, which is suspected of mediating resistance against cancer drugs. 

The NCI-60 proteome database can be consulted by scientists. “We want to play our part to advance proteome research in the area of cancer diseases,” concludes Küster. “Our next project will involve investigating the proteome of the ‘Cancer Cell Line Encyclopedia’, which pharmaceutical firms use to test new anti-cancer drugs.”

Global proteome analysis of the NCI-60 cell line panel; Amin Moghaddas Gholami, Hannes Hahne, Zhixiang Wu, Florian Johann Auer, Chen Meng, Mathias Wilhelm and Bernhard Kuster, Cell Reports Volume 4, 2013, doi: 10.1016/j.celrep.2013.07.018


Technische Universität München
Chair of Proteomics and Bioanalytics
Prof. Dr. Bernhard Küster
T: +49 8161 71-5697
E: kusterspam prevention@tum.de
W: www.weihenstephan.de/bt/

Technical University of Munich

Corporate Communications Center

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