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Press Release 130/2015

Pancreatic Cancer: CD44 Protein induces Metastases

Peptides Might Help Fighting Pancreatic Tumors/Biologists Studied the CD44v6 Isoform and Discovered Peptides that Inhibit Metastatic Spreading
2015_130_Pankreas-Krebs_-_Protein_CD44_beeinflusst_Metastasen_72dpi
Cells of a pancreatic tumor: Yellow areas show the co-localization of c-Met and CD44v6 proteins. (Photo: ITG/KIT)

Due to their rapid metastatic spread, pancreatic tumors are among the most aggressive types of cancer. Only three to five percent of patients have a survival rate of five years. A team of KIT researchers has now established the basis for new therapeutic approaches. In the Gastroenterology journal they report that in various pancreatic cancer mouse models CD44v6-specific peptides do not only inhibit the spread of tumor cells, but may even lead to the regression of already existing metastases. (DOI 10.1053/j.gastro.2015.10.020).

 

“We think that these peptides have a high potential for tumor therapy, above all for the treatment of pancreatic cancer with its aggressive metastases,” Véronique Orian-Rousseau of the Institute of Toxicology and Genetics (ITG) of KIT says. The CD44v6 protein was discovered in the 1990s by KIT. It acts as a co-receptor for so-called receptor tyrosine kinases, such as MET or VEGFR-2, that depend on CD44 for their activation. These enzymes largely influence the activities of tumor cells. MET accelerates their proliferation, migration, and invasion. VEGFR-2 promotes angiogenesis, i.e. the formation of new blood vessels required to supply the tumor. Hence, they are decisive for the growth and spread of tumor cells.

 

In pre-clinical studies on animals and using various pancreatic cancer models, KIT scientists proved for the first time that the co-receptor function of CD44v6 drives the metastatic spreading. Interestingly, small segments of the CD44v6 protein (called v6pep) turned out to be successful inhibitors of metastasis in animal experiments. The researchers assume that they interfere with the three-dimensional protein structure of CD44v6 and inactivate it in this way. Peptide treatment of tumor-bearing animals led to a reduction of tumor load and to the inhibition of metastasis. Moreover, already existing metastases regressed or disappeared completely: “This is the most remarkable result with respect to pancreatic cancer, the diagnosis of which mostly is possible after the formation of metastases only,” Orian-Rousseau says. In the animal experiments the survival time increased dramatically. The v6pep peptides were found to be much more effective than Crizotinib and Pazopanib, tyrosine kinase inhibitors directed against MET and VEGFR2 respectively. The evaluation of data of patients suffering from pancreatic cancer shows that metastasis and shorter survival times correlate with an increased level of CD44v6 and MET.

 

“This means that we have made an important step forward in basic research that will help the development of anti-cancer drugs,” the scientist explains. Clinical studies that are planned to be made in cooperation with the KIT spinoff “amcure GmbH” in late 2016 will reveal whether the peptides will be effective in human patients.

 

Inhibition of Tumor Growth and Metastasis in Pancreatic Cancer Models by Interference with CD44v6 Signaling, Gastroenterology, Alexandra Matzke-Ogi et al., DOI:10.1053/j.gastro.2015.10.020,
www.sciencedirect.com/science/article/pii/S001650851501519X

 

Karlsruhe Institute of Technology (KIT) pools its three core tasks of research, higher education, and innovation in a mission. With about 9,300 employees and 25,000 students, KIT is one of the big institutions of research and higher education in natural sciences and engineering in Europe.

KIT – The Research University in the Helmholtz Association

sur, 03.11.2015

For further information, please contact:

Kosta Schinarakis
PKM, Themenscout
Tel.: +49 721 608-41956
Fax: +49 721 608-43568
E-Mail:schinarakis@kit.edu
The photo of printing quality may be requested by presseJhz9∂kit edu or phone: +49 721 608-47414. The press release is available as a PDF file.