Strategic Communication and Public Relations

How to prevent the spread of tumor cells via the lymph vessels

No. 66 | 26/10/2020 | by Koh

What role do the lymphatic vessels play in the metastasis of cancer cells? Scientists from the German Cancer Research Center and the Mannheim Medical Faculty of the University of Heidelberg developed a method to investigate this question in mice. The aim of the work was to identify new ways to block the dangerous colonization and spread of tumor cells. The researchers discovered that an antibody against a signaling molecule of the vascular system causes the lymphatic vessels in the tumor to die, suppresses metastasis and thus prolongs the survival of the mice. Based on these findings, approaches may be developed to prevent the dangerous spread of tumor cells. The results have now been published in the journal Cancer Discovery.

Histological image of blood vessels (green) and lymph vessels (orange) in a cross-section of a tumor. Right: Treatment with an angiopoietin-2-blocking antibody leads to the death of the tumor lymph vessels and prevents the spread of tumor cells via the lymph vessel system.
© H. Augustin/DKFZ

Just like healthy tissue, tumors are supplied by two different vascular systems. In addition to blood vessels that supply oxygen and nutrients, the lymph vessels are responsible for transporting cells of the immune system and tissue fluid. The ability of cancer cells to spread through both pathways in the body and form daughter tumors, so-called metastases, has been known for a long time. In this work, the importance of the route via lymphatic vessels and the biological mechanisms involved were investigated for the first time in mice.

Until now, it has been difficult to study the complicated architecture of a tumor and its spread in a living organism. The Heidelberg and Mannheim research team led by Hellmut Augustin has now succeeded in developing a suitable model system, as Nicolas Gengenbacher, first author of the current publication, reports: "The key to this was a direct transplantation of tumor tissue from one mouse to another without prior cell culture. In this model, the natural tissue structure was preserved and the cancerous tumors were able to form functional lymph vessels that were connected to the lymphatic system - a prerequisite for lymphogenic metastasis".

Using these animals, the researchers were able to confirm that cancer cells often migrate via the lymph vessels first into nearby lymph nodes and from there continue to metastasize into vital organs. The surgical removal of the primary tumor enabled the researchers to simulate a disease situation that corresponded to that of a cancer patient after surgery: Daughter tumors and not the primary tumor became crucial for survival.

In their search for ways to prevent the development of metastases, the research team focused on the cells that line the lymph vessels from the inside, the so-called lymph endothelial cells. Endothelial cells control many important properties of the blood and lymph vessels and produce numerous signaling molecules and growth factors. The researchers found that the messenger substance angiopoietin 2 ensures the survival of lymph endothelial cells in tumors. An antibody that blocks angiopoietin-2 caused the lymph vessels in the tumor to selectively die. This interrupted the transport pathways for cancer cells to detach and prevented them from spreading to nearby lymph nodes. As a result, fewer daughter tumors formed in distant organs and the mice survived significantly longer.

Malignant cells often remain in the body after cancer surgery and can be the starting point for a relapse oft he disease. "Surprisingly, we were able to effectively prevent the spread of tumors in the mice even when we blocked angiopoietin-2 only shortly before tumor surgery," says Hellmut Augustin, head of the study. "However, we have only been able to show that angiopoietin-2 blockade has a therapeutic effect within this treatment window in experimental animals. Whether this approach also helps in humans against the spread of tumors must be clarified in further investigations."

Nicolas Gengenbacher, Mahak Singhal, Carolin Mogler, Ling Hai, Laura Milde, Ashik Ahmed Abdul Pari, Eva Besemfelder, Claudine Fricke, Daniel Baumann, Stephanie Gehrs, Jochen Utikal, Moritz Felcht, Junhao Hu, Matthias Schlesner, Rienk Offringa, Sudhakar R. Chintharlapalli, Hellmut G. Augustin: Timed Ang2-targeted therapy 1 identifies the Angiopoietin-Tie pathway as key regulator of fatal lymphogenous metastasis.
Cancer Discovery 2020, DOI: 10.1158/2159-8290.CD-20-0122

A picture is available for download:
https://www.dkfz.de/de/presse/pressemitteilungen/2020/bilder/PM-Gengenbacher-et-al-Image.png 

Picture Caption: Histological image of blood vessels (green) and lymph vessels (orange) in a cross-section of a tumor. Right: Treatment with an angiopoietin-2-blocking antibody leads to the death of the tumor lymph vessels and prevents the spread of tumor cells via the lymph vessel system.

Note on use of images related to press releases
Use is free of charge. The German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ) permits one-time use in the context of reporting about the topic covered in the press release. Images have to be cited as follows: "Source: H. Augustin/DKFZ".
Distribution of images to third parties is not permitted unless prior consent has been obtained from DKFZ's Press Office (phone: ++49-(0)6221 42 2854, E-mail: presse@dkfz.de). Any commercial use is prohibited.

 

The German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ) with its more than 3,000 employees is the largest biomedical research institution in Germany. More than 1,300 scientists at the DKFZ investigate how cancer develops, identify cancer risk factors and search for new strategies to prevent people from developing cancer. They are developing new methods to diagnose tumors more precisely and treat cancer patients more successfully. The DKFZ's Cancer Information Service (KID) provides patients, interested citizens and experts with individual answers to all questions on cancer.

Jointly with partners from the university hospitals, the DKFZ operates the National Center for Tumor Diseases (NCT) in Heidelberg and Dresden, and the Hopp Children's Tumour Center KiTZ in Heidelberg. In the German Consortium for Translational Cancer Research (DKTK), one of the six German Centers for Health Research, the DKFZ maintains translational centers at seven university partner locations. NCT and DKTK sites combine excellent university medicine with the high-profile research of the DKFZ. They contribute to the endeavor of transferring promising approaches from cancer research to the clinic and thus improving the chances of cancer patients.

The DKFZ is 90 percent financed by the Federal Ministry of Education and Research and 10 percent by the state of Baden-Württemberg. The DKFZ is a member of the Helmholtz Association of German Research Centers.

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