Pancreatic Cancer: ‘Flexibility of Cancer Cells Determining the Area of Metastases.’

A research team at the Technical University of Munich (TUM) has discovered that, pancreatic cancer often spreads and metastasizes in the liver or lungs. The prognosis is said to be better for patients with metastases in the lungs. However, the organ that is more likely to be affected depends on the cancer cells’ ability to alter their characteristics and shape.
Cells in a tissue or tumor establish contacts with other cells and assume a scale-like appearance. Such cells modify their metabolism and detach themselves from the cluster of cells making up the tumor. As a result, they become long and thin, which allows them to enter nearby blood vessels, using them as a transport route to reach other organs and proliferate in tissue there.
The cells then must transform themselves once again, in order to re-establish contacts with other cells. Not all cancer cells possess flexibility, technically known as plasticity.

Dr. Maximilian Reichert, lead author of the new study and research group leader in the Internal Medicine Unit II of TUM University Hospital Klinikum rechts der Isar, discovered this phenomena and its consequences, mainly for pancreatic cancer. The study’s findings were published in the journal Developmental Cell.

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  Metastases in Liver or lungs – what is the decisive factor?

  
  Reichert explained that, through this research, they were able to show that the spread of pancreatic cancer to the liver depends on the plasticity of the cancer cells. If the cells are unable to establish cell-to-cell contacts, they are passively flushed into the lungs by the bloodstream, where they become lodged. “This course of the disease is more favorable for patients, because lung tumors are easier to control.” He added.
  The plasticity of a cancer cell depends crucially on the presence of a cell adhesion molecule: the protein E-cadherin. It is found on the cell surface, responsible for cell-to-cell contacts. Using a mouse model, the research team discovered that, the absence of E-cadherin results in pancreatic cancer cells spreading to the lungs and not to the liver.

When the protein was present and functional, the cancer cells were also able to invade the liver. Researchers believed that, the cancer cells are able to take hold and colonize in liver tissue, due to close cell-to-cell contacts established with the help of E-cadherin. By altering the presence of E-cadherin, the research team was able to control the metastasis process in mice.

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  Epigenetic factors?

  
  The research team also discovered that, these mechanisms are evidently controlled in the tumor by epigenetic programs. In the process, the genetic material (DNA) itself is not altered. Instead, chemical factors determine how strongly or weakly a section of DNA is read.
  
  Together with colleagues at Klinikum rechts der Isar, the team led by Maximilian Reichert plans to investigate whether these epigenetic programs can be inhibited or are suitable targets for treatment. “The more we understand about the formation of metastases, the better we’ll be able to influence the process. This is particularly important in the case of pancreatic cancer, because nearly all pancreatic cancer patients die as a result of metastases,” Reichert added.