'If Hamlet give the first or second hit': The development of Burkitt's lymphoma

Public release date: 8-Nov-2011
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Contact: Prof Veronika Sexl
veronika.sexl@vetmeduni.ac.at
43-125-077-2910
University of Veterinary Medicine -- Vienna

The human c-myc gene encodes a transcription factor (MYC) involved in the regulation of a vast number of other genes it has been estimated that the transcription of about one in six genes is somehow under the control of MYC. Perhaps because of MYC's wide range of targets, mutations of the c-myc gene are frequently associated with a variety of tumours, not only with Burkitt's lymphoma. Mutations that lead to excessive amounts of the MYC protein are particularly threatening.

It has long been known that Burkitt's lymphoma only develops when MYC is mutated or overexpressed, although experiments in mice have shown that some animals live quite happily and healthily with higher levels of the MYC protein. This observation is consistent with the "second hit" model for the origin of cancer: as well as a change to c-myc, a second gene must also be disturbed before disease is initiated. In the case of lymphomas, the second hit is often in the p53 or the Bcl2 gene. Loss of p53 or increased amounts of the BCL2 protein are both associated with lymphoma. But how does the course of the disease relate to the nature of the second hit?

This question has now been investigated by Sexl's and Stoiber's groups. Using a mouse model of human lymphoma, the scientists compared the effects on the immune system of deleting the p53 gene or over-activating the Bcl2 gene, or both. The results were dramatic. If the p53 gene was mutated, the resulting tumours were no longer recognized and killed by the mouse's immune system. In other words, such tumours escaped the mouse's normal "surveillance" mechanism and went on to cause full-blown lymphoma. On the other hand, if instead the Bcl2 gene was overexpressed (to produce more BCL2 protein), the mouse's immune system could recognize and attack the tumour cells, thereby slowing or preventing cancer development. If both the p53 and the Bcl2 genes were affected, immune recognition remained efficient, in other words the Bcl2 effect is dominant.

The results show for the first time that the nature of the "second hit" determines whether the animals are able to mount an immune response against the developing lymphoma. Interestingly, Sexl's collaboration partner Ulrich Jger from the Medical University of Vienna has obtained preliminary data from human patients that are consistent with the results in mice. The collaboration shows once again the value of comparative medicine in understanding the progression of human diseases.

The findings have extremely important consequences for tumour therapy in humans. First, because of the association of high BCL2 levels with tumour development, a number of pharmaceutical companies are currently developing BCL2 inhibitors for use in cancer therapy. As Sexl points out, though, "The inhibitors may have the unwanted effect of preventing the natural immune reaction. It will be important to evaluate the consequences of BCL2 inhibition carefully taking the host immune system fully into account to ensure that the drugs have no harmful side-effects." Secondly, the results may potentially shape future immunotherapeutic approaches, as whether a tumour overexpresses Bcl2 or does not express p53 clearly has a dramatic influence on the course of disease.

###

The paper, "The cooperating mutation or 'second hit'" determines the immunologic visibility toward MYC-induced murine lymphomas," by Christian Schuster, Angelika Berger, Maria A. Hoelzl, Eva M . Putz, Anna Frenzel, Olivia Simma, Nadine Moritz, Andrea Hoelbl, Boris Kovacic, Michael Freissmuth, Mathias Mller, Andreas Villunger, Leonard Mllauer, Ana-lris Schmatz, Berthold Streubel, Edit Porpaczy, Ulrich Jger, Dagma Stoiber and Veronika Sexl is published in the current issue of the journal Blood (2011, 118(17):4635-45). The work was performed in close collaboration with other groups at Vetmeduni Vienna and at the Medical University of Vienna and with the group of Andreas Villunger at the Innsbruck Medical University.

Abstract of the scientific article online: http://bloodjournal.hematologylibrary.org/content/early/2011/08/30/blood-2010-10-313098.short

About the Vienna University of Veterinary Medicine

The University of Veterinary Medicine, Vienna is the only academic and research institution in Austria that focuses on the veterinary sciences. About 1000 employees and 2300 students work on the campus in the north of Vienna, which also houses the animal hospital and various spin-off-companies.

http://www.vetmeduni.ac.at

Scientific contact:

Prof Veronika Sexl, E Veronika.Sexl@vetmeduni.ac.at, T 43-1-25077- 2910

Released by:

Klaus Wassermann, E Klaus.Wassermann@vetmeduni.ac.at, T 43-1-25077-1153

---

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AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.

Public release date: 8-Nov-2011
[ | E-mail | Share ]

Contact: Prof Veronika Sexl
veronika.sexl@vetmeduni.ac.at
43-125-077-2910
University of Veterinary Medicine -- Vienna

The human c-myc gene encodes a transcription factor (MYC) involved in the regulation of a vast number of other genes it has been estimated that the transcription of about one in six genes is somehow under the control of MYC. Perhaps because of MYC's wide range of targets, mutations of the c-myc gene are frequently associated with a variety of tumours, not only with Burkitt's lymphoma. Mutations that lead to excessive amounts of the MYC protein are particularly threatening.

It has long been known that Burkitt's lymphoma only develops when MYC is mutated or overexpressed, although experiments in mice have shown that some animals live quite happily and healthily with higher levels of the MYC protein. This observation is consistent with the "second hit" model for the origin of cancer: as well as a change to c-myc, a second gene must also be disturbed before disease is initiated. In the case of lymphomas, the second hit is often in the p53 or the Bcl2 gene. Loss of p53 or increased amounts of the BCL2 protein are both associated with lymphoma. But how does the course of the disease relate to the nature of the second hit?

This question has now been investigated by Sexl's and Stoiber's groups. Using a mouse model of human lymphoma, the scientists compared the effects on the immune system of deleting the p53 gene or over-activating the Bcl2 gene, or both. The results were dramatic. If the p53 gene was mutated, the resulting tumours were no longer recognized and killed by the mouse's immune system. In other words, such tumours escaped the mouse's normal "surveillance" mechanism and went on to cause full-blown lymphoma. On the other hand, if instead the Bcl2 gene was overexpressed (to produce more BCL2 protein), the mouse's immune system could recognize and attack the tumour cells, thereby slowing or preventing cancer development. If both the p53 and the Bcl2 genes were affected, immune recognition remained efficient, in other words the Bcl2 effect is dominant.

The results show for the first time that the nature of the "second hit" determines whether the animals are able to mount an immune response against the developing lymphoma. Interestingly, Sexl's collaboration partner Ulrich Jger from the Medical University of Vienna has obtained preliminary data from human patients that are consistent with the results in mice. The collaboration shows once again the value of comparative medicine in understanding the progression of human diseases.

The findings have extremely important consequences for tumour therapy in humans. First, because of the association of high BCL2 levels with tumour development, a number of pharmaceutical companies are currently developing BCL2 inhibitors for use in cancer therapy. As Sexl points out, though, "The inhibitors may have the unwanted effect of preventing the natural immune reaction. It will be important to evaluate the consequences of BCL2 inhibition carefully taking the host immune system fully into account to ensure that the drugs have no harmful side-effects." Secondly, the results may potentially shape future immunotherapeutic approaches, as whether a tumour overexpresses Bcl2 or does not express p53 clearly has a dramatic influence on the course of disease.

###

The paper, "The cooperating mutation or 'second hit'" determines the immunologic visibility toward MYC-induced murine lymphomas," by Christian Schuster, Angelika Berger, Maria A. Hoelzl, Eva M . Putz, Anna Frenzel, Olivia Simma, Nadine Moritz, Andrea Hoelbl, Boris Kovacic, Michael Freissmuth, Mathias Mller, Andreas Villunger, Leonard Mllauer, Ana-lris Schmatz, Berthold Streubel, Edit Porpaczy, Ulrich Jger, Dagma Stoiber and Veronika Sexl is published in the current issue of the journal Blood (2011, 118(17):4635-45). The work was performed in close collaboration with other groups at Vetmeduni Vienna and at the Medical University of Vienna and with the group of Andreas Villunger at the Innsbruck Medical University.

Abstract of the scientific article online: http://bloodjournal.hematologylibrary.org/content/early/2011/08/30/blood-2010-10-313098.short

About the Vienna University of Veterinary Medicine

The University of Veterinary Medicine, Vienna is the only academic and research institution in Austria that focuses on the veterinary sciences. About 1000 employees and 2300 students work on the campus in the north of Vienna, which also houses the animal hospital and various spin-off-companies.

http://www.vetmeduni.ac.at

Scientific contact:

Prof Veronika Sexl, E Veronika.Sexl@vetmeduni.ac.at, T 43-1-25077- 2910

Released by:

Klaus Wassermann, E Klaus.Wassermann@vetmeduni.ac.at, T 43-1-25077-1153

---

[ | E-mail | Share ]

?

AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.

Source: http://www.eurekalert.org/pub_releases/2011-11/uovm-hg110811.php

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