Selenium-based Experimental Therapeutics
PhD, (Dr sc nat ETH ), Cell Biology/Biochemistry, Swiss Federal Institute of Technology, Zurich, 1976
MS, (Dipl Natw ETH ), Developmental Biology/Biochemistry, Swiss Federal Institute of Technology, Zurich, 1971
1) Development of second-generation merocyanine photosensitizers with improved antineoplastic, antiviral, and anti-protozoan activities. Of particular interest are selone analogs that are characterized by extremely high singlet oxygen quantum yields and the photochemical generation of cytotoxic photoproducts. One merocyanine-based application has made the transition from bench to clinic and is showing promising results in a phase I/II trial in adult patients with high-risk acute myelogenous leukemia.
2) Proteinated subnanoparticles of elemental selenium as a novel class of anti-cancer agents. When selenomerocyanine dyes are exposed to light in the presence of oxygen, they generate subnanoparticles of elemental selenium that combine with serum albumin or lipoproteins to form conjugates that are highly cytotoxic to tumor cells but well tolerated by normal cells. A 1-hour exposure to micromolar concentrations of proteinated selenium is sufficient to reduce clonogenic tumor cells by ≥5 orders of magnitude while preserving virtually all normal pluripotent hematopoietic stem cells.
Figure 1: Photochemical generation of proteinated subnanoparticles of elemental selenium and their effects on leukemia and normal hematopoietic stem cells. The protein component acts as a Trojan horse that exploits the enhanced capacity of tumor cells to bind and internalize serum albumin and lipoproteins. The cytotoxic entity (elemental selenium) is preferentially delivered to tumor cells as part of a physiological process.
3) High-dose selenium for the mitigation of therapy-induced toxicities. This project grew out of an effort to develop medical countermeasures against radiation injuries caused by nuclear accidents or acts of radiological terrorism. We could show that very high (supranutritional) doses of dietary selenium are surprisingly effective at reducing radiation injury to kidney, liver, heart, and lung even if the intervention is initiated after radiation exposure. We are now in the process of extending this approach to the mitigation of therapy-induced toxicities in animal models of radiation- and chemotherapy.
(Traul DL, Sieber F.) J Photochem Photobiol B. 2015 Dec;153:153-63.
(Daziano JP, Günther WH, Krieg M, Tsujino I, Miyagi K, Anderson GS, Sampson RW, Ostrowski MD, Muir SA, Bula RJ, Sieber F.) Photochem Photobiol. 2012 Mar-Apr;88(2):448-60.
(Sieber F, Muir SA, Cohen EP, Fish BL, Mäder M, Schock AM, Althouse BJ, Moulder JE.) Radiat Res. 2011 Sep;176(3):366-74.
(Čunderlíková B, Vasovič V, Sieber F, Furre T, Borgen E, Nesland JM, Peng Q.) Bone Marrow Transplant. 2011 Aug;46(8):1118-27.
(Čunderlíková B, Vasovič V, Sieber F, Furre T, Nesland JM, Peng Q.) Bone Marrow Transplant. 2010 Oct;45(10):1553-61.
(Sieber F, Muir SA, Cohen EP, North PE, Fish BL, Irving AA, Mäder M, Moulder JE.) Radiat Res. 2009 Mar;171(3):368-73.
(Tsujino I, Miyagi K, Sampson RW, Sieber F.) Photochem Photobiol. 2006 Mar-Apr;82(2):458-65.
(Sieber F, Daziano JP, Günther WH, Krieg M, Miyagi K, Sampson RW, Ostrowski MD, Anderson GS, Tsujino I, Bula RJ.) Phosphorus Sulfur Silicon Relat Elem. 2005;180(3-4):647-657.
(Miyagi K, Sampson RW, Sieber-Blum M, Sieber F.) J Photochem Photobiol B. 2003 Jul;70(3):133-44.
Preferential inactivation of paediatric solid tumour cells by sequential exposure to Merocyanine 540-mediated photodynamic therapy and Edelfosine: implications for the ex vivo purging of autologous haematopoietic stem cell grafts.
(Anderson GS, Tsujino I, Miyagi K, Sampson R, Sieber F.) J Photochem Photobiol B. 2003 Feb;69(2):87-95.
(Anderson GS, Miyagi K, Sampson RW, Sieber F.) J Photochem Photobiol B. 2002 Nov;68(2-3):101-8.
(Tsujino I, Anderson GS, Sieber F.) Photochem Photobiol. 2001 Feb;73(2):191-8.