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- Challenges and Chances: A Review of the 1st Stem Cell Community Day
- Summertime, and the Livin’ Is Easy…
- Follow-on-Biologics – More than Simple Generics
- Bacteria Versus Body Cells: A 1:1 Tie
- Behind the Crime Scene: How Biological Traces Can Help to Convict Offenders
- Every 3 Seconds Someone in the World Is Affected by Alzheimer's
- HIV – It’s Still Not Under Control…
- How Many Will Be Convicted This Time?
- Malaria – the Battle is Not Lost
- Physicians on Standby: The Annual Flu Season Can Be Serious
- At the Forefront in Fighting Cancer
- Molecular Motors: Think Small and yet Smaller Again…
- Liquid Biopsy: Novel Methods May Ease Cancer Detection and Therapy
- They Are Invisible, Sneaky and Disgusting – But Today It’s Their Special Day!
- How Many Cells Are in Your Body? Probably More Than You Think!
- What You Need to Know about Antibiotic Resistance – Findings, Facts and Good Intentions
- Why Do Old Men Have Big Ears?
- The Condemned Live Longer: A Potential Paradigm Shift in Genetics
- From Research to Commerce
- Chronobiology – How the Cold Seasons Influence Our Biorhythms
- Taskforce Microbots: Targeted Treatment from Inside the Body
- Eyes on Cancer Therapy
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- 2007年の受賞者:ポルトガルのオエイラスにあるInstituto Gulbenkian de CiênciaのMónica Bettencourt-Dias博士
2007 Award Winner Dr. Mónica Bettencourt-Dias Instituto Gulbenkian de Ciência, Oeiras, Portugal
Appointment at time of winning the Award
Group Leader, Instituto Gulbenkian de Ciência, Oeiras, Portugal
Abstract
Our research is focused on the regulation of cell proliferation, with an emphasis on the centrosome, the primary microtubule organizing centre in animal cells. Problems with centrosomes and its core structures, the centrioles, are associated with a variety of human diseases, from cancer to infertility. The formation of these structures is highly regulated. They duplicate once every cell cycle, with one centriole, the “daughter”, forming close to an already existing one, the “mother”, so that their number remains stable. To provide new perspectives on cell proliferation we screened by RNAi all the protein kinases from fruit flies. Amongst several novel players, we identified SAK/PLK4, a kinase implicated in tumourigenesis. We showed in flies and humans that SAK/PLK4 is essential for centriole duplication. Strikingly, SAK/PLK4 can trigger centriole formation in the absence of a mother, i.e, de novo, showing the mother centriole is not a bona-fide “template” in daughter formation. Instead, it is a platform for recruitment of regulatory molecules, such as SAK/PLK4, hence triggering the assembly of daughter centrioles close by. This work suggests misregulation of centriole duplication regulators may generate some of the centrosome abnormalities observed in cancer. In that case, those molecules may be used in the diagnostic, prognostic and as targets in cancer treatment.
Group Leader, Instituto Gulbenkian de Ciência, Oeiras, Portugal
Abstract
Our research is focused on the regulation of cell proliferation, with an emphasis on the centrosome, the primary microtubule organizing centre in animal cells. Problems with centrosomes and its core structures, the centrioles, are associated with a variety of human diseases, from cancer to infertility. The formation of these structures is highly regulated. They duplicate once every cell cycle, with one centriole, the “daughter”, forming close to an already existing one, the “mother”, so that their number remains stable. To provide new perspectives on cell proliferation we screened by RNAi all the protein kinases from fruit flies. Amongst several novel players, we identified SAK/PLK4, a kinase implicated in tumourigenesis. We showed in flies and humans that SAK/PLK4 is essential for centriole duplication. Strikingly, SAK/PLK4 can trigger centriole formation in the absence of a mother, i.e, de novo, showing the mother centriole is not a bona-fide “template” in daughter formation. Instead, it is a platform for recruitment of regulatory molecules, such as SAK/PLK4, hence triggering the assembly of daughter centrioles close by. This work suggests misregulation of centriole duplication regulators may generate some of the centrosome abnormalities observed in cancer. In that case, those molecules may be used in the diagnostic, prognostic and as targets in cancer treatment.
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