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Noninvasive intravital high-resolution imaging of pancreatic neuroendocrine tumours

Balan, Mirela (författare)
Karolinska Institute
Trusohamn, Marta (författare)
Karolinska Institute
Ning, Frank Chenfei (författare)
Karolinska Institutet,Karolinska Institute
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Jacob, Stefan (författare)
Karolinska Institute,Karolinska University Hospital
Pietras, Kristian (författare)
Lund University,Lunds universitet,Experimentell onkologi,Forskargrupper vid Lunds universitet,Experimental oncology,Lund University Research Groups
Eriksson, Ulf (författare)
Karolinska Institutet,Karolinska Institute
Berggren, Per Olof (författare)
Karolinska Institutet,Karolinska Institute,Karolinska University Hospital
Nyqvist, Daniel (författare)
Karolinska Institutet,Karolinska Institute
visa färre...
 (creator_code:org_t)
2019-10-10
2019
Engelska.
Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 9:1, s. 14636-14636
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Preclinical trials of cancer drugs in animal models are important for drug development. The Rip1Tag2 (RT2) transgenic mouse, a model of pancreatic neuroendocrine tumours (PNET), has provided immense knowledge about PNET biology, although tumour progression occurs in a location inaccessible for real-time monitoring. To overcome this hurdle we have developed a novel platform for intravital 3D imaging of RT2 tumours to facilitate real-time studies of cancer progression. Pre-oncogenic islets retrieved from RT2 mice were implanted into the anterior chamber of the eye (ACE) of host mice, where they engrafted on the iris, recruited blood vessels and showed continuous growth. Noninvasive confocal and two-photon laser-scanning microscopy through the transparent cornea facilitated high-resolution imaging of tumour growth and angiogenesis. RT2 tumours in the ACE expanded up to 8-fold in size and shared hallmarks with tumours developing in situ in the pancreas. Genetically encoded fluorescent reporters enabled high-resolution imaging of stromal cells and tumour cell migration. Sunitinib treatment impaired RT2 tumour angiogenesis and growth, while overexpression of the vascular endothelial growth factor (VEGF)-B increased tumour angiogenesis though tumour growth was impaired. In conclusion, we present a novel platform for intravital high-resolution and 3D imaging of PNET biology and cancer drug assessment.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Biomedicinsk laboratorievetenskap/teknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Biomedical Laboratory Science/Technology (hsv//eng)

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