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Perivascular Neuropilin-1 expression is an independent marker of improved survival in renal cell carcinoma

Morin, Eric (författare)
Uppsala universitet,Uppsala University,Vaskulärbiologi
Lindskog, Cecilia (författare)
Uppsala universitet,Uppsala University,Institutionen för immunologi, genetik och patologi
Johansson, Martin (författare)
Lund University,Lunds universitet,Klinisk patologi, Malmö,Forskargrupper vid Lunds universitet,LUCC: Lunds universitets cancercentrum,Övriga starka forskningsmiljöer,Clinical pathology, Malmö,Lund University Research Groups,LUCC: Lund University Cancer Centre,Other Strong Research Environments,Department of Laboratory Medicine, Lund University, Lund, Sweden
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Egevad, Lars (författare)
Karolinska Institutet
Sandström, Per (författare)
Karolinska University Hospital,Department of Oncology‐Pathology, Karolinska Institutet, Stockholm, Sweden
Harmenberg, Ulrika (författare)
Karolinska University Hospital,Department of Oncology‐Pathology, Karolinska Institutet, Stockholm, Sweden
Claesson-Welsh, Lena (författare)
Uppsala universitet,Uppsala University,Vaskulärbiologi
Sjöberg, Elin (författare)
Uppsala universitet,Uppsala University,Vaskulärbiologi
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 (creator_code:org_t)
2020-01-29
2020
Engelska 10 s.
Ingår i: Journal of Pathology. - : Wiley. - 0022-3417 .- 1096-9896. ; 250:4, s. 387-396
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Renal cell carcinoma (RCC) treatment has improved in the last decade with the introduction of drugs targeting tumor angiogenesis. However, the 5-year survival of metastatic disease is still only 10–15%. Here, we explored the prognostic significance of compartment-specific expression of Neuropilin 1 (NRP1), a co-receptor for vascular endothelial growth factor (VEGF). NRP1 expression was analyzed in RCC tumor vessels, in perivascular tumor cells, and generally in the tumor cell compartment. Moreover, complex formation between NRP1 and the main VEGF receptor, VEGFR2, was determined. Two RCC tissue microarrays were used; a discovery cohort consisting of 64 patients and a validation cohort of 314 patients. VEGFR2/NRP1 complex formation in cis (on the same cell) and trans (between cells) configurations was determined by in situ proximity ligation assay (PLA), and NRP1 protein expression in three compartments (endothelial cells, perivascular tumor cells, and general tumor cell expression) was determined by immunofluorescent staining. Expression of NRP1 in perivascular tumor cells was explored as a marker for RCC survival in the two RCC cohorts. Results were further validated using a publicly available gene expression dataset of clear cell RCC (ccRCC). We found that VEGFR2/NRP1 trans complexes were detected in 75% of the patient samples. The presence of trans VEGFR2/NRP1 complexes or perivascular NRP1 expression was associated with a reduced tumor vessel density and size. When exploring NRP1 as a biomarker for RCC prognosis, perivascular NRP1 and general tumor cell NRP1 protein expression correlated with improved survival in the two independent cohorts, and significant results were obtained also at the mRNA level using the publicly available ccRCC gene expression dataset. Only perivascular NRP1 expression remained significant in multivariable analysis. Our work shows that perivascular NRP1 expression is an independent marker of improved survival in RCC patients, and reduces tumor vascularization by forming complexes in trans with VEGFR2 in the tumor endothelium.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

in situ proximity ligation assay (PLA)
kidney cancer
Neuropilin
NRP1
renal cell carcinoma (RCC)
trans-complex
VEGF
VEGFR2
renal cell carcinoma

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