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Cellular physiology and biochemistry, 2013-01, Vol.32 (4), p.1117-1123
2013
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Autor(en) / Beteiligte
Titel
Downregulation of Clusterin Expression in Human Testicular Seminoma
Ist Teil von
  • Cellular physiology and biochemistry, 2013-01, Vol.32 (4), p.1117-1123
Ort / Verlag
Basel, Switzerland: Cell Physiol Biochem Press GmbH & Co KG
Erscheinungsjahr
2013
Quelle
Free E-Journal (出版社公開部分のみ)
Beschreibungen/Notizen
  • Background: Clusterin, a heterodimeric glycoprotein of approximately 80 kDa, exists extensively in human body fluids. The abnormal expression of clusterin is closely related to the occurrence, progression, and prognosis of tumors. Up to now, few studies have focused on clusterin in human testicular cancer. This study describes an extensive exploration of the presence and expression of clusterin in testicular seminoma. Methods: Tumor tissues and normal testis tissues were collected from 13 patients with testicular seminoma and 16 patients undergoing surgical castration for prostate cancer. Real-time polymerase chain reaction (PCR) was performed to detect the expression difference of clusterin mRNA between testicular seminoma and normal testis. Western blot and immunohistochemical analysis were performed to detect the presence and expression difference of clusterin protein between two groups. Results: Real-time PCR showed the expression of clusterin mRNA in testicular seminoma to be significantly lower than in normal testis (only 13% relative quantification). Western blot analysis indicated marked reductions in the expression of clusterin protein in testicular seminoma. Similar results were observed upon immunohistochemical analysis. Conclusion: In testicular seminoma and normal testis, clusterin exists in its heterodimeric secretory isoform. Clusterin expression is significantly lower in testicular seminoma than in normal testis. This is the first comprehensive study of the presence and expression of clusterin in human testicular cancer.
Sprache
Englisch
Identifikatoren
ISSN: 1015-8987
eISSN: 1421-9778
DOI: 10.1159/000354511
Titel-ID: cdi_doaj_primary_oai_doaj_org_article_1bb898ba795a4439a15f11a7cf35191c

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