کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2151529 | 1090000 | 2011 | 15 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Androgen Depletion Induces Senescence in Prostate Cancer Cells through Down-regulation of Skp2
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کلمات کلیدی
ADTAIPCS-phase kinase-associated protein 2Skp2IGFBP3NEDSASPIL-8SA-β-galsenescence-associated β-galactosidase - β-گالاکتوزیداز وابسته به پیریInterleukin-8 - اینترلوکین -8Neuroendocrine differentiation - تمایز نوروندوکرینEMT - تکنسین فوریتهای پزشکیADT, Androgen deprivation therapy - درمان محرومیت از آندروژنAndrogen-independent prostate cancer - سرطان پروستات مستقل از آندروژنSenescence-associated secretory phenotype - فنوتیپ ترشحی مرتبط با سن زاییInsulin-like growth factor binding protein 3 - پروتئین اتصال دهنده فاکتور رشد مانند انسولین 3epithelial-to-mesenchymal transition - گذار اپیتلیال به مزانشیمالAndrogen Receptor - گیرنده آندروژنی
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
تحقیقات سرطان
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Although the induction of senescence in cancer cells is a potent mechanism of tumor suppression, senescent cells remain metabolically active and may secrete a broad spectrum of factors that promote tumorigenicity in neighboring malignant cells. Here we show that androgen deprivation therapy (ADT), a widely used treatment for advanced prostate cancer, induces a senescence-associated secretory phenotype in prostate cancer epithelial cells, indicated by increases in senescence-associated β-galactosidase activity, heterochromatin protein 1β foci, and expression of cathepsin B and insulin-like growth factor binding protein 3. Interestingly, ADT also induced high levels of vimentin expression in prostate cancer cell lines in vitro and in human prostate tumors in vivo. The induction of the senescence-associated secretory phenotype by androgen depletion was mediated, at least in part, by down-regulation of S-phase kinase-associated protein 2, whereas the neuroendocrine differentiation of prostate cancer cells was under separate control. These data demonstrate a previously unrecognized link between inhibition of androgen receptor signaling, down-regulation of S-phase kinase-associated protein 2, and the appearance of secretory, tumor-promoting senescent cells in prostate tumors. We propose that ADT may contribute to the development of androgen-independent prostate cancer through modulation of the tissue microenvironment by senescent cells.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neoplasia - Volume 13, Issue 6, June 2011, Pages 526-536, IN10-IN13
Journal: Neoplasia - Volume 13, Issue 6, June 2011, Pages 526-536, IN10-IN13
نویسندگان
Zuzana Pernicová, Eva Slabáková, Gvantsa Kharaishvili, Jan Bouchal, Milan Král, Zuzana Kunická, Miroslav Machala, Alois KozubÃk, Karel SouÄcek,