Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/25727
Title: Vincristine modulates the expression of Ki67 and apoptosis in naturally occurring canine transmissible venereal tumor (TVT)
Authors: Baştan, Ayhan
Baştan, İdil
Darbaz, İsfendiyar
Salar, Seçkin
Karakaş, Kübra
Uludağ Üniversitesi/Veteriner Fakültesi/Jinekoloji ve Doğum Anabilim Dalı.
Uludağ Üniversitesi/Veteriner Fakültesi/Histoloji ve Embriyoloji Anabilim Dalı.
0000-0003-4694-6937
Özalp, Gözde Rabia
Zik, Berrin
Peker, Sabire
Özdemir, Emsal Sinem Salcı
AAH-9810-2021
AAE-3607-2019
23985710500
6507763192
55109615900
55249919300
Keywords: Biotechnology & applied microbiology
Cell biology
Apoptosis
Canine
TVT
Vincristine sulfate
Growth
Regression
Sarcoma
Chemotherapy
Progression
Efficacy
Therapy
Dogs
Cell
Issue Date: Jul-2012
Publisher: Taylor & Francis
Citation: Özalp, G. R. vd. (2012). "Vincristine modulates the expression of Ki67 and apoptosis in naturally occurring canine transmissible venereal tumor (TVT)". Biotechnic & Histochemistry, 87(5), 325-330.
Abstract: We investigated eight adult dogs that were brought to veterinary clinics with a history of transmissible venereal tumors (TVT). Our goal was to demonstrate the occurrence of apoptosis and the cessation of cell proliferation at every phase of scheduled chemotherapy for naturally occurring TVT. Tissue samples were collected immediately after weekly treatments with vincristine sulfate and processed for histological purposes. Sections 5 mu m thick were stained by the TUNEL reaction for apoptosis and immunostained for Ki67 as a proliferation marker. We observed that after vincristine applications, tumor cell proliferation ceased and apoptosis increased. Ki67 HSCORE values were significantly lowered after the first and second treatments with the chemotherapeutic agent compared to controls, whereas TUNEL HSCORE values were significantly higher after two applications of vincristine compared to controls. Our results suggest that scheduled vincristine sulfate applications stabilize the induction of tumor regression by inducing apoptosis and preventing cell proliferation.
URI: https://doi.org/10.3109/10520295.2012.655311
https://www.tandfonline.com/doi/full/10.3109/10520295.2012.655311
http://hdl.handle.net/11452/25727
ISSN: 1052-0295
1473-7760
Appears in Collections:Scopus
Web of Science

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