Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/27331
Title: The expressions of pAkt and PTEN in lung cancer patients 24 hours after the cisplatin-based chemotherapy: A prospective pilot study
Other Titles: Akciǧer kanserli hastalarda sisplatin-Bazlı tedaviden 24 saat sonra pAkt ve PTEN ekspresyonları: Prospektif pilot çalışma
Authors: Yağcı, Artay
Sevimli, Alper
Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Anabilim Dalı.
Uludağ Üniversitesi/Veterinerlik Fakültesi/Histoloji ve Embriyoloji Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Biyokimya Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/TB ve Göğüs Hastalıkları Anabilim Dalı.
0000-0002-6729-7908
0000-0003-0463-6818
Ulukaya, Engin
Oral, Arzu Yılmaztepe
Zık, Berrin
Arı, Ferda
Akgöz, Semra
Ursavaş, Ahmet
Bayer, Sibel
K-5792-2018
AAI-3169-2021
AAH-9810-2021
AAG-7012-2021
A-5841-2017
6602927353
23091316500
6507763192
24376085300
14061863400
8329319900
57215362032
Keywords: Oncology
Lung Cancer
pAkt
PTEN
Cisplatin
Chemotherapy
Protein-kinase-b
Prognostic-significance
Akt activation
Breast-cancer
Cell-death
Apoptosis
Tumors
Mechanisms
Survival
Gene
Akciğer kanseri
Kemoterapi
Sisplatin
Issue Date: 2011
Publisher: Akad Doktorlar Yayınevi
Citation: Ulukaya, E. vd. (2011). "The expressions of pAkt and PTEN in lung cancer patients 24 hours after the cisplatin-based chemotherapy: A prospective pilot study". UHOD - Uluslararasi Hematoloji-Onkoloji Dergisi, 21(1), 26-33.
Abstract: Akt/PKB is a protooncogen while PTEN is a tumor suppressor gene. Their expressions are of immense importance in the development of lung cancer. However, little is known about their relations to anti-cancer treatments. Therefore, we aimed to elucidate how are these parameters affected by the treatment. Expression of phosphorylated Akt (pAkt) and PTEN have been analysed on tissues of 32 patients (stage Ill and IV) with lung cancer. In addition, the expression of these variables in 14 out of 32 patients have furtherly been analysed in terms of their response to cisplatin-based chemotherapy in vivo. Prior to and 24 h after the treatment, tumor tissues were obtained via broncoscopy and then evaluated immunohistochemically by indirect streptavidin-biotin peroxidase method. Immunoreactivity for pAkt was detected in 29 of 32 cases (91%). pAkt was observed to localize in the nucleus of positively stained cells. However, PTEN expression was found in 27 of 32 cases (84%). In contrast to the localization of pAkt that is nucleus, PTEN was however localized in the cytoplasm of positively stained cells. pAkt and PTEN expression levels of 14 post-chemotherapy patients were compared to those before chemotherapy. There was no statistically significant differences (p>0.05). Although these results do not imply any possible roles of pAkt or PTEN in the late stage lung cancer patients as a biomarker for the prediction of early response to treatment in vivo, this conclusion needs to be analyzed further at later time points in a larger cohort.
URI: https://doi.org/10.4999/uhod.09105
http://www.uhod.org/pdf/PDF_451.pdf
http://hdl.handle.net/11452/27331
ISSN: 1306-133X
Appears in Collections:Web of Science

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