Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Mhaidat, Nizar M.a; * | Alzoubi, Karem H.a | Almomani, Nabeelaa | Khabour, Omar F.b; c
Affiliations: [a] Department of Clinical Pharmacy, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid, Jordan | [b] Department of Laboratory Medical Sciences, Faculty of Applied Medical Sciences, Jordan University of Science and Technology, Irbid, Jordan | [c] Department of Biology, Faculty of Science, Taibah University, Almadina, Saudi Arabia
Correspondence: [*] Corresponding author: Nizar M. Mhaidat, Department of Clinical Pharmacy, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid 22110, Jordan. Tel.: +962 2 720100; Fax: +962 2 7201075; E-mail: [email protected].
Abstract: Background:Colorectal cancer (CRC) is an important health problem all over the world. A great improvement in the screening and early detection of CRC has been achieved. However, a new molecular prognostic marker is largely required. Glucose regulated protein 78-kDa (GRP78) is the central regulator of the endoplasmic reticulum (ER) and has an important role in the proliferation, differentiation and resistance to chemotherapy in cancer cells. Objective:The aim of the present study was to investigate the impact of elevated level of GRP78 on CRC prognosis and chemosensitivity. Methods:Sixty eight CRC tissue samples were collected and protein expression of GRP78 was evaluated using immunohistochemistry. The clinicopathological factors of the patients were correlated with GRP78 level. Results:GRP78 expression increased with the progression from early to advanced CRC stages. In addition, GRP78 level was increased with the progression from early T1-2 to late T3-4 tumor localization (p< 0.05). Moreover, a significant association was found between GRP78 expression and response to chemotherapy (p< 0.05). Association between GRP78 expression and patient’s clinical characteristics including lymph node involvement and metastasis was not significant. Conclusions:Results suggest the possibility to use GRP78 as a biomarker for progression of CRC and its chemosensitivity to therapy.
Keywords: Colorectal cancer, GRP78, Chemotherapy, Apoptosis
DOI: 10.3233/CBM-140454
Journal: Cancer Biomarkers, vol. 15, no. 2, pp. 197-203, 2015
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
[email protected]
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office [email protected]
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
如果您在出版方面需要帮助或有任何建, 件至: [email protected]