scholarly journals Relationship Between Non-small Cell Lung Cancer FDG Uptake at PET, Tumor Histology, and Ki-67 Proliferation Index

2008 ◽  
Vol 3 (9) ◽  
pp. 971-978 ◽  
Author(s):  
Hubert Vesselle ◽  
Alexander Salskov ◽  
Eric Turcotte ◽  
Linda Wiens ◽  
Rodney Schmidt ◽  
...  
2013 ◽  
Vol 31 (15_suppl) ◽  
pp. e22108-e22108
Author(s):  
Kazuhito Nii ◽  
Dage Liu ◽  
Yoshimasa Tokunaga ◽  
Xia Zhang ◽  
Shinya Ishikawa ◽  
...  

e22108 Background: GPR87 is a member of G-protein-coupled receptors (GPCRs). Recently, GPR87 was suggested to contribute to the viability of human tumor cells, and the overexpression of GPR87 mRNA was found in many malignant tumors including lung cancer. However, the clinical significance of GPR87 expression in non-small cell lung cancer (NSCLC) has not been well studied. Methods: 127 NSCLC patients who underwent surgery from 1999 to 2004 were investigated. There were 59 adenocarcinomas, 55 squamous cell carcinomas and 13 others. The intratumoral expression of GPR87 was evaluated by immunohistochemistry. The Ki-67 proliferation index was also evaluated. Results: A tumor-specific expression of GPR87 was found in NSCLC in comparison with the surrounding normal tissue. Fifty-nine tumors (46.5%) were found to be high-GPR87 tumors. The high-GPR87 tumors were more frequently found in squamous cell carcinoma than in adenocarcinoma (60.0% versus 37.3%, p=0.02). Regarding the tumor proliferation, the Ki-67 index was significantly higher in high-GPR87 tumors than in low-GPR87 tumors (p=0.04). There was a tendency that the overall survival was worse in patients with high-GPR87 tumors than in low-GPR87 tumors (p=0.22). For the patients with adenocarcinoma, the overall survival was significantly worse in patients with high-GPR87 tumors than in low-GPR87 tumors (p=0.04). Conclusions: GPR87 expression may become a poor prognostic predictor for patient with NSCLC, especially for those with adenocarcinoma. GPR87 may contribute to the cell viability by promoting cell proliferation, has a potential to become a novel therapeutic target for cancer treatment.


2017 ◽  
Vol 12 (1) ◽  
Author(s):  
Naoya Ishibashi ◽  
Toshiya Maebayashi ◽  
Takuya Aizawa ◽  
Masakuni Sakaguchi ◽  
Haruna Nishimaki ◽  
...  

2007 ◽  
Vol 34 (10) ◽  
pp. 1610-1616 ◽  
Author(s):  
Yuka Yamamoto ◽  
Yoshihiro Nishiyama ◽  
Shinya Ishikawa ◽  
Jun Nakano ◽  
Sung Soo Chang ◽  
...  

Author(s):  
Seda Beyhan Sagmen ◽  
Coskun Dogan ◽  
Sevda Comert ◽  
Nesrin Kiral ◽  
Elif Torun Parmaksiz ◽  
...  

2007 ◽  
Vol 62 (2) ◽  
pp. 214-219 ◽  
Author(s):  
Xuan Canh Nguyen ◽  
Won Woo Lee ◽  
Jin-Haeng Chung ◽  
So Yeon Park ◽  
Sook Whan Sung ◽  
...  

2010 ◽  
Vol 25 (2) ◽  
pp. 149-154 ◽  
Author(s):  
Gilles Mees ◽  
Christel Vangestel ◽  
Rudi Dierckx ◽  
Patrick Pauwels ◽  
Jan Van Meerbeeck ◽  
...  

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