Back to Search Start Over

IgG is involved in the migration and invasion of clear cell renal cell carcinoma.

Authors :
Zhengzuo Sheng
Yang Liu
Caipeng Qin
Zhenhua Liu
Yeqing Yuan
FengZhan Hu
Yiqing Du
Huaqi Yin
Xiaoyan Qiu
Tao Xu
Source :
Journal of Clinical Pathology; Jun2016, Vol. 69 Issue 6, p497-504, 8p, 1 Diagram, 2 Charts, 5 Graphs
Publication Year :
2016

Abstract

OBJECTIVE: To investigate if IgG can be expressed in clear cell renal cell carcinoma (cRCC), and the expression of IgG is involved in the cancer progression. If IgG expression can serve as a potential target in cancer therapies and be used for judging the prognosis. MATERIALS AND METHODS: By immunohistochemistry, we detected IgG in cRCC tissues (75 cRCC tissues and75 adjacent normal kidney tissues). Immunofluorescence and Western blot was used to detect the IgG in cRCC cell lines (786-0, ACHN and CAKI-I). By RT-PCR, the functional transcript of IgG heavy chain was detected. Knockdown of IgG was to analyze the proliferation, migration and invasion ability by CCK8, Transwell and Matrigel and apoptosis in cRCC cell lines. RESULTS: By immunohistochemistry, we found strong staining of IgG in 66 cases of 75 cRCC tissues and 63 cases of 75 adjacent normal kidney tissues. Immunofluorescence and Western blot was found IgG in cRCC cell lines. Knock-down IgG in cRCC cell lines resulted in significant inhibition of cell proliferation, migration and invasion, and the induction of apoptosis of the 786-0 cells. The immunohistochemistry analysis showed that high IgG expression significantly correlated with the poor differentiation and advanced stage of cRCC. CONCLUSION: IgG was over expressed in cRCC and was involved in the proliferation, migration and invasion of cancer cells. IgG expression may serve as a potential target in cancer therapies and could be used for judging the prognosis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219746
Volume :
69
Issue :
6
Database :
Complementary Index
Journal :
Journal of Clinical Pathology
Publication Type :
Academic Journal
Accession number :
115815769
Full Text :
https://doi.org/10.1136/jclinpath-2015-202881